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Studies about Snake Peptides: a Review about Brazilian Contribution

Abstract

The peptides present in snake venoms are studied because of their properties, constitutions, mechanisms of action and pharmacological potential. Recognizing this potential, the present study reports the contributions of Brazilian researchers about snake peptides, between 1975 and July 2020. Thus, this study serves as a basis for monitoring this theme in Brazil, referring to the trends and patterns of scientific production. The results indicated a significant increase in Brazilian scientific production over the years, highlighting institutions located in São Paulo state as, the Butantan Institute and University of São Paulo. The main journal where Brazilian authors publish their research is the Toxicon Journal. Collaborative networks were identified between Brazilian institutions and among other countries with Brazil. The most investigated species are found in brazilian territory, mainly those belonging to the genus Bothrops and the species Crotalus durissus. The increase in studies about this theme in Brazil is evident, however, a gap is highlighted for states outside the southeastern region and for other venomous species.

Keywords:
Biodiversity; Bioprospecting; Brazil; Reptiles; Scientific trend

HIGHLIGHTS

  • Brazilian scientific production on snake peptides has grown over the years.

  • São Paulo, is the most representative state in Brazil in research.

  • The main periodical where researches were published, is the Toxicon journal.

  • Collaboration is observed between institutions in Brazil and other countries.

HIGHLIGHTS

  • Brazilian scientific production on snake peptides has grown over the years.

  • São Paulo, is the most representative state in Brazil in research.

  • The main periodical where researches were published, is the Toxicon journal.

  • Collaboration is observed between institutions in Brazil and other countries.

INTRODUCTION

Snake poisons are mixtures of proteins and peptides with several biological activities [11 Bernardes CP, Santos NAG, Sisti FM, Ferreira RS, Santos-Filho NA, Cintra ACO, et al. A synthetic snake-venom-based tripeptide (Glu-Val-Trp) protects PC12 cells from MPP+ toxicity by activating the NGF-signaling pathway. Peptides. 2018;104:24-34.]. The toxins present in these compounds have pharmacological efficacy, especially antibacterial, considering the evidence observed in several studies [22 Almeida JR, Resende LM, Watanabe RK, Corassola VC, Huancahuire-Veja S, Caldeira CADS, et al. Snake venom peptides and low mass proteins: Molecular tools and therapeutic agentes. Curr Med Chem. 2017;24:3254-82.-33 Almeida JR, Mendes B, Lancelloti M, Marangoni S, Vale N, Passos O, et al. A novel synthetic peptide inspired on Lys49 phospholipase A 2 from Crotalus oreganus abyssus snake venom active against multidrug-resistant clinical isolates. Eur J Med Chem. 2018;149:248-56.]. Drugs produced from the active ingredients of snake toxins can be used to treat various diseases, including cardiovascular and cancer, as well as a pain relief and skin care [44 Vonk FJ, Jackson K, Doley R, Madaras F, Mirtschin PJ, Vidal N. Snake venom: From fieldwork to the clinic. BioEssays. 2011;33:269-79.-55 Remelli M, Brasili D, Guerrini R, Pontecchiani F, Potocki S, Rouwinska-Zyrek M, Watly J, et al. Zn(II) and Ni(II) complexes with poly-histidyl peptides derived from a snake venom. Inorganica Chim Acta. 2018;472:149-56.]. The crotamine peptide, found in snakes from genus Crotalus, performs a series of biological functions, such as antimicrobial and antitumor [66 Dal Mas C, Pinheiro DA, Campeiro JD, Mattei B, Oliveira V, Oliveira EB, et al. Biophysical and biological properties of small linear peptides derived from crotamine, a cationic antimicrobial/antitumoral toxin with cell penetrating and cargo delivery abilities. Biochim Biophys Acta Biomembr. 2017;1859:2340-9.]. It has also been reported that peptides extracted from Bothrops jararaca (Wagler 1824) were able to reduce blood pressure and improve renal function in hypertensive animals [77 Xavier CH, Miranda JRR, Yamaguchi J, Silveira KD, Teixeira MM, Chianca-Jr DA, et al. Bj-PRO-5a and Bj-PRO 10c Found at C-Type Natriuretic Peptide Precursor of Bothrops jararaca Change Renal Function of Hypertensive Rats. Int J Pept Res Ther. 2017;23:381-5.].

The snake venoms composition varies according to factors such as gender, family, species, geographic location, type of prey, age and size of the individual [88 Chippaux JP, Williams V, White J. Snake venom variability: Methods of study, results and interpretation. Toxicon. 1991;29:1279-303.-99 Sanhajariya S, Duffull SB, Isbister GK. Pharmacokinetics of Snake Venom. Toxins. 2018;10:73.]. Techniques called "omics", such as proteomics and transcriptomics, have enabled the understanding of the biochemistry and functionality of poisons, as well as their application in biotechnology, allowing the use of these poisons from drug development to agricultural application [1010 Zelanis A. Abordagens sistêmicas em toxinologia: Perspectivas e implicações de metodologias ômicas no estudo de toxinas de venenos de serpentes. Estud Biol Ambiente Divers. 2012;34:143-7.-1111 Oliveira AS, Fantinel AL, Artuzo FD, Oliveira L, Singer RB, Frota-Júnior MLC, et al. Applications of venom biodiversity in agriculture. EFB Bioeconomy Journal. 2021;100010.]. In Brazil, there are 392 species of snakes [1212 Madella-Auricchio CR, Auricchio P, Soares ES. Reptile species composition in the Middle Gurguéia and comparison with inventories in the eastern Parnaíba River Basin, State of Piauí, Brazil. Pap Avulsos Zool. 2017;57:375-86.] found in many habitats and niches [1313 Navega-Gonçalves MEC, Porto T. Conservação de serpentes nos biomas brasileiros [Snake conservation in Brazilian biomes]. Bioikos. 2016;30: 55-76.]. In Brazil, researches were carried out and discovered the bradykinin in B. jararaca venom in 1949 [1414 Rocha e Silva M, Beraldo WT, Andrade SO. A new factor (Bradykinin) released from plasma globulin by snake venom and trypsin. Procedures of the First International Congress of Biochemistry. 1949;119.] and, later, bradykinin-potentiating peptides in the 1960s [1515 Ferreira SH. A bradykinin-potentiating factor (BPF) present in the venom of Bothrops jararaca. Br J Pharmacol. 1965;24:163-9.], that allowed the creation of the drug captopril [1616 Ferreira SH. Aspectos históricos da hipertensão [Historical aspects of hypertension]. HiperAtivo. 1998;5:230-232.] used to treat arterial hypertension. The Butantan Institute is the main immunobiological producer in the country, developing diverse projects about composition and action of snake venoms and assisting in the new drugs development, according to the official website of the institute (https://butantan.gov.br/institutional/o-instituto).

Researches about snake peptides as pharmacological agents, especially in developing countries such Brazil, are important, since in these countries infectious diseases are a major cause of death due to the indiscriminate use of antibiotics [1717 Santos-Filho NA, Fernandes RS, Sgardiloi BF, Ramos MAS, Piccoli JP, Camargo IBC, et al. Antibacterial Activity of the Non-Cytotoxic Peptide (p-BthTX-I)2 and Its Serum Degradation Product against Multidrug-Resistant Bacteria. Molecules. 2017;22:1898.]. Thus, antimicrobial peptides from snakes have been studied as an alternative treatment to these diseases, since they have already demonstrated efficacy against fungi [66 Dal Mas C, Pinheiro DA, Campeiro JD, Mattei B, Oliveira V, Oliveira EB, et al. Biophysical and biological properties of small linear peptides derived from crotamine, a cationic antimicrobial/antitumoral toxin with cell penetrating and cargo delivery abilities. Biochim Biophys Acta Biomembr. 2017;1859:2340-9.,1818 Maluf SEC, Dal Mas C, Oliveira EB, Melo PM, Carmona AK, Gazarini ML, et al. Inhibition of malaria parasite Plasmodium falciparum development by crotamine, a cell penetrating peptide from the snake venom. Peptides. 2016;78:11-6.] and bacteria [1717 Santos-Filho NA, Fernandes RS, Sgardiloi BF, Ramos MAS, Piccoli JP, Camargo IBC, et al. Antibacterial Activity of the Non-Cytotoxic Peptide (p-BthTX-I)2 and Its Serum Degradation Product against Multidrug-Resistant Bacteria. Molecules. 2017;22:1898.,1919 Sulca MA, Remuzgo C, Cardenas J, Kiyota S, Cheng E, Bemquerer MP, et al. Venom of the Peruvian snake Bothriopsis oligolepis: Detection of antibacterial activity and involvement of proteolytic enzymes and C-type lectins in growth inhibition of Staphylococcus aureus. Toxicon. 2017;134: 30-40.].

In this sense, the objective of this study was to track the scientific production in Brazil about peptides from snake venoms, to evidence (i) the time trend of papers produced in the country from the most remote year of the databases until July 2020; (ii) the geographic aspect of studies in the country; (iii) the institutions to which the authors and co-authors of these studies were linked; (iv) the journal where these papers were published; (v) collaboration networks between institutions; (vi) the countries which Brazilian researchers had partnerships and (vii) the main species studied.

MATERIAL AND METHODS

Data collection

In this study, was reviewed the literature that addresses snake peptides published by researchers (including first authors and co-authors) linked to Brazilian institutions until July 2020. The full articles, reviews and short communications were searched on the ISI Web of Science and Scopus databases with the keywords: “snakes” and “peptides”. Papers that did not address snake peptides, whose authors institutions were not located in Brazil, and in which the complete paper was not found were discarded.

For each paper found were investigated: (i) the year of publication, (ii) geographic aspect of the research (state of the country where the educational institution whose Brazilian authors and/or co-authors were linked during the execution of the research (iii) the institutions to whose Brazilian authors and/or co-authors were linked during the execution of the research, (iv) the journals in which the papers were published, (v) the collaborations between different institutions in the studies (vi) the collaborations of authors and/or co-authors linked to institutions in other countries and (vii) the investigated species of snakes.

Data analysis

The increase of published papers was calculated using Pearson's correlation coefficient (p <0.05) between year and number of published articles. The data of Brazilian states and institutions that most contributed, as well as the journals where Brazilian’s scientists most published, are shown in the form of proportion. Collaboration networks between Brazilian institutions and among other countries with Brazil were built using the VOSviewer software. To analyze collaboration between institutions, the minimum number of documents by organization was four collaborations. To analyze collaboration between countries, the minimum number of publications by country was one. Because of the divergence in the way that the names of institution are written in papers, the names of the institutions were unified.

RESULTS

Temporal and geographical aspect

The search on the Web of Science returned 2209 papers published since 1967. The Scopus database returned 5367 documents published since 1952. Considering the two databases, 592 studies had the participation of researchers linked to Brazilian institutions. After evaluating the criteria, 451 were selected for data analysis. Among these, researchers from Brazilian institutions were the main authors in approximately 84% of the studies (n = 380) and co-authors, led by foreigners, in approximately 15% (n = 71). The first paper found, according to the criteria, dates to 1975, increasing until July 2020 (r = 0.91; p <0.001; Figure 1). Scientific collaboration was registered in institutions in 20 states in Brazil, out of 27 in the country (Figure 2). Considering the regions of all authors, the most representative institutions are located mainly in the state of São Paulo, which has been the driving force with approximately 72% of the studies (n = 326), followed by Minas Gerais 17% (n = 78) and Rio de Janeiro, whose institutions contributed with 13% (n = 60). The others Brazilian states contributed with about 6.19% (n = 28) of total production.

Figure 1
Number of published papers about snake peptides with the participation of Brazilian researchers between 1975 and July 2020.

Figure 2
Representativeness of the Brazilian states’ contribution in studies about snake peptides.

Main institutions, journals and collaboration networks

The contribution of 91 Brazilian institutions in the papers was recorded. More than 40% of the 451 papers had the participation of Butantan Institute (n = 184). Two other representative institutions were the University of São Paulo (USP) with 30% (n = 137) and the Federal University of São Paulo (UNIFESP) with 13% (n = 60). It is also important to highlight other Brazilian institutions such as the State University of São Paulo “Júlio de Mesquita Filho” (UNESP) (n = 49) and the State University of Campinas (UNICAMP) (n = 40), as well as the Oswaldo Cruz Foundation (FIOCRUZ) (n = 38), the Ezequiel Dias Foundation (FUNED) (n = 36), the Federal University of Rio de Janeiro (UFRJ) (n = 32), the Federal University of Minas Gerais (UFMG) (n = 28) and the Federal University of Ceará (UFC) (n = 24). The other institutions together (n = 81) accounted for about 67% of the papers (n = 303).

