ABSTRACT Various extracts obtained from the red alga Plocamium brasiliense (Greville Howe & Taylor), including a fraction containing crude 5-chloro-1-(E)-chlorovinyl-2,4-dibromo-1,5-dimethylcyclohexane (1) and another containing a mixture of halogenated monoterpenes (F), as well as atomaric acid meroditerpene (2) isolated from brown alga Stypopodium zonale (J. V. Lamouroux) Papenfuss, were evaluated for their activity against Trypanosoma cruzi. The cytotoxic and trypanosomicidal effects of these extracts were evaluated in Vero cells and clinically relevant forms of T. cruzi (amastigotes and trypomastigotes). All extracts from P. brasiliense presented low cytotoxicity and moderate trypanosomicidal effects, except for the hydroalcoholic extract. The crude 1 and F fractions had enhanced trypanocidal activity but showed low selectivity. Moreover, atomaric acid (2) was identified as a hit, demonstrating a potent trypanocidal effect reaching an IC50 <10 µM against two different DTU (Yand high selectivity index (<10). These results identify marine natural products as promising candidates against Chagas disease.

Resumen Los dolabellanos son diterpenos con actividad antiviral, la mayor parte de los estudios se han realizado con compuestos aislados de algas pardas del genero Dictyota. Los corales blandos son también una importante fuente de dolabellanos, pero el potencial antiviral de estos ha sido muy poco estudiado. Se llevó a cabo el estudio químico de los dolabellanos presentes en los octocorales Eunicea laciniata y Eunicea asperula, recolectados en Santa Marta, Caribe colombiano. Los dolabellanos 1-6 fueron aislados del octocoral E. laciniata mientras que en E. asperula se encontraron los compuestos 2, 4 y 5. La elucidaci6n estructural se llev6 a cabo mediante RMN, espectrometría de masas, rotaci6n 6ptica y comparaci6n con reportes previos. El análisis por CG-EM evidenci6 que la dolabellatrienona (2) se puede transformar en los compuestos 4 y 5 como producto del almacenamiento prolongado, no obstante, tales compuestos también estuvieron presentes en los extractos de los organismos estudiados. El compuesto 6 inhibi6 la replicaci6n del VHS-1 (73,7% de inhibición en células infectadas a una concentraci6n de 50 µM) sin efecto citot6xico (CC50 = 959), mostrando una citotoxicidad similar al Aciclovir®, un control positivo, por lo cual es un candidato para la realizaci6n de estudios adicionales sobre el potencial antiviral de los dolabellanos.

Abstract Dolabellane diterpenes have considerable antiviral activity, but most studies have been focused towards compounds isolated from Dictyota brown algae. Although soft corals are also a significant source of these diterpenes, their antiviral potential has not been studied in detail. With the aim of assessing the biological activity of marine sources, we evaluated the dolabellane content in the soft corals Eunicea laciniata and E. asperula collected in Santa Marta, Colombian Caribbean. Dolabellanes 1-6 were isolated from E. laciniata while compounds 2, 4 and 5 were isolated from E. asperula. All compounds were identified by NMR, GC-EIMS, optical rotation and comparison with previously reported dolabellanes. GC-EIMS analyses showed that dolabellatrienone (2) transforms into compounds 4 and 5 as oxidation products upon prolonged storage; however, those compounds were also naturally present in the extract of the studied organisms. Pure dolabellanes were tested in vitro in antiviral assays against HSV-1. Compound 6 inhibited virus replication in infected cells (73.7% of inhibition at 50 µM) without cytotoxic effect (CC50 = 95 9), showing similar activity to the positive control Acyclovir®. Thus, compound 6 is an interesting candidate for further studies of dolabellanes as antivirals.