The 451 researches were published in 127 journals, whose Toxicon journal holds the largest number of papers, 24.8% (n = 112). Next are the journals, Comparative Biochemistry and Physiology with 4.4% (n = 20), Journal of Venomous Animals and Toxins Inclusing Tropical Diseases with 4.2% (n = 19), Journal of Proteomics (3.5%, n = 16), Toxins (3.5%, n = 16), Archives of Biochemistry and Biophysics (2.8%, n = 13), Biochimie (2.8%, n = 13), Peptides (2.8%, n = 13), Journal of Proteome Research (2.6%, n = 12) and Biochimica et Biophysica Acta (2.4% n = 11). Other journals together account for about 45% (n = 206).

Several collaboration networks were observed between institutions in Brazil (Figure 3), as well as the collaboration of institutions outside the country, such as the United States, Germany, Japan, France and Spain (Figure 4).

Figure 3
Collaboration network between Brazilian institutions involved in studies about snake peptides. Federal University of Pernambuco (UFPE), State University of Ceará (UECE), Federal University of São João del-Rei (UFSJ), Institute for Energy and Nuclear Research (IPEN), Federal University of Rio Grande do Sul (UFRS), State University of Rio de Janeiro (UERJ), University of Ribeirão Preto (UNAERP), Federal University of Santa Catarina (UFSC), Federal University of Uberlândia (UFU), Federal University of Paraná (UFPR), Univesity of Brasília (UNB), Catholic University of Brasília (UCB).

Figure 4
Collaboration among between Brazil and other countries in studies about snake peptides.

Species investigated

A total of 92 species were investigated in different studies involving the antibacterial, antihypertensive, antifungal, antitumor potential, as well as its use for antiophidic serum production and its peptides. About 25% (n = 116) of the papers evaluated the Bothrops jararaca species, while approximately 21% (n = 96) studied Crotalus durissus (Linnaeus 1758) and 7% (n = 33) used Bothrops jararacussu (Lacerda 1884). Considering that many studies used more than one species, other species were investigated in 79.15% of the papers (n = 357). Approximately 9.31% (n = 42) of the papers did not specify the used species or were review papers. Table 1 shows the number of studies with the most cited species.

Table 1
Most investigated snake species in studies on peptides published with the collaboration of Brazilian.

DISCUSSION

Temporal and geographical aspect

The first study found in the databases dates from 1975 and it evaluated bradykinin-potentiating peptides in the venom of B. jararaca and Gloydius blomhoffii (Boie 1826) (referred in the article as Agkistrodon halys blomhoffii), being the latter, geographically distributed in Japan, China and Russia. The study evaluated the relationship between the structure and activity of synthetic peptides in guinea pig (Cavia porcellus) and in female rats [2020 Tominaga M, Stewart JM, Paiva TB, Paiva ACM. Synthesis and properties of new bradykinin potentiating peptides. Eur J Med Chem. 1975;18:130-3.]. From then on, until the 1990s, few studies were published by Brazilian researchers, most of them linked to the Butantan Institute and USP using the species B. jararaca [2121 Lavras AC, Fichman M, Hiraichi E, Boucault MA, Tobo T. Components of the renin-angiotensin system in the plasma of Bothrops jararaca. Agents Actions. 1978;8:141-5.-2222 Mandelbaum FR, Reichel AP, Assakura MT. Isolation and characterization of a proteolytic enzyme from the venom of the snake Bothrops jararaca (Jararaca). Toxicon. 1982;20:955-72.]. An increase in the number of papers begins to be observed from 1990 when the first works of researchers linked to institutions of Goiás [2323 Silva JN, Griffin PR, Aird SD. Comparative chromatography of Brazilian coral snake (Micrurus venoms). Comp Biochem Physiol B Biochem Mol Biol. 1991;100:117-26.], Minas Gerais [2424 Sanchez EF, Diniz CR, Richardson M. The complete amino acid sequence of the haemorrhagic factor LHFII, a metalloproteinase isolated from the venom of the bushmaster snake (Lachesis muta muta). FEBS Letters. 1991;282: 178-82.], Rio de Janeiro [2525 Fernandes PD, Guimarães JA Assreuy J. Comparative effects of two potentiating peptides (KPP and BPP9a) on kinin-induced rat paw edema. Agents Actions. 1991;32:182-7.] and Rio Grande do Sul states [2626 Jerusalinsky D, Cerveñansky C, Walz R, Bianchin M, Izquierdo I. A peptide muscarinic toxin from the Green Mamba venom shows agonist-like action in an inhibitory avoidance learning task. Eur J Pharmacol. 1993;240:103-5.] were published. Among the papers published in this decade, there is a study with the poison of C. durissus, with the crotoxin purification [2727 Perales J, Villela C, Domont GB, Choumet V, Saliou B, Moussatché H, et al. Molecular structure and mechanism of action of the crotoxin inhibitor from Crotalus durissus terrificus serum. Eur J Biochem. 1995;227:19-26.], and with the crotamine potential to act as an analgesic [2828 Mancin AC, Soares AM, Andrião-Escarso SH, Faça VM, Greene LJ, Zuccolotto S, et al. The analgesic activity of crotamine, a neurotoxin from Crotalus durissus terrificus (South American rattlesnake) venom: A biochemical and pharmacological study. Toxicon. 1998;36:1927-37.].

The increase in the number of papers with the collaboration of Brazilians is more evident in the 2000s. Until the beginning of the decade, the peptides from coral snake (M. corallinus) venom had been little studied. Brazilian researchers have contributed to the reduction of this gap by analyzing, cloning and characterizing components of the toxins of this species, including peptides [2929 Oliveira JS, Silva ÁRBP, Soares MB, Stephano MA, Dias WO, Raw I, et al. Cloning and Characterization of an α-Neurotoxin-Type Protein Specific for the Coral Snake Micrurus corallinus. Biochem Biophys Res Commu. 2000;267:887-91.-3030 Oliveira UC, Assui A, Silva ÁRBP, Oliveira JS, Ho PL. Cloning and characterization of a basic phospholipase A2 homologue from Micrurus corallinus (Coral snake) venom gland. Toxicon. 2003;42: 249-55.]. There are also studies that have identified new bradykinin-potentiating peptides in the venom of B. jararaca [3131 Ianzer D, Konno K, Marques-Porto R, Vieira Portaro FC, Stöcklin R, Martins de Camargo AC, et al. Identification of five new bradykinin potentiating peptides (BPPs) from Bothrops jararaca crude venom by using electrospray ionization tandem mass spectrometry after a two-step liquid chromatography. Peptides. 2004;25:1085-92.] and studies that used these peptides to develop drugs against hypertension, since bradykinin is involved in blood pressure control and other physiological processes [3232 Fernandez JH, Neshich G, Camargo AC. Using bradykinin-potentiating peptide structures to develop new antihypertensive drugs. Genet Mol Res. 2004;3:554-63.]. In addition, Gomes and coauthors [3333 Gomes VM, Carvalho AO, Da Cunha M, Keller MN, Bloch C, Deolindo P, et al. Purification and characterization of a novel peptide with antifungal activity from Bothrops jararaca venom. Toxicon. 2005;45:817-27.] isolated a new peptide from the snake B. jararaca with inhibitory function against phytopathogenic fungi like Fusarium oxysporum and Colletotrichum lindemuthianum and yeasts like Candida albicans and Saccharomyces cerevisiae.

Rizzi and coauthors [3434 Rizzi CT, Carvalho-de-Souza JL, Schiavon E, Cassola AC, Wanke E, Troncone LRP. Crotamine inhibits preferentially fast-twitching muscles but is inactive on sodium channels. Toxicon. 2007;50:553-62.] demonstrated that the crotamine from C. durissus poison preferentially inhibits fast muscles, however, the authors claim that the sodium channels would not be the targets of this peptide toxin, as was believed before. Regarding bradykinin-potentiating biomolecules, Rioli and coauthors [3535 Rioli V, Prezoto BC, Konno K, Melo RL, Klitzke CF, Ferro ES, et al. A novel bradykinin potentiating peptide isolated from Bothrops jararacussu venom using catallytically inactive oligopeptidase EP24.15. FEBS J. 2008; 275:2442-54.] identified a new B. jararacussu peptide with the potential to induce arterioles vasodilation with little increase in leukocyte flow. Cardoso and coauthors [3636 Cardoso R, Homsi-Brandeburgo MI, Rodrigues VM, Santos WB, Souza GLR, Prudencio CR, et al. Peptide mimicking antigenic and immunogenic epitope of neuwiedase from Bothrops neuwiedi snake venom. Toxicon. 2009; 53:254-61.] found peptides with immunogenic activity against toxins from the snake venom of B. neuwiedi, contributing with another possibility of protection in case of poisoning by that snake. In addition to these works, Martins and coauthors [3737 Martins NM, Ferreira DAS, Carvalho Rodrigues MA, Cintra ACO, Santos NAG, Sampaio SV, et al. Low-molecular-mass peptides from the venom of the Amazonian viper Bothrops atrox protect against brain mitochondrial swelling in rat: Potential for neuroprotection. Toxicon. 2010;56:86-92.] studying the B. atrox venom, detected peptides with neuroprotective function acting against mitochondrial swelling in the brain of rats, contributing to strategies for treatment against neurodegenerative diseases.

In the last decade, there has been a significant participation of Brazilian institutions in the studies found. Among them, the study by Martins-Santos and coauthors [3838 Martins-Santos MES, Resende RR, Pinto FCH, Soares AM, Marangoni S, Oliveira E, et al. Effect of a Pool of Peptides Isolated from Crotalus durissus terrificus (South American Rattlesnake) Venom on Glucose Levels of Mice Fed on a High-Fat Diet. Int J Pept Res Ther. 2011;17:225-230.] investigated the effect of a mixture of peptides from C. durissus on glucose concentration in rats fed a high-fat diet and showed a reduction in glycemia as well as in the glucose concentration in blood. Silva and coauthors [3939 Silva SL, Almeida JR, Resende LM, Martis W, Henriques FAFA, Baldasso PA, et al. Isolation and characterization of a natriuretic peptide from Crotalus oreganus abyssus (grand canyon rattlesnake) and its effects on systemic blood pressure and nitrite levels. Int J Pept Res Ther. 2011;17:165-73.] isolated and characterized a peptide from Crotalus oreganus showing its properties in the blood pressure regulation. A study with Bothropoides mattogrosensis venom, detected peptide fragments with anti-microbial activity in the enzyme L-amino oxidase, suggesting these as candidates for new antibiotic projects [4040 Okubo BM, Silva ON, Migliolo L, Gomes DG, Porto WF, Batista CL, et al. Evaluation of an Antimicrobial L-Amino Acid Oxidase and Peptide Derivatives from Bothropoides mattogrosensis Pitviper Venom. PLoS ONE. 2012;7:e33639.]. Another study with bradykinin-potentiating peptides from B. jararaca, showed that they induce morphological changes in the seminiferous tubules of rats, impairing spermatogenesis, however, the same was not observed when the animals were exposed to the captopril medication, derived from these peptides [4141 Gilio JM, Portaro FC, Borella MI, Lameu C, Camargo AC, Alberto-Silva C. A bradykinin-potentiating peptide (BPP-10c) from Bothrops jararaca induces changes in seminiferous tubules. J Venom Anim Toxins Incl Trop Dis. 2012;19:28.]. Martins and coauthors [4242 Martins NM, Santos NA, Sartim MA, Cintra AC, Sampaio SV, Santos AC. A tripeptide isolated from Bothrops atrox venom has neuroprotective and neurotrophic effects on a cellular model of Parkinson's disease. Chem Biol Interact. 2015;235:10-6.] isolated a peptide from B. atrox venom with neuroprotective activity that can be effective as a therapeutic strategy for Parkinson's disease.

Dal Mas and coauthors [4343 Dal Mas C, Moreira JT, Pinto S, Monte GG, Nering MB, Oliveira EB, et al. Anthelmintic effects of a cationic toxin from a South American rattlesnake venom. Toxicon. 2016;116:49-55.] reported that in addition to antimicrobial and antitumor activity, crotamine has unique cell penetrating properties with affinity for acidic vesicles, and anthelmintic potential, proposing a way to overcome drug resistance. Cavalcante and coauthors [4444 Cavalcante C, Falcão C, Fontenelle R, Andreu D, Rádis-Baptista G. Anti-fungal activity of Ctn[15-34], the C-terminal peptide fragment of crotalicidin, a rattlesnake venom gland cathelicidin. J Antibiot. 2017;70:231-7.] detected antifungal activity of C. durissus crotalicidine, pointing out that it is a promising clue for treatment of fungal diseases. One year later, Bandeira and coauthors [4545 Bandeira ICJ, Bandeira-Lima D, Mello CP, Pereira TP, Menezes RRPPB, Sampaio TL, et al. Antichagasic effect of crotalicidin, a cathelicidin-like vipericidin, found in Crotalus durissus terrificus rattlesnake's venom gland. Parasitology. 2018;145:1059-64.] found that crotalicidine has an effect against Chagas disease, contributing to the possible development of agents against this disease. More recently, a study with B. moojeni snake identified a peptide derived from a metalloprotease with an inhibitory action on the survival of Plasmodium falciparum, that causes malaria [4646 Martins GG, Holanda RHJ, Alfonso J, Garay AFG, Santos APZ, Lima AM, et al. Identification of a peptide derived from a Bothrops moojeni metalloprotease with in vitro inhibitory action on the Plasmodium falciparum purine nucleoside phosphorylase enzyme (PfPNP). Biochimie. 2019;162:97-106.]. In addition, Oliveira and coauthors [4747 Oliveira NGJ, Cardoso MH, Velikova N, Giersbers M, Wells JM, Rezende TMB, et al. Physicochemical-guided design of cathelicidin-derived peptides generates membrane active variants with therapeutic potential. Sci Rep. 2020;10:9127.] described the antimicrobial activities against a diversity of microorganisms, the action modes and structure of new peptides from C. durissus. It is important to highlight that, over the years, studies by Brazilian researchers have also shown that the study of the composition of snake venoms, including peptides, can be applied beyond pharmacology, for example, to understand the evolutionary relationships between different snake species and their distribution pattern throughout evolution [4848 Fusco LS, Neto EB, Francisco AF, Alfonso J, Soares A, Pimenta DC, et al. Fast venomic analysis of Crotalus durissus terrificus from northeastern Argentina. Toxicon: X. 2020;100047.]. About these applications, currently, the development of biopesticides for agricultural use from snake venom has also been studied [1111 Oliveira AS, Fantinel AL, Artuzo FD, Oliveira L, Singer RB, Frota-Júnior MLC, et al. Applications of venom biodiversity in agriculture. EFB Bioeconomy Journal. 2021;100010.]. It is important to highlight that proteomics techniques were used in most studies, that is, venom components such as proteins and peptides were separated, identified and characterized through techniques such as chromatography, electrophoresis and phylogenetic analysis [4949 Terra RMS, Pinto AFM, Guimarães JA, Fox JW. Proteomic profiling of snake venom metalloproteinases (SVMPs): Insightsinto venom induced pathology. Toxicon. 2009;54:836-44.-5050 Viala VL, Hildebrand D, Fucase TM, Sciani JM, Prezotto-Neto JP, Riedner M, et al. Proteomic analysis of the rare Uracoan rattlesnake Crotalus vegrandis venom: Evidence of a broad arsenal of toxins. Toxicon. 2015;107:234-51.]. The knowledge gained from the use of proteomics (and other approaches such as genomics) allows the development of biotechnology from biological resources such as snake venoms to create more sustainable solutions for agriculture such as new crop varieties and biopesticides [1111 Oliveira AS, Fantinel AL, Artuzo FD, Oliveira L, Singer RB, Frota-Júnior MLC, et al. Applications of venom biodiversity in agriculture. EFB Bioeconomy Journal. 2021;100010.].

Most of the studies had the collaboration of at least one author linked to institutions located in São Paulo, which mean that the five institutions that most contributed to studies are located in this state. This tendency of scientific production in Brazil to be concentrated in the southeast region has been pointed out by reviews published in several areas such as health and biological sciences [5151 Zorzetto R, Razzouk D, Dubugras MTB, Gerolin J, Schor N, Guimarães JA, et al. The scientific production in health and biological sciences of the top 20 Brazilian universities. Braz J Med Biol Res. 2006;39:1513-20.-5252 Luchs A. Profile of Brazilian scientific production on A/H1N1 pandemic influenza. Cien Saúde Colet. 2012;17:1629-34.], dentistry [5353 Tarazona B, Vidal-Infer A, Alonso-Arroyo A. Bibliometric analysis of the scientific production in implantology (2009-2013). Clin Oral Implants Res. 2016;28:864-70.], education [5454 Coutinho RX, Dávila ES, dos Santos WM, Rocha JBT, Souza DOG, Folmer V, et al. Brazilian scientific production in science education. Scientometrics. 2012;92:697-710.], renewable energies [5555 Manzano-Agugliaro F, Alcayde A, Montoya FG, Zapata-Sierra A, Gil C. Scientific production of renewable energies worldwide: An overview. Renew Sustain Energy Rev. 2013;18:134-43.] and pharmaceutical care [5656 Funchal-Witzel MDR, Castro LLC, Romano-Lieber NS, Narvai PC. Brazilian scientific production on pharmaceutical care from 1990 to 2009. Braz J Pharm Sci. 2011;47:409-20.]. According to a study by the Industries Federation of Ceará State (FIEC) in 2018, São Paulo is the state of Brazil that is in the first place in the ranking of capabilities that most invest in infrastructure and communications, public investment in science and technology, quality of graduate studies and insertion of masters and doctors in the industry. At the same time, the state ranks second in the index that considers scientific publications, global competitiveness in technological sectors, technological intensity of the productive structure and intellectual property in industry. The survey shows, therefore, that São Paulo state is a leader in public investment in science, followed by other states in the southeastern region such as Rio de Janeiro and Minas Gerais that occupy the fourth and seventh place, respectively. In the south region are Paraná and Rio Grande do Sul, which occupy, respectively, the second and fifth place, while the Federal District, in the central-west region, occupies the third position of the ranking. It is also important to note that São Paulo is the state with the highest gross national product (GNP) in the country according to IBGE (Brazilian Institute of Geography and Statistics) and that, historically, there has been a continuous investment in research and development, which can explain the concentration of scientific production in that state [5252 Luchs A. Profile of Brazilian scientific production on A/H1N1 pandemic influenza. Cien Saúde Colet. 2012;17:1629-34.].

Main institutions, journals and collaboration networks

The Butantan Institute, a leader in contributing to studies in Brazil, is an institution that was born in 1901 in the state of São Paulo with to produce serum against bubonic plague [5757 Franco M, Kalil J. The Butantan Institute: History and Future Perspectives. PLOS Negl Trop Dis. 2014;8:e2862.]. Over the years, the institute has become one of the main scientific institutions in Brazil, known worldwide for studying the toxins of venomous animals, in addition to projects related to vaccines production, which attracted the attention of several international institutions for establishment of partnerships [5757 Franco M, Kalil J. The Butantan Institute: History and Future Perspectives. PLOS Negl Trop Dis. 2014;8:e2862.]. In relation to snakes, from the research carried out by the institution, various serums are produced, such as antibotropic, anticrotalic and antielapidic, which are made available to the population free of charge through the Health Ministry (see the Institute's website). In addition, the Butantan Institute is made up of 35 scientific laboratories, a center for technological innovation, a hospital specializing in treating victims of accidents with venomous animals, animal houses for snakes and other venomous animals and a team of researchers, including professionals, masters, doctoral and postdoctoral students [5858 Corrêa-Junior MC, Maria DA, Moura-da-Silva AM, Pizzocaro KF, Ruiz IR. Inhibition of melanoma cells tumorigenicity by the snake venom toxin jararhagin. Toxicon. 2002;40:739-48.].

Thus, the research demonstrates the importance of the institution in Brazilian scientific production, contributing from the first studies found in the databases to the most recent ones. Among them, there are studies about constitution, characterization and therapeutic potential of components from venom of B. jararaca [2121 Lavras AC, Fichman M, Hiraichi E, Boucault MA, Tobo T. Components of the renin-angiotensin system in the plasma of Bothrops jararaca. Agents Actions. 1978;8:141-5.-2222 Mandelbaum FR, Reichel AP, Assakura MT. Isolation and characterization of a proteolytic enzyme from the venom of the snake Bothrops jararaca (Jararaca). Toxicon. 1982;20:955-72., 5858 Corrêa-Junior MC, Maria DA, Moura-da-Silva AM, Pizzocaro KF, Ruiz IR. Inhibition of melanoma cells tumorigenicity by the snake venom toxin jararhagin. Toxicon. 2002;40:739-48.

59 Zelanis A, Andrade-Silva D, Rocha MM, Furtado MF, Serrano SM, Junqueira-de-Azevedo IL, et al. A transcriptomic view of the proteome variability of newborn and adult Bothrops jararaca snake venoms. PLoS Negl Trop Dis. 2012; 6:e1554.
-6060 Menezes MC, Kitano ES, Bauer VC, Oliveira AK, Cararo-Lopes E, Nishiyama-Jr MY, et al. Early response of C2C12 myotubes to a sub-cytotoxic dose of hemorrhagic metalloproteinase HF3 from Bothrops jararaca venom. J Proteomics. 2019;198:163-76.], C. durissus [3434 Rizzi CT, Carvalho-de-Souza JL, Schiavon E, Cassola AC, Wanke E, Troncone LRP. Crotamine inhibits preferentially fast-twitching muscles but is inactive on sodium channels. Toxicon. 2007;50:553-62., 6161 Giorgi R, Bernardi MM, Cury Y. Analgesic effect evoked by low molecular weight substances extracted from Crotalus durissus terrificus venom. Toxicon. 1993;31:1257-65.

62 Oguiura N, Boni-Mitake M, Rádis-Baptista G. New view on crotamine, a small basic polypeptide myotoxin from South American rattlesnake venom. Toxicon. 2005;46:363-70.

63 Brigatte P, Faiad OJ, Ferreira Nocelli RC, Landgraf RG, Palma MS, Cury Y, et al. Walker 256 Tumor Growth Suppression by Crotoxin Involves Formyl Peptide Receptors and Lipoxin A4. Mediators Inflamm. 2016;2016:1-11.
-6464 Mambelli-Lisboa NC, Sciani JM, Silva ARBP, Kerkis I. Co-Localization of Crotamine with Internal Membranes and Accentuated Accumulation in Tumor Cells. Molecules. 2018;23:968.] among several other snake species.

Another significant institution that collaborate with studies is the University of São Paulo, USP. According to the 2019 Clarivate Analytics company report, USP is the most productive Brazilian university in all sectors of science (Health Sciences, Biological Sciences, Exact and Natural Sciences, Agricultural Sciences and Engineering), followed by UNESP and UNICAMP. Historically, greater investment in research has been observed through public and private sectors in São Paulo, in addition to the presence of an important development agency, the São Paulo State Research Support Foundation (FAPESP), which have been pointed as the justification for concentrated scientific production in São Paulo universities [5151 Zorzetto R, Razzouk D, Dubugras MTB, Gerolin J, Schor N, Guimarães JA, et al. The scientific production in health and biological sciences of the top 20 Brazilian universities. Braz J Med Biol Res. 2006;39:1513-20.]. Other important health institutions in Brazil were FIOCRUZ and FUNED. Among its lines of research, FIOCRUZ has studies related to toxicology and the production of antibiotics, anti-inflammatories, analgesics, in addition to medicines for diseases of nervous system, hypertension and diabetes, according to the official website of the institution. FUNED is also one of the references in the research of snake venoms in Brazil. Regarding patent registrations, a search of the EPO patent database (worldwide.espacenet.com) shows that researchers from the Federal University of São Carlos, FAPESP and the UERJ have patented synthetic peptide derived from alternagin-C of B alternatus, other patent records are found for FIOCRUZ (combination of crotamine from C. durissus and drugs for the treatment of leishmaniasis), for UFMG with the use of formulation containing crotoxin for the treatment of muscle dystonias, among other records.