Resumo Os dolabellanos são diterpenos que têm mostrado atividade antiviral, os estudos neste campo estão centrados nos compostos isolados de algas do gênero Dictyota. Os octocorais também são uma fonte importante de dolabellanos, mas não tem sido estudados. Foirealizado o estudo químico dos octocorais Eunicea laciniata e Eunicea asperula, coletados em Santa Marta, Caribe Colombiano. O estudo químico dos dois organismos permitiu o isolamento dos dolabellanos 1-6 de E. laciniata, enquanto que para E. aspérula foram identificados os compostos 2, 4 e 5. A elucidação estrutural foi realizada mediante RMN, espectrometria de massas, rotação óptica e comparação com os dados da literatura. A análise por GC-MS evidenciou que a dolabelatrienona (2) pode gerar os compostos 4 e 5 como produto de degradação, a partir de um armazenamento prolongado. No entanto, os compostos também estavam presentes nos extratos dos organismos estudados. O composto 6 mostrou uma citotoxicidade similar ao Aciclovir®, um controle positivo, numa porcentagem de inibição da replicação do HVS-1 (73,7% de inibição em células infectadas na concentração de 50 µM) sem efeito citotóxico (CC50 = 959), o quetorna esse composto um candidato para o desenvolvimento de antivirais.

Background Snakebite is considered a neglected tropical disease by the World Health Organization. In Brazil, about 70% of the envenomation cases are caused by Bothrops snakes. Its venom may provoke hemorrhage, pain, necrosis, hemolysis, renal or cardiac failure and even death in victims. Since commercial antivenom does not efficiently neutralize the local toxic effects of venoms, natural products have been tested in order to provide alternative or complementary treatment to serum therapy. Therefore, the present study aimed to evaluate the ability of the seaweed Plocamium brasiliense and its active derivatives to neutralize hemorrhagic, edematogenic, hemolytic, coagulant and proteolytic activities of B. jararaca venom. Methods Specimens of P. brasiliense were collected in Rio de Janeiro state, Brazil, dried and submitted to oil extraction using four solvents of increasing polarities, n-hexane (HEX), dichloromethane (DCM), ethyl acetate (ETA) and hydroalcoholic solution (HYD). The solvents were evaporated, yielding HEX, DCM, ETA and HYD extracts. Further, all extracts were dissolved in dimethylsulfoxide. In addition, two monoterpenes (8-bromo-3,4,7-trichloro-3,7-dimethyl-1E, 5E-octadiene and 1,8-dibromo-3,4,7-trichloro-3,7-dimethyl-1E, 5E-octadiene) and a cholesterol fraction were isolated from the extract of P. brasiliense prepared in hexane. Algal samples were incubated for 30 minutes with B. jararaca venom, and then tested for lethality; hemorrhagic, edematogenic, hemolytic, coagulant and proteolytic effects. Results Most of the algal extracts inhibited the toxic effects with different potencies. The DCM extract was the most effective, since it inhibited all types of toxic activity. On the other hand, the HYD extract failed to inhibit any effect. Moreover, the isolated products inhibited proteolysis and protected mice from hemorrhage in 30% of the cases, whereas 8-bromo-3,4,7-trichloro-3,7-dimethyl-1E, 5E-octadiene inhibited 100% and 20% of the hemorrhagic and proteolytic activities, respectively. None of the algal products were toxic to mice. Conclusion Seaweeds may be a promising source of inhibitors against toxic effects caused by B. jararacaenvenomation, which may contribute to antivenom treatment.

The crude extract of the marine brown alga Dictyota guineensis was analyzed by high-resolution gas chromatography-mass spectrometry (HRGC-MS). Five diterpenes were identified: dictyol E (the most abundant diterpene), dictyotadiol, dictyoxide, isopachydictyol A and pachydictyol A, all diterpenes from the chemical group I, i.e., mainly prenylated derivatives of known sesquiterpene skeletons that result from a first cyclization of geranyl-geraniol between positions 1 and 10. These diterpenes are known for their activity against bacteria, fungi and other activities. The results characterize D. guineensis as a species that yields exclusively diterpenes from group I, with low oxidation and low structural complexity. On Brazilian coasts, only D. mertensii provides exclusively prenylated guaiane diterpenes. Although D. guineensis presents alternate branches and fixing by rhizoidal branches, it is easily distinguishable from D. mertensii by the much narrower stem, short stature and flabelliform habit of the former species. On the other hand, both species have been characterized as producers of diterpenes of group I, in particular, prenylated guaiane. However, D. guineensis has a majority dictyol E in the lipophilic extract, while D. mertensii produces more complex prenylated guaianes, like dictyol H.