In relation to the journals where the researches were published, there is a large volume of papers in the Toxicon Journal. This journal, currently with an impact factor of 2.201, aims to publish papers related to toxins from animals, plants and microorganisms, in particular chemical, pharmacological, toxicological and immunological properties of these toxins, in addition to clinical observations on poisoning. These papers had focus on antibacterial, antitumor and analgesic activities, among others. Also, at the time of this research, this journal accepts full research articles, short communications, letters to the editor, announcements, reviews, mini-reviews and clinical reports. Among the studies published in this journal, there are works dating from the 1980s, featuring components of the B. jararaca venom [2222 Mandelbaum FR, Reichel AP, Assakura MT. Isolation and characterization of a proteolytic enzyme from the venom of the snake Bothrops jararaca (Jararaca). Toxicon. 1982;20:955-72.], hemorrhagic factors of B. neuwiedi [6565 Mandelbaum FR, Assakura MT, Reichl AP. Characterization of two hemorrhagic factors isolated from the venom of Bothrops neuwiedi (Jararaca pintada). Toxicon. 1984;22:193-206.], a study with the snake B. moojeni [6666 Assakura MT, Reichl AP, Asperti MCA, Mandelbaum FR. Isolation of the major proteolytic enzyme from the venom of the snake Bothrops moojeni (Caissaca). Toxicon. 1985;23:691-706.] and evaluation of Naja naja peptide [6767 Castro VRO, Vernon LP. Hemolytic activity of thionin from Pyrularia pubera nuts and snake venom toxins of Naja naja species: Pyrulariathionin and snake venom cardiotoxin compete for the same membrane site. Toxicon. 1989;27:511-7.]. Over the years, papers have been published evaluating the venom hemorrhagic factors of the snake Lachesis muta [6868 Sanchez EF, Cordeiro MN, De-Oliveira EB, Juliano L, Prado ES, Diniz CR. Proteolytic specificity of two hemorrhagic factors, LHF-I and LHF-II, isolated from the venom of the bushmaster snake (Lachesis muta muta). Toxicon. 1995;33: 1061-9.], the renal toxicity of the venom from B. moojeni snake [6969 Barbosa PS, Havt A, Facó PE, Sousa TM, Bezerra ISAM, Fonteles MC, et al. Renal toxicity of Bothrops moojeni snake venom and its main myotoxins. Toxicon. 2002;40:1427-35.], the action mechanisms of crotamine peptide [3434 Rizzi CT, Carvalho-de-Souza JL, Schiavon E, Cassola AC, Wanke E, Troncone LRP. Crotamine inhibits preferentially fast-twitching muscles but is inactive on sodium channels. Toxicon. 2007;50:553-62.] and the urinary metabolites of B. jararaca bradykinin-potentiating peptides in mice [7070 Silva CA, Ianzer DA, Portaro FCV, Konno K, Faria M, Fernandes BL, et al. Characterization of urinary metabolites from four synthetic bradykinin potentiating peptides (BPPs) in mice. Toxicon. 2008;52: 501-7.]. More recently, there is a study about the poison of B. jararaca [7171 Querobino SM, Costa MS, Alberto-Silva C. Protective effects of distinct proline-rich oligopeptides from B. jararaca snake venom against oxidative stress-induced neurotoxicity. Toxicon. 2019;167:29-37.], in addition to others.

Another important journal pointed out is Comparative Biochemistry and Physiology, a journal divided between parts A (Molecular and Integrative Physiology), B (Biochemistry and Molecular Biology), C (Toxicology and pharmacology) and D (Genomics and Proteomics). Most studies were published in part C of the journal (n = 10 studies, 50% of the total of 20 studies published in the journal). The scope of this journal is the toxicological mechanisms at different levels of organization, mainly molecular assessments of the xenobiotic’s mechanisms of action on the organism physiology. Among the studies published by this journal are research about a new peptide in the poison of C. durissus [7272 Higuchi S, Murayama N, Saguchi K, Ohi H, Fujita Y, da Silva NJ, et al. A novel peptide from the ACEI/BPP-CNP precursor in the venom of Crotalus durissus collilineatus. Comp Biochem Physiol C Toxicol Pharmacol. 2006;144:107-21.], on endothelin, vasoactive peptides, and the differences in their receptors in B. jararaca and Oxyrhopus guibei snakes [7373 Mesquita LS, Frias FT, Carmona E, Borgheresi RA. Differences in endothelin receptor types in the vasculature of Bothrops jararaca (Viperidae) and Oxyrhopus guibei (Colubridae) snakes. Comp Biochem Physiol C Toxicol Pharmacol. 2008;148:61-7.]. There was also great prominence in the work about vasoactive peptides isolated from B. jararaca plasma [7474 Barreto SA, Chaguri LCAG, Prezoto BC, Lebrun I. Effects of three vasoactive peptides isolated from the plasma of the snake Bothrops jararaca. Comp Biochem Physiol C Toxicol Pharmacol. 2009;149:552-8.], a study about biochemical characterization of Pseudoboa neuwiedii venom [7575 Torres-Bonilla KA, Andrade-Silva D, Serrano SMT, Hyslop S. Biochemical characterization of venom from Pseudoboa neuwiedii (Neuwied’s false boa; Xenodontinae; Pseudoboini). Comp Biochem Physiol C Toxicol Pharmacol. 2018;213:27-38.] and the discovery of cardioprotective effects of alternagin-C, a peptide from B. alternatus snake [7676 Monteiro DA, Kalinin AL, Selistre-de-Araújo HS, Nogueira LAN, Beletti ME, Fernandes MN, et al. Cardioprotective effects of alternagin-C (ALT-C), a disintegrin-like protein from Rhinocerophis alternatus snake venom, on hypoxia-reoxygenation-induced injury in fish. Biochem Physiol C Toxicol Pharmacol. 2019;215:67-75.].

As for collaboration networks, there are many works carried out in partnership by researchers from different Brazilian institutions. The Butantan Institute and USP show an expressive network of collaboration with institutions from different regions of Brazil. In addition to these, institutions such as UNIFESP, UFMG and UFRJ also showed interinstitutional partnerships. Partnerships between research institutes such as Vital Brazil Institute and Pasteur Institute and universities are noted. However, it is observed that the collaboration networks are predominantly formed by institutions located in the southeast region. These partnerships between researchers from different areas and institutions are important for science development in country, since they can assist to obtain faster results and, therefore, in the development of research [7777 Hilário CM, Grácio MCC. Scientific collaboration in Brazilian researches: a comparative study in the information science, mathematics and dentistry fields. Scientometrics, 2017;113:929-50.].

Although collaboration networks have been observed in studies about snake peptides, the low participation of institutions in other regions should be considered. A similar result is pointed out by reviews that highlighted the collaboration between Brazilian researchers, showing a predominance of institutions located in the southeastern and southern regions [7878 Gheno EM, Rosemberg DB, Souza DO, Calabró L. Zebrafish in Brazilian Science: Scientific Production, Impact, and Collaboration. Zebrafish. 2016;13:217-25.]. As for international collaboration, Brazilian institutions have presented partnerships with researchers from several countries such as the United States, France, Germany, Japan, Costa Rica and Spain. International collaboration with Brazil has been evidenced in several areas of science [7878 Gheno EM, Rosemberg DB, Souza DO, Calabró L. Zebrafish in Brazilian Science: Scientific Production, Impact, and Collaboration. Zebrafish. 2016;13:217-25.

79 Guimaraes VA, Ribeiro GM, Azevedo-Ferreira M. Mapping of the brazilian scientific publication on facility location. Pesquisa Operacional. 2018;38;307-30.
-8080 Hoppen NHF, Vanz SAD. Neurosciences in Brazil: a bibliometric study of main characteristics, collaboration and citations. Scientometrics. 2016;109:121-41.] and demonstrates that this collaboration is a trend of Brazilian researchers.

Species investigated

Among the 11 species with more studies about their peptides, 8 belong to the genus Bothrops, popularly known as jararacas. The species of this genus are distributed throughout all regions of Brazil and, due to this wide distribution, encounters with humans are common, making these snakes responsible for almost 90% of snakebites in the country [8181 Matos RR, Ignotti E. Incidência de acidentes ofídicos por gêneros de serpentes nos biomas brasileiros [Incidence of snakebites by snake genera in Brazilian biomes]. Cien Saude Cole. 2020;25:2837-46.]. The B. jararaca species has been studied from 1975 to the present day in terms of bradykinin-potentiating peptides [2020 Tominaga M, Stewart JM, Paiva TB, Paiva ACM. Synthesis and properties of new bradykinin potentiating peptides. Eur J Med Chem. 1975;18:130-3., 4141 Gilio JM, Portaro FC, Borella MI, Lameu C, Camargo AC, Alberto-Silva C. A bradykinin-potentiating peptide (BPP-10c) from Bothrops jararaca induces changes in seminiferous tubules. J Venom Anim Toxins Incl Trop Dis. 2012;19:28., 8282 Murayama N, Hayashi MAF, Ohi H, Ferreira LAF, Hermann VV, Saito H, et al. Cloning and sequence analysis of a Bothrops jararaca cDNA encoding a precursor of seven bradykinin-potentiating peptides and a C-type natriuretic peptide. Proc Natl Acad Sci. 1997;94:1189-93.

83 Perpetuo EA, Juliano L, Lebrun I. Biochemical and Pharmacological Aspects of Two Bradykinin-Potentiating Peptides Obtained from Tryptic Hydrolysis of Casein. J Protein Chem. 2003;22:601-6.

84 Nery AA, Trujillo CA, Lameu C, Konno K, Oliveira V, Camargo ACM, et al. A novel physiological property of snake bradykinin-potentiating peptides—Reversion of MK-801 inhibition of nicotinic acetylcholine receptors. Peptides. 2008;29:1708-15.

85 Campeiro JD, Neshich IP, Sant'Anna OA, Lopes R, Ianzer D, Assakura MT, et al. Identification of snake bradykinin-potentiating peptides (BPPs)-simile sequences in rat brain--Potential BPP-like precursor protein? Biochem Pharmacol. 2015;96:202-15.
-8686 Querobino SM, Ribeiro CAJ, Alberto-Silva C. Bradykinin-potentiating PEPTIDE-10C, an argininosuccinate synthetase activator, protects against H2O2 -induced oxidative stress in SH-SY5Y neuroblastoma cells. Peptides. 2018;103:90-7.]. These peptides are antihypertensive molecules that inhibit the degradation of a hypotensive peptide and the formation of a vasoconstrictor peptide [8787 Silveira P, Breno M, Martín del Río M, Mancera J. The distribution of vasotocin and mesotocin immunoreactivity in the brain of the snake, Bothrops jararaca. J Chem Neuroanat. 2002;24: 15-26.]. Other studies have evaluated antifungal peptides [3333 Gomes VM, Carvalho AO, Da Cunha M, Keller MN, Bloch C, Deolindo P, et al. Purification and characterization of a novel peptide with antifungal activity from Bothrops jararaca venom. Toxicon. 2005;45:817-27.], pituitary neuropeptides [8888 Lameu C, Pontieri V, Guerreiro J, Oliveira EF, Silva CA, Giglio JM, et al. Brain nitric oxide production by a proline-rich decapeptide from Bothrops jararaca venom improves baroreflex sensitivity of spontaneously hypertensive rats. Hypertension Research. 2010;33:1283-8.] and have discovered new hypotensive peptides in the snake's plasma [7373 Mesquita LS, Frias FT, Carmona E, Borgheresi RA. Differences in endothelin receptor types in the vasculature of Bothrops jararaca (Viperidae) and Oxyrhopus guibei (Colubridae) snakes. Comp Biochem Physiol C Toxicol Pharmacol. 2008;148:61-7.].

The antihypertensive activity of a proline-rich peptide (Bj-PRO-10c) isolated from the poison [8989 Benedetti G, Morais KLP, Guerreiro JR, Oliveira EF, Hoshida MS, Oliveira L, et al. Bothrops jararaca Peptide with Anti-Hypertensive Action Normalizes Endothelium Dysfunction Involved in Physiopathology of Preeclampsia. PLoS ONE. 2011;6:e3680.] has also been documented. This same peptide has been linked by Brazilian researchers to the normalization of endothelial dysfunction related to preeclampsia, which is a disease characterized by hypertension during pregnancy, that is, the peptide is useful as an antihypertensive in cases of preeclampsia and can be effective for new treatments against the disease [9090 Negraes PD, Lameu C, Hayashi MAF, Melo RL, Camargo ACM, Ulrich H. The snake venom peptide Bj-PRO-7a is a M1 muscarinic acetylcholine receptor agonist. Cytometry A. 2010;79:77-83.]. Still about B. jararaca peptides rich in proline, the properties of Bj-PRO 7a were also investigated by Brazilian researchers [9191 Turones LC, Cruz KR, Camargo-Silva G, Reis-Silva LL, Graziani D, Ferreira PM, et al. Behavioral effects of Bj-PRO-7a, a proline-rich oligopeptide from Bothrops jararaca venom. Braz J Med Biol Res. 2019;52:e8441.]. The peptides called Bj-PROs are recognized for being inhibitors of the angiotensin-converting enzyme and having pharmacological action, which resulted in the antihypertensive drug, Captopril [9292 Alberto-Silva C, Gilio JM, Portaro FCV, Querobino SM, Camargo ACM. Angiotensin-converting enzyme inhibitors of Bothrops jararaca snake venom affect the structure of mice seminiferous epithelium. J Venom Anim Toxins Incl Trop Dis. 2015;21:21-7.]. Brazilian researchers contributed to the knowledge about these peptides by also discovering that, in addition to lowering blood pressure, these peptides improve kidney function [77 Xavier CH, Miranda JRR, Yamaguchi J, Silveira KD, Teixeira MM, Chianca-Jr DA, et al. Bj-PRO-5a and Bj-PRO 10c Found at C-Type Natriuretic Peptide Precursor of Bothrops jararaca Change Renal Function of Hypertensive Rats. Int J Pept Res Ther. 2017;23:381-5.] and have anxiolytic and antidepressant effects in rats [9393 Alberto-Silva C, Franzin CS, Gilio JM, Bonfim RS, Querobino SM. Toxicological effects of bioactive peptide fractions obtained from Bothrops jararaca snake venom on the structure and function of mouse seminiferous epithelium. J Venom Anim Toxins Incl Trop Dis. 2020;26:e20200007.]. Studies with the species also evaluated the effects of bradykinin-potentiating peptides on the structure of the seminiferous tubules of rats [9393 Alberto-Silva C, Franzin CS, Gilio JM, Bonfim RS, Querobino SM. Toxicological effects of bioactive peptide fractions obtained from Bothrops jararaca snake venom on the structure and function of mouse seminiferous epithelium. J Venom Anim Toxins Incl Trop Dis. 2020;26:e20200007.-9494 Ferreira LAF, Henriques OB, Lebrun I, Batista MBC, Prezoto BC, Andreoni ASS, et al. A new bradykinin-potentiating peptide (peptide P) isolated from the venom of Bothrops jararacussu (Jararacuçu tapete, Urutu dourado). Toxicon. 1992;30:33-40.].

Another species of the Bothrops genus that has been studied by researchers in Brazil, is B. jararacussu, widely distributed in Brazil and neighboring countries, whose researches date from 1992 with a study about the bradykinin-potentiating peptides that are also found in the poison of this species [9595 Gebrim LC, Marcussi S, Menaldo DL, Menezes CSR, Nomizo A, Hamaguchi A, et al. Antitumor effects of snake venom chemically modified Lys49 phospholipase A2-like BthTX-I and a synthetic peptide derived from its C-terminal region. Biologicals. 2009;37:222-229.]. Over the years, new peptides of this class have been discovered [3535 Rioli V, Prezoto BC, Konno K, Melo RL, Klitzke CF, Ferro ES, et al. A novel bradykinin potentiating peptide isolated from Bothrops jararacussu venom using catallytically inactive oligopeptidase EP24.15. FEBS J. 2008; 275:2442-54.], with the evaluation of the antitumor activity [9393 Alberto-Silva C, Franzin CS, Gilio JM, Bonfim RS, Querobino SM. Toxicological effects of bioactive peptide fractions obtained from Bothrops jararaca snake venom on the structure and function of mouse seminiferous epithelium. J Venom Anim Toxins Incl Trop Dis. 2020;26:e20200007.] and antibacterial activities against multi-resistant bacteria [1717 Santos-Filho NA, Fernandes RS, Sgardiloi BF, Ramos MAS, Piccoli JP, Camargo IBC, et al. Antibacterial Activity of the Non-Cytotoxic Peptide (p-BthTX-I)2 and Its Serum Degradation Product against Multidrug-Resistant Bacteria. Molecules. 2017;22:1898.]. Studies with B. atrox, a snake that occurs in northern Brazil as well as other countries, have emerged more recently and bring information about the differences of the venom composition in the different stages of the animal's life [9797 Mello CP, Lima DB, Menezes RR, Bandeira ICJ, Tessarolo LD, Sampaio TL, et al. Evaluation of the antichagasic activity of batroxicidin, a cathelicidin-related antimicrobial peptide found in Bothrops atrox venom gland. Toxicon. 2017;130:56-62.]. In addition, the peptide functions of the species venom against mitochondrial swelling of the brain were considered, suggesting potential for neuroprotection [3737 Martins NM, Ferreira DAS, Carvalho Rodrigues MA, Cintra ACO, Santos NAG, Sampaio SV, et al. Low-molecular-mass peptides from the venom of the Amazonian viper Bothrops atrox protect against brain mitochondrial swelling in rat: Potential for neuroprotection. Toxicon. 2010;56:86-92.]. There was also potential against chagal disease of the batroxicidin peptide found in this species since the peptide induced cell death in the Trypanosoma cruzi parasite [9898 Sampaio SV, Cintra A, Costa T. Batroxin I, a New antitumor peptide isolated from Bothrops atrox snake venom. Toxicon. 2020;177:S23-S63.]. Another study characterized batroxin I as a peptide with antitumor potential [9999 Mariano-Oliveira A, Coelho ALJ, Terruggi CHB, Selistre-de-Araújo HS, Barja-Fidalgo C, De Freitas MS. Alternagin-C, a nonRGD-disintegrin, induces neutrophil migration via integrin signaling. Eur J Biochem. 2003;270:4799-808.].

The B. alternatus species had its peptides studied on chemotactic activities and inhibition of chemotaxis induced by a disintegrin [100100 Ramos OHP, Terruggi CHB, Ribeiro JU, Cominetti MR, Figueiredo CC, Bérard M, et al. Modulation of in vitro and in vivo angiogenesis by alternagin-C, a disintegrin-like protein from Bothrops alternatus snake venom and by a peptide derived from its sequence. Arch Biochem Biophys. 2007; 461:1-6.], a peptide that affects the proliferation of human vascular endothelial cells [101101 Van-de-Velde AC, Gay CC, Moritz MNO, Santos PK, Bustillo S, Rodríguez JP, et al. Purification of a fragment obtained by autolysis of a PIIIb-SVMP from Bothrops alternatus venom. Int J Biol Macromol. 2018;113:205-11.], in addition to the fragment purification of venom from this species [102102 Bourguignon S, Paes F, Calheiros E, Juliano M, Aguiar A, Melgarejo A, et al. Bothrops Moojeni Venom Peptides Containing Bradykinin Potentiating Peptides Sequences. Protein Pept Lett. 2001;8:21-6.]. For the species B. moojeni, a snake that also has a wide distribution in the Brazilian territory, new bradykinin-potentiating peptides were isolated [102102 Bourguignon S, Paes F, Calheiros E, Juliano M, Aguiar A, Melgarejo A, et al. Bothrops Moojeni Venom Peptides Containing Bradykinin Potentiating Peptides Sequences. Protein Pept Lett. 2001;8:21-6.], as well as, the renal toxicity of the poison was detected [6969 Barbosa PS, Havt A, Facó PE, Sousa TM, Bezerra ISAM, Fonteles MC, et al. Renal toxicity of Bothrops moojeni snake venom and its main myotoxins. Toxicon. 2002;40:1427-35.] and the anti-leishmania effect [104104 Amorim FG, Costa TR, Baiwir D, De Pauw E, Quinton L, Sampaio SV. Proteopeptidomic, Functional and Immunoreactivity Characterization of Bothrops moojeni Snake Venom: Influence of Snake Gender on Venom Composition. Toxins. 2018;10:177.]. For this species, the difference in the venom composition between males and females has been demonstrated [105105 Cintra ACO, Vieira CA, Giglio JR. Primary structure and biological activity of bradykinin potentiating peptides from Bothrops insularis snake venom. J Protein Chem. 1990;9:221-7.], as well as the identification of a new peptide derived from a metalloprotease with antimalarial action [4646 Martins GG, Holanda RHJ, Alfonso J, Garay AFG, Santos APZ, Lima AM, et al. Identification of a peptide derived from a Bothrops moojeni metalloprotease with in vitro inhibitory action on the Plasmodium falciparum purine nucleoside phosphorylase enzyme (PfPNP). Biochimie. 2019;162:97-106.], among other works.

The species B. insularis, on the other hand, draws attention due to its restricted distribution to an island in São Paulo and, despite this, to be present in many studies on peptides. For the species, there are studies that isolated several bradykinin-potentiating peptides even in the 90s [106106 Valente RH, Guimarães PR, Junqueira M, Neves-Ferreira AG, Soares MR, Chapeaurouge A, et al. Bothrops insularis venomics: a proteomic analysis supported by transcriptomic-generated sequence data. J Proteomics. 2009;72:241-55.], which identified peptides and proteins expressed by the snake venom gland [107107 Della-Casa MS, Junqueira-de-Azevedo I, Butera D, Clissa PB, Lopes DS, Serrano SMT, et al. Insularin, a disintegrin from Bothrops insularis venom: inhibition of platelet aggregation and endothelial cell adhesion by the native and recombinant GST-insularin proteins. Toxicon. 2011;57:125-33.], in addition to a study that isolated the insulin-disintegrin involved in physiological processes of endothelial cells [108108 Rodrigues VM, Marcussi S, Cambraia RS, de Araújo AL, Malta-Neto NR, Hamaguchi A, et al. Bactericidal and neurotoxic activities of two myotoxic phospholipases A2 from Bothrops neuwiedi pauloensis snake venom. Toxicon. 2004;44:305-14.]. The species B. neuwiedi has also been the subject of a study that isolated and characterized bradykinin-potentiating peptides [1616 Ferreira SH. Aspectos históricos da hipertensão [Historical aspects of hypertension]. HiperAtivo. 1998;5:230-232.], and others that characterized the snake's venom in terms of proteins and peptides [109109 Corrêa EA, Kayano AM, Diniz-Sousa R, Setúbal SS, Zanchi FB, Zuliani JP, et al. Isolation, structural and functional characterization of a new Lys49 phospholipase A 2 homologue from Bothrops neuwiedi urutu with bactericidal potential. Toxicon. 2016;115:13-21.-110110 Bello CA, Hermogenes ALN, Magalhaes A, Veiga SS, Gremski LH, Richardson M, et al. Isolation and biochemical characterization of a fibrinolytic proteinase from Bothrops leucurus (White-Tailed Jararaca) snake venom. Biochimie. 2006;88:189-200.]. Finally, in relation to this genus, the species B. leucurus has been investigated over the years as to the composition of its venom [111111 Magalhães A, Magalhães HP, Richardson M, Gontijo S, Ferreira RN, Almeida AP, et al. Purification and properties of a coagulant thrombin-like enzyme from the venom of Bothrops leucurus. Comp Biochem Physiol Part A Mol Integr Physiol. 2007;146:565-75.-112112 Gomes MSR, de Queiroz MR, Mamede CCN, Mendes MM, Hamaguchi A, Homsi-Brandeburgo MI, et al. Purification and functional characterization of a new metalloproteinase (BleucMP) from Bothrops leucurus snake venom. Comp Biochem Physiol C Toxicol Pharmacol. 2011;153:290-300.].

For another genus, attention is drawn to the species C. durissus, a snake widely distributed throughout Brazil, which occupies the second position among the most evaluated by snake peptide researchers in the country. Studies by Brazilian researchers investigating the composition of the venom of this species since 1993 have been found in the databases [6262 Oguiura N, Boni-Mitake M, Rádis-Baptista G. New view on crotamine, a small basic polypeptide myotoxin from South American rattlesnake venom. Toxicon. 2005;46:363-70.]. Among the publications, we highlight the studies with crotamine peptide, which causes spasms in the skeletal muscles and paralysis in the hind limbs in mice, in addition to antibacterial, hemolytic and antitumor activity [6363 Brigatte P, Faiad OJ, Ferreira Nocelli RC, Landgraf RG, Palma MS, Cury Y, et al. Walker 256 Tumor Growth Suppression by Crotoxin Involves Formyl Peptide Receptors and Lipoxin A4. Mediators Inflamm. 2016;2016:1-11., 6464 Mambelli-Lisboa NC, Sciani JM, Silva ARBP, Kerkis I. Co-Localization of Crotamine with Internal Membranes and Accentuated Accumulation in Tumor Cells. Molecules. 2018;23:968., 113113 Nunes ES, Souza MAA, Vaz AFM, Santana GMS, Gomes FS, Coelho LCBB, et al. Purification of a lectin with antibacterial activity from Bothrops leucurus snake venom. Comp Biochem Physiol B Biochem Mol Biol. 2011;159:57-63.