The effect of a Brazilian algae extract and also a mixture of two secodolastane diterpenes (linearol/isolinearol) that were isolated from the marine brown alga Canistrocarpus cervicornis were evaluated against biological activities of Lachesis muta snake venom. In vitro assays showed that the crude extract and the diterpenes were able to inhibit the clotting and proteolytic activity induced by L. muta crude venom, but not the hemolytic activity. However, only the diterpenes inhibited the hemolysis caused by a purified phospholipase A2 previously isolated from L. muta venom, denoted LM-PLA2-I. Interestingly, the crude algal extract and the diterpenes were able to protect mice from hemorrhage induced by L. muta venom. Thus, we may conclude that marine algae are rich and powerful sources of molecules that may be used against L. muta accidents in order to improve treatment of envenomation by this snake.

Dictyotaceae are a rich source of secondary metabolites, especially terpenes. These natural products have been studied for their bioactivity for human and for their ecological role in nature. The present work highlights de diversity of the Dictyotaceae terpenes, emphasizing their bioactivities and the biogeography of their sources. The sesquiterpenes are found in Padina, Dictyopteris and Taonia. Although Dictyopteris and Padina can be found in all oceans, Taonia has a more restricted distribution. Diterpenes of mixed origin have been reported in Lobophora, Taonia and Stypopodium. Stypopodium is a typically tropical and warm temperate genus. Diterpenes with the spatane and seco-spatanes skeletons are known from Spatoglossum, Stoechospermum and Rugulopteryx. Spatoglossum is distributed over all the tropical marine world. Stoechospermum is known to occur in the Indian Ocean and Rugulopteryx is distributed mainly in Asia and on the Pacific Coast of Australia. The genus Dictyota contains diterpenes as the major metabolite and are present in all oceans, reaching even the cold temperate regions of northern and southern hemispheres. The terpenoids from Dictyotaceae exhibit bioactivities such as inhibition of herbivores and antifungal, cytotoxic, antibiotic, anti-inflammatory, insecticidal and antiviral activities.

Diversos organismos bênticos possuem defesas químicas que ajudam a diminuir a predação. Embora sua eficácia seja comprovada, muitos de seus efeitos são ainda desconhecidos. Múltiplas funções dos metabolitos secundários foram evidenciadas em algumas esponjas e isso pode representar uma vantagem adaptativa, considerando o alto valor energético gasto pelas espécies para produzí-los. O objetivo desse trabalho foi investigar as propriedades defensivas de extratos da esponja Hymeniacidon heliophila contra predadores tropicais: paguros (Calcinus tibicens), ouriços-do-mar (Lytechinus variegatus) e peixes generalistas. Extratos em n-hexano, acetato de etila e acetona/metanol foram usados nos ensaios e todos foram eficientes na redução do consumo por C. tibicen; extratos em n-hexano reduziram o consumo por L. variegatus; e extratos de média polaridade reduziram o consumo por peixes. A variação na ação ou as funções ecológicas múltiplas dos extratos indicam que diferentes tipos de substâncias podem ser associadas ao sistema defensivo produzido por Hymeniacidon heliophila.

Various benthic organisms have chemical defenses which reduce their predators' consumption. Although their efficiency may be noticed in many organisms, many of their effects are not well- known yet. Multiple ecological roles of secondary metabolites are shown in some sponges, which may represent an adaptative advantage considering the high amount of energy used to produce these chemical compounds. The goal of this work was to investigate the defensive property of the extracts from the sponge Hymeniacidon heliophila against the tropical predators: hermit crabs (Calcinus tibicens), sea urchins (Lytechinus variegatus) and generalist fishes. Extracts obtained with n-hexane, ethyl acetate and acetone/methanol were used in assays and all of them were effective in reducing the consumption by C. tibicens; n-hexane extract reduced the consumption by L. variegatus; and medium polarity extracts reduced fish consumption. Either the variation in action or the multiple ecological roles of the extracts indicates that different types of compounds can be associated to the defensive system produced by H. heliophila.

Este artigo demonstra a química defensiva anti-herbivoria da macroalga parda marinha Canistrocarpus cervicornis. Em sua concentração natural, o extrato bruto em diclorometano (DCE) inibiu significativamente o consumo alimentar do ouriço-do-mar Lytechinus variegatus. Deste extrato em DCE foi isolado o metabólito majoritário identificado como o diterpeno (4R,7R,14S)-4α,7α-diacetoxi-14-hidroxidolasta-1(15),8-dieno. Esses resultados comprovam que diterpenos da classe dolastano podem compor o sistema defensivo anti-herbivoria de C. cervircornis e, supostamente, o de outras algas pardas capazes de produzi-los, uma vez que são composto típicos encontrados em esqueletos de Dyctiotas em todo o mundo. Este é o primeiro estudo demonstrando a ação anti-herbivoria desta classe de metabolitos (diterpenos dolastanos) em macroalgas marinhas. Tais informações ampliam o conhecimento sobre o papel desses metabolitos especiais em C. cervicornis e de espécies de Dyctiotae.

This paper reports on the defensive chemical properties of the marine tropical brown seaweed Canistrocarpus cervicornis against herbivory. A natural concentration of dichloromethane crude extract (DCE) obtained from this seaweed significantly inhibited feeding by the sea urchin Lytechinus variegatus. The major metabolite isolated from this active DCE extract was identified as the (4R,7R,14S)-4α,7α-diacetoxy-14-hydroxydolast-1(15),8-diene that strongly inhibited feeding by the same sea urchin. This result suggests that the dolastane diterpenes class may constitute the defensive system of C. cervicornis against herbivory, and probably also of that of other brown seaweeds endowed with a biosynthetic pathway capable of producing compounds of the dolastane-type, a typical skeleton found in Dyctioteae species worldwide. This is the first report showing this compound-type (dolastane diterpenes) as a chemical defense against herbivory in marine seaweeds. This study constitutes an additional report broadening the known spectrum of action and roles of secondary metabolites of the C. cervicornis and Dyctioteae species.

Os extratos brutos de espécimes da alga parda D. menstrualis, conhecida por produzir diterpenos como principais metabólitos secundários, foram analisados quanto ao modo de armazenamento antes da extração e tipo de solvente utilizado na obtenção do extrato bruto. Os solventes utilizados foram uma mistura diclorometano:metanol (2:1) e acetona. Os espécimes de D. menstrualis foram submetidos a três formas de armazenamento, denominados fresco, seco e congelado. Não foram observadas diferenças qualitativas nas amostras obtidas de quaisquer dos extratos brutos na análise por CG/EM, sendo compostas pelos diterpenos pachydictyol A (I), 6-hidroxi-dichotoma-3,14-dieno-1,17-dial (II), 6-hidroxi-2,7-cicloxenia-3,14-dieno-1,17-dial (III) e 6-acetoxi-dichotoma-3,14-dieno-1,17-dial (IV). Os resultados indicaram que a extração mais eficaz para os componentes de média polaridade de D. menstrualis foi obtida com o uso de acetona, que promoveu extração mais seletiva, mesmo apresentando menor rendimento em massa. Quanto à forma de armazenamento das algas, foi constatado que as metodologias não diferiram significativamente entre si, apesar da tendência de algas congeladas fornecerem o menor rendimento no total de diterpenos. Portanto, nos trabalhos envolvendo análises químicas de extratos brutos de macroalgas marinhas, a escolha do solvente de extração deve ser considerada como fator importante na varredura de substância bioativas.

Crude extracts from specimens of the brown seaweed Dictyota menstrualis, known to produce diterpenes as their major secondary metabolites, were analyzed according to storage procedures before extraction, and the solvent types used to obtain the crude extracts. The specimens of D. menstrualis were submitted to three types of storage procedures, such as wet, dry, and frozen and were extracted with a mixture of dichloromethane:methanol (2:1) and acetone. Qualitative differences were not observed by GC/MS analyses of all crude extracts containing mainly the diterpenes pachydictyol A (I), 6-hydroxy-dichotoma-3,14-diene-1,17-dial (II), 6-hydroxy-2,7-cycloxenia-3,14-diene-1,17-dial (III), and 6-acetoxy-dichotoma-3,14-diene-1,17-dial (IV). The most efficient and selective extraction of the compounds with intermediate polarity produced by D. menstrualis was obtained using acetone, but with less mass production. In general, the storage procedures produced very similar results, but the frozen samples furnished low amount of total diterpenes. According to these results on chemical analysis of crude extracts of seaweeds, the choice of solvent to extraction should be considered as important aspect to better screening bioactive compounds.