114 Ponce-Soto LA, Martins-de-Souza D, Marangoni S. Structural and pharmacological characterization of the crotamine isoforms III-4 (MYX4_CROCu) and III-7 (MYX7_CROCu) isolated from the Crotalus durissus cumanensis venom. Toxicon. 2010;55: 1443-52.
-115115 Oliveira KC, Spencer PJ, Ferreira-Jr RS, Nascimento N. New insights into the structural characteristics of irradiated crotamine. J Venom Anim Toxins Incl Trop Dis. 2015;21:1-10.]. Over the years, papers has been found with purification of crotoxin inhibitor which is the main component of snake venom [2727 Perales J, Villela C, Domont GB, Choumet V, Saliou B, Moussatché H, et al. Molecular structure and mechanism of action of the crotoxin inhibitor from Crotalus durissus terrificus serum. Eur J Biochem. 1995;227:19-26.], as well as the action mechanism and the structure of another component of the species venom, convulxin, which causes cardiovascular and respiratory disorders [116116 Falcao CB, Rádis-Baptista G. Crotamine and crotalicidin, membrane active peptides from Crotalus durissus terrificus rattlesnake venom, and their structurally-minimized fragments for applications in medicine and biotechnology. Peptides. 2019;126:170234.-117117 Francischetti IMB, Saliou B, Leduc MR, Carlini C, Hatmi M, Randon J, et al. COnvulxin, a potent platelet-aggregating protein from Crotalus durissus terrificus venom, specifically binds to platelets. Toxicon. 1997;35:1217-28.], about peptides involved in anti-inflammatory activity [118118 Murakami MT, Zela SP, Gava LM. Estrutura cristalina do ativador plaquetário convulxina, um tetrâmero cíclico alfa4beta4 ligado por dissulfeto do veneno de Crotalus durissus terrificus [Crystal structure of the convulxin platelet activator, a disulfide-linked alpha4beta4 cyclic tetramer from Crotalus durissus terrificus venom]. Comunicações de pesquisa bioquímicos e biofísicos. 2003;310:478-82.] as bradykinin-potentiating [119119 Nunes FP, Zychar BC, Della-Casa MS, Sampaio SC, Gonçalves LR, Cirillo MC. Crotoxin is responsible for the long-lasting anti-inflammatory effect of Crotalus durissus terrificus snake venom: involvement of formyl peptide receptors. Toxicon. 2010;55:1100-6.] and, more recently, new peptides found in the C. durissus venom with antimicrobial activity have been characterized [4747 Oliveira NGJ, Cardoso MH, Velikova N, Giersbers M, Wells JM, Rezende TMB, et al. Physicochemical-guided design of cathelicidin-derived peptides generates membrane active variants with therapeutic potential. Sci Rep. 2020;10:9127.].

In addition to these, the species L. muta and M. corallinus were also highlights among the most studied. As for L. muta, bradykinin-potentiating peptides were identified [120120 Lopes DM, Junior NE, Costa PP, Martins PL, Santos CF, Carvalho EDF, et al. A new structurally atypical bradykinin-potentiating peptide isolated from Crotalus durissus cascavella venom (South American rattlesnake). Toxicon. 2014;90:36-44.-121121 Soares MR, Oliveira-Carvalho AL, Wermelinger LS, Zingali RB, Ho PL, Junqueira-de-Azevedo IL, et al. Identification of novel bradykinin-potentiating peptides and C-type natriuretic peptide from Lachesis muta venom. Toxicon. 2005;46:31-8.], among many others. As for the species M. corallinus, attention was focused on natriuretic peptides, important in blood pressure homeostasis [122122 Pinheiro-Júnior EL, Boldrini-França J, Campos-Araújo LMP, Santos-Filho NA, Bendhack LM, Cilli EM, et al. LmrBPP9: A synthetic bradykinin-potentiating peptide from Lachesis muta rhombeata venom that inhibits the angiotensin-converting enzyme activity in vitro and reduces the blood pressure of hypertensive rats. Peptides. 2018;102:1-7.] and on strategies against snake poisoning [123123 Ho PL, Soares MB, Maack T, Gimenez I, Puorto G, Furtado MFD, et al. Cloning of an Unusual Natriuretic Peptide from the South American Coral Snake Micrurus corallinus. Eur J Biochem. 1997;250:144-9.-124124 Leão LI, Ho PL, Junqueira-de-Azevedo IL. Transcriptomic basis for an antiserum against Micrurus corallinus (Coral snake) venom. BMC Genomics. 2009;16:112.], among other studies that helped to understand other venom components of this species. Finally, it is interesting to note that, despite the many partnerships with foreign researchers, the attention of Brazilian researchers has been focused on species occurring in the national territory and in neighboring countries. Over the years, much has been discovered about the venom composition of snakes that occur in the country, especially about peptides.

Acknowledgments:

The authors would like to thank Dr. Cassia Cristina Fernandes Alves for her contribution to the structuring of the manuscript

  • Funding: This research was funded by Coordination for the Improvement of Higher Education Personnel (CAPES), National Council for Scientific and Technological Development (CNPq) grant number 477044/2013-1, Goiano Federal Institute, Brazilian Fund for Biodiversity (FUNBIO), Humanize Institute and Eurofins Foundation.

REFERENCES

  • 1
    Bernardes CP, Santos NAG, Sisti FM, Ferreira RS, Santos-Filho NA, Cintra ACO, et al. A synthetic snake-venom-based tripeptide (Glu-Val-Trp) protects PC12 cells from MPP+ toxicity by activating the NGF-signaling pathway. Peptides. 2018;104:24-34.
  • 2
    Almeida JR, Resende LM, Watanabe RK, Corassola VC, Huancahuire-Veja S, Caldeira CADS, et al. Snake venom peptides and low mass proteins: Molecular tools and therapeutic agentes. Curr Med Chem. 2017;24:3254-82.
  • 3
    Almeida JR, Mendes B, Lancelloti M, Marangoni S, Vale N, Passos O, et al. A novel synthetic peptide inspired on Lys49 phospholipase A 2 from Crotalus oreganus abyssus snake venom active against multidrug-resistant clinical isolates. Eur J Med Chem. 2018;149:248-56.
  • 4
    Vonk FJ, Jackson K, Doley R, Madaras F, Mirtschin PJ, Vidal N. Snake venom: From fieldwork to the clinic. BioEssays. 2011;33:269-79.
  • 5
    Remelli M, Brasili D, Guerrini R, Pontecchiani F, Potocki S, Rouwinska-Zyrek M, Watly J, et al. Zn(II) and Ni(II) complexes with poly-histidyl peptides derived from a snake venom. Inorganica Chim Acta. 2018;472:149-56.
  • 6
    Dal Mas C, Pinheiro DA, Campeiro JD, Mattei B, Oliveira V, Oliveira EB, et al. Biophysical and biological properties of small linear peptides derived from crotamine, a cationic antimicrobial/antitumoral toxin with cell penetrating and cargo delivery abilities. Biochim Biophys Acta Biomembr. 2017;1859:2340-9.
  • 7
    Xavier CH, Miranda JRR, Yamaguchi J, Silveira KD, Teixeira MM, Chianca-Jr DA, et al. Bj-PRO-5a and Bj-PRO 10c Found at C-Type Natriuretic Peptide Precursor of Bothrops jararaca Change Renal Function of Hypertensive Rats. Int J Pept Res Ther. 2017;23:381-5.
  • 8
    Chippaux JP, Williams V, White J. Snake venom variability: Methods of study, results and interpretation. Toxicon. 1991;29:1279-303.
  • 9
    Sanhajariya S, Duffull SB, Isbister GK. Pharmacokinetics of Snake Venom. Toxins. 2018;10:73.
  • 10
    Zelanis A. Abordagens sistêmicas em toxinologia: Perspectivas e implicações de metodologias ômicas no estudo de toxinas de venenos de serpentes. Estud Biol Ambiente Divers. 2012;34:143-7.
  • 11
    Oliveira AS, Fantinel AL, Artuzo FD, Oliveira L, Singer RB, Frota-Júnior MLC, et al. Applications of venom biodiversity in agriculture. EFB Bioeconomy Journal. 2021;100010.
  • 12
    Madella-Auricchio CR, Auricchio P, Soares ES. Reptile species composition in the Middle Gurguéia and comparison with inventories in the eastern Parnaíba River Basin, State of Piauí, Brazil. Pap Avulsos Zool. 2017;57:375-86.
  • 13
    Navega-Gonçalves MEC, Porto T. Conservação de serpentes nos biomas brasileiros [Snake conservation in Brazilian biomes]. Bioikos. 2016;30: 55-76.
  • 14
    Rocha e Silva M, Beraldo WT, Andrade SO. A new factor (Bradykinin) released from plasma globulin by snake venom and trypsin. Procedures of the First International Congress of Biochemistry. 1949;119.
  • 15
    Ferreira SH. A bradykinin-potentiating factor (BPF) present in the venom of Bothrops jararaca Br J Pharmacol. 1965;24:163-9.
  • 16
    Ferreira SH. Aspectos históricos da hipertensão [Historical aspects of hypertension]. HiperAtivo. 1998;5:230-232.
  • 17
    Santos-Filho NA, Fernandes RS, Sgardiloi BF, Ramos MAS, Piccoli JP, Camargo IBC, et al. Antibacterial Activity of the Non-Cytotoxic Peptide (p-BthTX-I)2 and Its Serum Degradation Product against Multidrug-Resistant Bacteria. Molecules. 2017;22:1898.
  • 18
    Maluf SEC, Dal Mas C, Oliveira EB, Melo PM, Carmona AK, Gazarini ML, et al. Inhibition of malaria parasite Plasmodium falciparum development by crotamine, a cell penetrating peptide from the snake venom. Peptides. 2016;78:11-6.
  • 19
    Sulca MA, Remuzgo C, Cardenas J, Kiyota S, Cheng E, Bemquerer MP, et al. Venom of the Peruvian snake Bothriopsis oligolepis: Detection of antibacterial activity and involvement of proteolytic enzymes and C-type lectins in growth inhibition of Staphylococcus aureus Toxicon. 2017;134: 30-40.
  • 20
    Tominaga M, Stewart JM, Paiva TB, Paiva ACM. Synthesis and properties of new bradykinin potentiating peptides. Eur J Med Chem. 1975;18:130-3.
  • 21
    Lavras AC, Fichman M, Hiraichi E, Boucault MA, Tobo T. Components of the renin-angiotensin system in the plasma of Bothrops jararaca Agents Actions. 1978;8:141-5.
  • 22
    Mandelbaum FR, Reichel AP, Assakura MT. Isolation and characterization of a proteolytic enzyme from the venom of the snake Bothrops jararaca (Jararaca). Toxicon. 1982;20:955-72.
  • 23
    Silva JN, Griffin PR, Aird SD. Comparative chromatography of Brazilian coral snake (Micrurus venoms). Comp Biochem Physiol B Biochem Mol Biol. 1991;100:117-26.
  • 24
    Sanchez EF, Diniz CR, Richardson M. The complete amino acid sequence of the haemorrhagic factor LHFII, a metalloproteinase isolated from the venom of the bushmaster snake (Lachesis muta muta). FEBS Letters. 1991;282: 178-82.
  • 25
    Fernandes PD, Guimarães JA Assreuy J. Comparative effects of two potentiating peptides (KPP and BPP9a) on kinin-induced rat paw edema. Agents Actions. 1991;32:182-7.
  • 26
    Jerusalinsky D, Cerveñansky C, Walz R, Bianchin M, Izquierdo I. A peptide muscarinic toxin from the Green Mamba venom shows agonist-like action in an inhibitory avoidance learning task. Eur J Pharmacol. 1993;240:103-5.
  • 27
    Perales J, Villela C, Domont GB, Choumet V, Saliou B, Moussatché H, et al. Molecular structure and mechanism of action of the crotoxin inhibitor from Crotalus durissus terrificus serum. Eur J Biochem. 1995;227:19-26.
  • 28
    Mancin AC, Soares AM, Andrião-Escarso SH, Faça VM, Greene LJ, Zuccolotto S, et al. The analgesic activity of crotamine, a neurotoxin from Crotalus durissus terrificus (South American rattlesnake) venom: A biochemical and pharmacological study. Toxicon. 1998;36:1927-37.
  • 29
    Oliveira JS, Silva ÁRBP, Soares MB, Stephano MA, Dias WO, Raw I, et al. Cloning and Characterization of an α-Neurotoxin-Type Protein Specific for the Coral Snake Micrurus corallinus Biochem Biophys Res Commu. 2000;267:887-91.
  • 30
    Oliveira UC, Assui A, Silva ÁRBP, Oliveira JS, Ho PL. Cloning and characterization of a basic phospholipase A2 homologue from Micrurus corallinus (Coral snake) venom gland. Toxicon. 2003;42: 249-55.
  • 31
    Ianzer D, Konno K, Marques-Porto R, Vieira Portaro FC, Stöcklin R, Martins de Camargo AC, et al. Identification of five new bradykinin potentiating peptides (BPPs) from Bothrops jararaca crude venom by using electrospray ionization tandem mass spectrometry after a two-step liquid chromatography. Peptides. 2004;25:1085-92.
  • 32
    Fernandez JH, Neshich G, Camargo AC. Using bradykinin-potentiating peptide structures to develop new antihypertensive drugs. Genet Mol Res. 2004;3:554-63.
  • 33
    Gomes VM, Carvalho AO, Da Cunha M, Keller MN, Bloch C, Deolindo P, et al. Purification and characterization of a novel peptide with antifungal activity from Bothrops jararaca venom. Toxicon. 2005;45:817-27.
  • 34
    Rizzi CT, Carvalho-de-Souza JL, Schiavon E, Cassola AC, Wanke E, Troncone LRP. Crotamine inhibits preferentially fast-twitching muscles but is inactive on sodium channels. Toxicon. 2007;50:553-62.
  • 35
    Rioli V, Prezoto BC, Konno K, Melo RL, Klitzke CF, Ferro ES, et al. A novel bradykinin potentiating peptide isolated from Bothrops jararacussu venom using catallytically inactive oligopeptidase EP24.15. FEBS J. 2008; 275:2442-54.
  • 36
    Cardoso R, Homsi-Brandeburgo MI, Rodrigues VM, Santos WB, Souza GLR, Prudencio CR, et al. Peptide mimicking antigenic and immunogenic epitope of neuwiedase from Bothrops neuwiedi snake venom. Toxicon. 2009; 53:254-61.
  • 37
    Martins NM, Ferreira DAS, Carvalho Rodrigues MA, Cintra ACO, Santos NAG, Sampaio SV, et al. Low-molecular-mass peptides from the venom of the Amazonian viper Bothrops atrox protect against brain mitochondrial swelling in rat: Potential for neuroprotection. Toxicon. 2010;56:86-92.
  • 38
    Martins-Santos MES, Resende RR, Pinto FCH, Soares AM, Marangoni S, Oliveira E, et al. Effect of a Pool of Peptides Isolated from Crotalus durissus terrificus (South American Rattlesnake) Venom on Glucose Levels of Mice Fed on a High-Fat Diet. Int J Pept Res Ther. 2011;17:225-230.
  • 39
    Silva SL, Almeida JR, Resende LM, Martis W, Henriques FAFA, Baldasso PA, et al. Isolation and characterization of a natriuretic peptide from Crotalus oreganus abyssus (grand canyon rattlesnake) and its effects on systemic blood pressure and nitrite levels. Int J Pept Res Ther. 2011;17:165-73.
  • 40
    Okubo BM, Silva ON, Migliolo L, Gomes DG, Porto WF, Batista CL, et al. Evaluation of an Antimicrobial L-Amino Acid Oxidase and Peptide Derivatives from Bothropoides mattogrosensis Pitviper Venom. PLoS ONE. 2012;7:e33639.
  • 41
    Gilio JM, Portaro FC, Borella MI, Lameu C, Camargo AC, Alberto-Silva C. A bradykinin-potentiating peptide (BPP-10c) from Bothrops jararaca induces changes in seminiferous tubules. J Venom Anim Toxins Incl Trop Dis. 2012;19:28.
  • 42
    Martins NM, Santos NA, Sartim MA, Cintra AC, Sampaio SV, Santos AC. A tripeptide isolated from Bothrops atrox venom has neuroprotective and neurotrophic effects on a cellular model of Parkinson's disease. Chem Biol Interact. 2015;235:10-6.
  • 43
    Dal Mas C, Moreira JT, Pinto S, Monte GG, Nering MB, Oliveira EB, et al. Anthelmintic effects of a cationic toxin from a South American rattlesnake venom. Toxicon. 2016;116:49-55.
  • 44
    Cavalcante C, Falcão C, Fontenelle R, Andreu D, Rádis-Baptista G. Anti-fungal activity of Ctn[15-34], the C-terminal peptide fragment of crotalicidin, a rattlesnake venom gland cathelicidin. J Antibiot. 2017;70:231-7.
  • 45
    Bandeira ICJ, Bandeira-Lima D, Mello CP, Pereira TP, Menezes RRPPB, Sampaio TL, et al. Antichagasic effect of crotalicidin, a cathelicidin-like vipericidin, found in Crotalus durissus terrificus rattlesnake's venom gland. Parasitology. 2018;145:1059-64.
  • 46
    Martins GG, Holanda RHJ, Alfonso J, Garay AFG, Santos APZ, Lima AM, et al. Identification of a peptide derived from a Bothrops moojeni metalloprotease with in vitro inhibitory action on the Plasmodium falciparum purine nucleoside phosphorylase enzyme (PfPNP). Biochimie. 2019;162:97-106.
  • 47
    Oliveira NGJ, Cardoso MH, Velikova N, Giersbers M, Wells JM, Rezende TMB, et al. Physicochemical-guided design of cathelicidin-derived peptides generates membrane active variants with therapeutic potential. Sci Rep. 2020;10:9127.
  • 48
    Fusco LS, Neto EB, Francisco AF, Alfonso J, Soares A, Pimenta DC, et al. Fast venomic analysis of Crotalus durissus terrificus from northeastern Argentina. Toxicon: X. 2020;100047.
  • 49
    Terra RMS, Pinto AFM, Guimarães JA, Fox JW. Proteomic profiling of snake venom metalloproteinases (SVMPs): Insightsinto venom induced pathology. Toxicon. 2009;54:836-44.
  • 50
    Viala VL, Hildebrand D, Fucase TM, Sciani JM, Prezotto-Neto JP, Riedner M, et al. Proteomic analysis of the rare Uracoan rattlesnake Crotalus vegrandis venom: Evidence of a broad arsenal of toxins. Toxicon. 2015;107:234-51.
  • 51
    Zorzetto R, Razzouk D, Dubugras MTB, Gerolin J, Schor N, Guimarães JA, et al. The scientific production in health and biological sciences of the top 20 Brazilian universities. Braz J Med Biol Res. 2006;39:1513-20.
  • 52
    Luchs A. Profile of Brazilian scientific production on A/H1N1 pandemic influenza. Cien Saúde Colet. 2012;17:1629-34.
  • 53
    Tarazona B, Vidal-Infer A, Alonso-Arroyo A. Bibliometric analysis of the scientific production in implantology (2009-2013). Clin Oral Implants Res. 2016;28:864-70.
  • 54
    Coutinho RX, Dávila ES, dos Santos WM, Rocha JBT, Souza DOG, Folmer V, et al. Brazilian scientific production in science education. Scientometrics. 2012;92:697-710.
  • 55
    Manzano-Agugliaro F, Alcayde A, Montoya FG, Zapata-Sierra A, Gil C. Scientific production of renewable energies worldwide: An overview. Renew Sustain Energy Rev. 2013;18:134-43.
  • 56
    Funchal-Witzel MDR, Castro LLC, Romano-Lieber NS, Narvai PC. Brazilian scientific production on pharmaceutical care from 1990 to 2009. Braz J Pharm Sci. 2011;47:409-20.
  • 57
    Franco M, Kalil J. The Butantan Institute: History and Future Perspectives. PLOS Negl Trop Dis. 2014;8:e2862.
  • 58
    Corrêa-Junior MC, Maria DA, Moura-da-Silva AM, Pizzocaro KF, Ruiz IR. Inhibition of melanoma cells tumorigenicity by the snake venom toxin jararhagin. Toxicon. 2002;40:739-48.
  • 59
    Zelanis A, Andrade-Silva D, Rocha MM, Furtado MF, Serrano SM, Junqueira-de-Azevedo IL, et al. A transcriptomic view of the proteome variability of newborn and adult Bothrops jararaca snake venoms. PLoS Negl Trop Dis. 2012; 6:e1554.
  • 60
    Menezes MC, Kitano ES, Bauer VC, Oliveira AK, Cararo-Lopes E, Nishiyama-Jr MY, et al. Early response of C2C12 myotubes to a sub-cytotoxic dose of hemorrhagic metalloproteinase HF3 from Bothrops jararaca venom. J Proteomics. 2019;198:163-76.
  • 61
    Giorgi R, Bernardi MM, Cury Y. Analgesic effect evoked by low molecular weight substances extracted from Crotalus durissus terrificus venom. Toxicon. 1993;31:1257-65.
  • 62
    Oguiura N, Boni-Mitake M, Rádis-Baptista G. New view on crotamine, a small basic polypeptide myotoxin from South American rattlesnake venom. Toxicon. 2005;46:363-70.
  • 63
    Brigatte P, Faiad OJ, Ferreira Nocelli RC, Landgraf RG, Palma MS, Cury Y, et al. Walker 256 Tumor Growth Suppression by Crotoxin Involves Formyl Peptide Receptors and Lipoxin A4. Mediators Inflamm. 2016;2016:1-11.
  • 64
    Mambelli-Lisboa NC, Sciani JM, Silva ARBP, Kerkis I. Co-Localization of Crotamine with Internal Membranes and Accentuated Accumulation in Tumor Cells. Molecules. 2018;23:968.
  • 65
    Mandelbaum FR, Assakura MT, Reichl AP. Characterization of two hemorrhagic factors isolated from the venom of Bothrops neuwiedi (Jararaca pintada). Toxicon. 1984;22:193-206.
  • 66
    Assakura MT, Reichl AP, Asperti MCA, Mandelbaum FR. Isolation of the major proteolytic enzyme from the venom of the snake Bothrops moojeni (Caissaca). Toxicon. 1985;23:691-706.
  • 67