Os radicais livres e outros derivados ativos do oxigênio são inevitavelmente co-produzidos em algumas reações biológicas e exercem papel fisiológico importante. No entanto, essas espécies reativas têm sido descritas como fatores que participam diretamente dos mecanismos fisiopatológicos relacionados com a continuidade e as complicações de diversos estados patológicos como a aterosclerose, a diabetes, o câncer, a artrite reumatóide, entre outros. Dessa forma, a terapia antioxidante preveniria o desenvolvimento e a progressão dessas complicações. As algas marinhas representam uma importante fonte de substâncias antioxidantes naturais, uma vez que têm sistemas de defesas antioxidantes bem desenvolvidos. O presente trabalho é uma compilação das pesquisas realizadas sobre a atividade antioxidante de produtos naturais marinhos e extratos de algas marinhas bentônicas.

Free radicals and other reactive species of oxygen are co-produced in some biological reactions and they play important physiological role, and nevertheless they are reported as factors that take straight part in the pathophysiologic mechanism associated with continuity and complications of the several pathological process such as arteriosclerosis, diabetes mellitus, cancer, and arthritis, among others. In this way, the antioxidant therapy should prevent the development and progress of these complications. Seaweeds can be valuable source of natural antioxidant compounds since they have a well-developed antioxidant defense system. The present work is a compilation of the antioxidant activities of marine natural products and benthonic marine seaweeds crude extracts researches.

Os espécimes da macroalga parda Dictyota mertensii coletados em dois diferentes locais no litoral brasileiro e distantes entre si, Búzios (Rio de Janeiro) e Fernando de Noronha (PE), foram avaliados quanto à atuação de seus extratos como defesa química contra o caranguejo Pachygrapsus transversus, e o ouriço do mar Lytechinus variegatus. O extrato dos espécimes de D. mertensii de Búzios inibiu o consumo por ambos P. transversus e L. variegatus. O fracionamento dos extratos dos espécimes de D. mertensii de Búzios e F. de Noronha avaliados em ensaios complementares revelaram uma fração ativa contendo distintos metabolitos secundários defensivos. Diterpenos do tipo guaiano prenilado foram as substâncias majoritárias em ambas as frações, mas dictyol H e epoxipachydictyol A foram os mais abundantes em Búzios e F. de Noronha, respectivamente, seguidos por componentes minoritários. Nossos resultados mostram uma produção diferencial de metabolitos secundários em duas populações distintas e distantes de D. mertensii no litoral brasileiro e sugerem que as defesas químicas desta macroalga marinha não são uma característica qualitativa absoluta desta espécie e pode representar uma especialização ecológica eficaz para prevenir a herbivoria.

Crude extracts of the brown seaweed Dictyota mertensii (Martius) Kützing collected at two distant and different places on the Brazilian coast, Búzios (Rio de Janeiro) and Fernando de Noronha (PE), were evaluated for defensive chemistry against the crab Pachygrapsus transversus, and the sea urchin Lytechinus variegatus. The extract from Búzios specimens of D. mertensii significantly inhibited the consumption by both P. transversus and L. varigetaus. Fractionation of the extracts of specimens of D. mertensii from Búzios and F. de Noronha followed by complementary assays revealed one active fraction from each location, which contained distinct defensive secondary metabolites. In each active fractions prenylated guaiane diterpenes were the major compounds. Dictyol H and epoxypachydictyol A were the most abundant compounds in Búzios and F. de Noronha, respectively, followed by minor components. Our results show a differential production of secondary metabolites in the two distant and different populations of D. mertensii along the Brazilian coast. This suggests that defensive chemicals from this seaweed are not qualitatively absolute characteristics of the species, but may represent an ecological specialization to successfully prevent herbivory.

The present work is a revision on the ecological significance of the production of sesquiterpenes by the marine algae of the genus Laurencia (Ceramiales, Rhodophyta).