    Castro VRO, Vernon LP. Hemolytic activity of thionin from Pyrularia pubera nuts and snake venom toxins of Naja naja species: Pyrulariathionin and snake venom cardiotoxin compete for the same membrane site. Toxicon. 1989;27:511-7.
  • 68
    Sanchez EF, Cordeiro MN, De-Oliveira EB, Juliano L, Prado ES, Diniz CR. Proteolytic specificity of two hemorrhagic factors, LHF-I and LHF-II, isolated from the venom of the bushmaster snake (Lachesis muta muta). Toxicon. 1995;33: 1061-9.
  • 69
    Barbosa PS, Havt A, Facó PE, Sousa TM, Bezerra ISAM, Fonteles MC, et al. Renal toxicity of Bothrops moojeni snake venom and its main myotoxins. Toxicon. 2002;40:1427-35.
  • 70
    Silva CA, Ianzer DA, Portaro FCV, Konno K, Faria M, Fernandes BL, et al. Characterization of urinary metabolites from four synthetic bradykinin potentiating peptides (BPPs) in mice. Toxicon. 2008;52: 501-7.
  • 71
    Querobino SM, Costa MS, Alberto-Silva C. Protective effects of distinct proline-rich oligopeptides from B. jararaca snake venom against oxidative stress-induced neurotoxicity. Toxicon. 2019;167:29-37.
  • 72
    Higuchi S, Murayama N, Saguchi K, Ohi H, Fujita Y, da Silva NJ, et al. A novel peptide from the ACEI/BPP-CNP precursor in the venom of Crotalus durissus collilineatus Comp Biochem Physiol C Toxicol Pharmacol. 2006;144:107-21.
  • 73
    Mesquita LS, Frias FT, Carmona E, Borgheresi RA. Differences in endothelin receptor types in the vasculature of Bothrops jararaca (Viperidae) and Oxyrhopus guibei (Colubridae) snakes. Comp Biochem Physiol C Toxicol Pharmacol. 2008;148:61-7.
  • 74
    Barreto SA, Chaguri LCAG, Prezoto BC, Lebrun I. Effects of three vasoactive peptides isolated from the plasma of the snake Bothrops jararaca Comp Biochem Physiol C Toxicol Pharmacol. 2009;149:552-8.
  • 75
    Torres-Bonilla KA, Andrade-Silva D, Serrano SMT, Hyslop S. Biochemical characterization of venom from Pseudoboa neuwiedii (Neuwied’s false boa; Xenodontinae; Pseudoboini). Comp Biochem Physiol C Toxicol Pharmacol. 2018;213:27-38.
  • 76
    Monteiro DA, Kalinin AL, Selistre-de-Araújo HS, Nogueira LAN, Beletti ME, Fernandes MN, et al. Cardioprotective effects of alternagin-C (ALT-C), a disintegrin-like protein from Rhinocerophis alternatus snake venom, on hypoxia-reoxygenation-induced injury in fish. Biochem Physiol C Toxicol Pharmacol. 2019;215:67-75.
  • 77
    Hilário CM, Grácio MCC. Scientific collaboration in Brazilian researches: a comparative study in the information science, mathematics and dentistry fields. Scientometrics, 2017;113:929-50.
  • 78
    Gheno EM, Rosemberg DB, Souza DO, Calabró L. Zebrafish in Brazilian Science: Scientific Production, Impact, and Collaboration. Zebrafish. 2016;13:217-25.
  • 79
    Guimaraes VA, Ribeiro GM, Azevedo-Ferreira M. Mapping of the brazilian scientific publication on facility location. Pesquisa Operacional. 2018;38;307-30.
  • 80
    Hoppen NHF, Vanz SAD. Neurosciences in Brazil: a bibliometric study of main characteristics, collaboration and citations. Scientometrics. 2016;109:121-41.
  • 81
    Matos RR, Ignotti E. Incidência de acidentes ofídicos por gêneros de serpentes nos biomas brasileiros [Incidence of snakebites by snake genera in Brazilian biomes]. Cien Saude Cole. 2020;25:2837-46.
  • 82
    Murayama N, Hayashi MAF, Ohi H, Ferreira LAF, Hermann VV, Saito H, et al. Cloning and sequence analysis of a Bothrops jararaca cDNA encoding a precursor of seven bradykinin-potentiating peptides and a C-type natriuretic peptide. Proc Natl Acad Sci. 1997;94:1189-93.
  • 83
    Perpetuo EA, Juliano L, Lebrun I. Biochemical and Pharmacological Aspects of Two Bradykinin-Potentiating Peptides Obtained from Tryptic Hydrolysis of Casein. J Protein Chem. 2003;22:601-6.
  • 84
    Nery AA, Trujillo CA, Lameu C, Konno K, Oliveira V, Camargo ACM, et al. A novel physiological property of snake bradykinin-potentiating peptides—Reversion of MK-801 inhibition of nicotinic acetylcholine receptors. Peptides. 2008;29:1708-15.
  • 85
    Campeiro JD, Neshich IP, Sant'Anna OA, Lopes R, Ianzer D, Assakura MT, et al. Identification of snake bradykinin-potentiating peptides (BPPs)-simile sequences in rat brain--Potential BPP-like precursor protein? Biochem Pharmacol. 2015;96:202-15.
  • 86
    Querobino SM, Ribeiro CAJ, Alberto-Silva C. Bradykinin-potentiating PEPTIDE-10C, an argininosuccinate synthetase activator, protects against H2O2 -induced oxidative stress in SH-SY5Y neuroblastoma cells. Peptides. 2018;103:90-7.
  • 87
    Silveira P, Breno M, Martín del Río M, Mancera J. The distribution of vasotocin and mesotocin immunoreactivity in the brain of the snake, Bothrops jararaca J Chem Neuroanat. 2002;24: 15-26.
  • 88
    Lameu C, Pontieri V, Guerreiro J, Oliveira EF, Silva CA, Giglio JM, et al. Brain nitric oxide production by a proline-rich decapeptide from Bothrops jararaca venom improves baroreflex sensitivity of spontaneously hypertensive rats. Hypertension Research. 2010;33:1283-8.
  • 89
    Benedetti G, Morais KLP, Guerreiro JR, Oliveira EF, Hoshida MS, Oliveira L, et al. Bothrops jararaca Peptide with Anti-Hypertensive Action Normalizes Endothelium Dysfunction Involved in Physiopathology of Preeclampsia. PLoS ONE. 2011;6:e3680.
  • 90
    Negraes PD, Lameu C, Hayashi MAF, Melo RL, Camargo ACM, Ulrich H. The snake venom peptide Bj-PRO-7a is a M1 muscarinic acetylcholine receptor agonist. Cytometry A. 2010;79:77-83.
  • 91
    Turones LC, Cruz KR, Camargo-Silva G, Reis-Silva LL, Graziani D, Ferreira PM, et al. Behavioral effects of Bj-PRO-7a, a proline-rich oligopeptide from Bothrops jararaca venom. Braz J Med Biol Res. 2019;52:e8441.
  • 92
    Alberto-Silva C, Gilio JM, Portaro FCV, Querobino SM, Camargo ACM. Angiotensin-converting enzyme inhibitors of Bothrops jararaca snake venom affect the structure of mice seminiferous epithelium. J Venom Anim Toxins Incl Trop Dis. 2015;21:21-7.
  • 93
    Alberto-Silva C, Franzin CS, Gilio JM, Bonfim RS, Querobino SM. Toxicological effects of bioactive peptide fractions obtained from Bothrops jararaca snake venom on the structure and function of mouse seminiferous epithelium. J Venom Anim Toxins Incl Trop Dis. 2020;26:e20200007.
  • 94
    Ferreira LAF, Henriques OB, Lebrun I, Batista MBC, Prezoto BC, Andreoni ASS, et al. A new bradykinin-potentiating peptide (peptide P) isolated from the venom of Bothrops jararacussu (Jararacuçu tapete, Urutu dourado). Toxicon. 1992;30:33-40.
  • 95
    Gebrim LC, Marcussi S, Menaldo DL, Menezes CSR, Nomizo A, Hamaguchi A, et al. Antitumor effects of snake venom chemically modified Lys49 phospholipase A2-like BthTX-I and a synthetic peptide derived from its C-terminal region. Biologicals. 2009;37:222-229.
  • 96
    Guércio RA, Shevchenko A, Shevchenko A, López-Lozano JL, Paba J, Sousa MV, et al. Ontogenetic variations in the venom proteome of the Amazonian snake Bothrops atrox Proteome Sci. 2006;4:11.
  • 97
    Mello CP, Lima DB, Menezes RR, Bandeira ICJ, Tessarolo LD, Sampaio TL, et al. Evaluation of the antichagasic activity of batroxicidin, a cathelicidin-related antimicrobial peptide found in Bothrops atrox venom gland. Toxicon. 2017;130:56-62.
  • 98
    Sampaio SV, Cintra A, Costa T. Batroxin I, a New antitumor peptide isolated from Bothrops atrox snake venom. Toxicon. 2020;177:S23-S63.
  • 99
    Mariano-Oliveira A, Coelho ALJ, Terruggi CHB, Selistre-de-Araújo HS, Barja-Fidalgo C, De Freitas MS. Alternagin-C, a nonRGD-disintegrin, induces neutrophil migration via integrin signaling. Eur J Biochem. 2003;270:4799-808.
  • 100
    Ramos OHP, Terruggi CHB, Ribeiro JU, Cominetti MR, Figueiredo CC, Bérard M, et al. Modulation of in vitro and in vivo angiogenesis by alternagin-C, a disintegrin-like protein from Bothrops alternatus snake venom and by a peptide derived from its sequence. Arch Biochem Biophys. 2007; 461:1-6.
  • 101
    Van-de-Velde AC, Gay CC, Moritz MNO, Santos PK, Bustillo S, Rodríguez JP, et al. Purification of a fragment obtained by autolysis of a PIIIb-SVMP from Bothrops alternatus venom. Int J Biol Macromol. 2018;113:205-11.
  • 102
    Bourguignon S, Paes F, Calheiros E, Juliano M, Aguiar A, Melgarejo A, et al. Bothrops Moojeni Venom Peptides Containing Bradykinin Potentiating Peptides Sequences. Protein Pept Lett. 2001;8:21-6.
  • 103
    Castilhos P, Pereira CG, Silva ALN, Napolitano DR, Oliveira F, Souza MA. Effects of Bothrops moojeni venom on Leishmania amazonensis promastigote forms. J Venom Anim Toxins Incl Trop Dis. 2011;17:150-8.
  • 104
    Amorim FG, Costa TR, Baiwir D, De Pauw E, Quinton L, Sampaio SV. Proteopeptidomic, Functional and Immunoreactivity Characterization of Bothrops moojeni Snake Venom: Influence of Snake Gender on Venom Composition. Toxins. 2018;10:177.
  • 105
    Cintra ACO, Vieira CA, Giglio JR. Primary structure and biological activity of bradykinin potentiating peptides from Bothrops insularis snake venom. J Protein Chem. 1990;9:221-7.
  • 106
    Valente RH, Guimarães PR, Junqueira M, Neves-Ferreira AG, Soares MR, Chapeaurouge A, et al. Bothrops insularis venomics: a proteomic analysis supported by transcriptomic-generated sequence data. J Proteomics. 2009;72:241-55.
  • 107
    Della-Casa MS, Junqueira-de-Azevedo I, Butera D, Clissa PB, Lopes DS, Serrano SMT, et al. Insularin, a disintegrin from Bothrops insularis venom: inhibition of platelet aggregation and endothelial cell adhesion by the native and recombinant GST-insularin proteins. Toxicon. 2011;57:125-33.
  • 108
    Rodrigues VM, Marcussi S, Cambraia RS, de Araújo AL, Malta-Neto NR, Hamaguchi A, et al. Bactericidal and neurotoxic activities of two myotoxic phospholipases A2 from Bothrops neuwiedi pauloensis snake venom. Toxicon. 2004;44:305-14.
  • 109
    Corrêa EA, Kayano AM, Diniz-Sousa R, Setúbal SS, Zanchi FB, Zuliani JP, et al. Isolation, structural and functional characterization of a new Lys49 phospholipase A 2 homologue from Bothrops neuwiedi urutu with bactericidal potential. Toxicon. 2016;115:13-21.
  • 110
    Bello CA, Hermogenes ALN, Magalhaes A, Veiga SS, Gremski LH, Richardson M, et al. Isolation and biochemical characterization of a fibrinolytic proteinase from Bothrops leucurus (White-Tailed Jararaca) snake venom. Biochimie. 2006;88:189-200.
  • 111
    Magalhães A, Magalhães HP, Richardson M, Gontijo S, Ferreira RN, Almeida AP, et al. Purification and properties of a coagulant thrombin-like enzyme from the venom of Bothrops leucurus Comp Biochem Physiol Part A Mol Integr Physiol. 2007;146:565-75.
  • 112
    Gomes MSR, de Queiroz MR, Mamede CCN, Mendes MM, Hamaguchi A, Homsi-Brandeburgo MI, et al. Purification and functional characterization of a new metalloproteinase (BleucMP) from Bothrops leucurus snake venom. Comp Biochem Physiol C Toxicol Pharmacol. 2011;153:290-300.
  • 113
    Nunes ES, Souza MAA, Vaz AFM, Santana GMS, Gomes FS, Coelho LCBB, et al. Purification of a lectin with antibacterial activity from Bothrops leucurus snake venom. Comp Biochem Physiol B Biochem Mol Biol. 2011;159:57-63.
  • 114
    Ponce-Soto LA, Martins-de-Souza D, Marangoni S. Structural and pharmacological characterization of the crotamine isoforms III-4 (MYX4_CROCu) and III-7 (MYX7_CROCu) isolated from the Crotalus durissus cumanensis venom. Toxicon. 2010;55: 1443-52.
  • 115
    Oliveira KC, Spencer PJ, Ferreira-Jr RS, Nascimento N. New insights into the structural characteristics of irradiated crotamine. J Venom Anim Toxins Incl Trop Dis. 2015;21:1-10.
  • 116
    Falcao CB, Rádis-Baptista G. Crotamine and crotalicidin, membrane active peptides from Crotalus durissus terrificus rattlesnake venom, and their structurally-minimized fragments for applications in medicine and biotechnology. Peptides. 2019;126:170234.
  • 117
    Francischetti IMB, Saliou B, Leduc MR, Carlini C, Hatmi M, Randon J, et al. COnvulxin, a potent platelet-aggregating protein from Crotalus durissus terrificus venom, specifically binds to platelets. Toxicon. 1997;35:1217-28.
  • 118
    Murakami MT, Zela SP, Gava LM. Estrutura cristalina do ativador plaquetário convulxina, um tetrâmero cíclico alfa4beta4 ligado por dissulfeto do veneno de Crotalus durissus terrificus [Crystal structure of the convulxin platelet activator, a disulfide-linked alpha4beta4 cyclic tetramer from Crotalus durissus terrificus venom]. Comunicações de pesquisa bioquímicos e biofísicos. 2003;310:478-82.
  • 119
    Nunes FP, Zychar BC, Della-Casa MS, Sampaio SC, Gonçalves LR, Cirillo MC. Crotoxin is responsible for the long-lasting anti-inflammatory effect of Crotalus durissus terrificus snake venom: involvement of formyl peptide receptors. Toxicon. 2010;55:1100-6.
  • 120
    Lopes DM, Junior NE, Costa PP, Martins PL, Santos CF, Carvalho EDF, et al. A new structurally atypical bradykinin-potentiating peptide isolated from Crotalus durissus cascavella venom (South American rattlesnake). Toxicon. 2014;90:36-44.
  • 121
    Soares MR, Oliveira-Carvalho AL, Wermelinger LS, Zingali RB, Ho PL, Junqueira-de-Azevedo IL, et al. Identification of novel bradykinin-potentiating peptides and C-type natriuretic peptide from Lachesis muta venom. Toxicon. 2005;46:31-8.
  • 122
    Pinheiro-Júnior EL, Boldrini-França J, Campos-Araújo LMP, Santos-Filho NA, Bendhack LM, Cilli EM, et al. LmrBPP9: A synthetic bradykinin-potentiating peptide from Lachesis muta rhombeata venom that inhibits the angiotensin-converting enzyme activity in vitro and reduces the blood pressure of hypertensive rats. Peptides. 2018;102:1-7.
  • 123
    Ho PL, Soares MB, Maack T, Gimenez I, Puorto G, Furtado MFD, et al. Cloning of an Unusual Natriuretic Peptide from the South American Coral Snake Micrurus corallinus Eur J Biochem. 1997;250:144-9.
  • 124
    Leão LI, Ho PL, Junqueira-de-Azevedo IL. Transcriptomic basis for an antiserum against Micrurus corallinus (Coral snake) venom. BMC Genomics. 2009;16:112.

Edited by

Editor-in-Chief: Paulo Vitor Farago
Associate Editor: Renata Marino Romano

Publication Dates

  • Publication in this collection
    27 June 2022
  • Date of issue
    2022

History

  • Received
    25 June 2021
  • Accepted
    22 Mar 2022
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