Electrical Properties of Isolated Cardiomyocytes in a Rat Model of Thiamine Deficiency

Abstracts

In modern society, thiamine deficiency (TD) remains an important medical condition linked to altered cardiac function. There have been contradictory reports about the impact of TD on heart physiology, especially in the context of cardiac excitability. In order to address this particular question, we used a TD rat model and patch-clamp technique to investigate the electrical properties of isolated cardiomyocytes from epicardium and endocardium. Neither cell type showed substantial differences on the action potential waveform and transient outward potassium current. Based on our results we can conclude that TD does not induce major electrical remodeling in isolated cardiac myocytes in either endocardium or epicardium cells.

Myocytes, Cardiac; Electric Stimulation; Thiamine Deficiency/ physiopathology; Action Potentials; Rats, Heart Failure

Na sociedade moderna, a deficiência de tiamina (DT) ainda é uma condição médica importante ligada à função cardíaca alterada. Há relatos contraditórios sobre o impacto da DT sobre a fisiologia do coração, especialmente no contexto da excitabilidade cardíaca. A fim de resolver essa questão em particular, nós utilizamos de um modelo de DT para investigar as propriedades elétricas de cardiomiócitos isolados das diferentes sub-regiões do miocárdio de ratos, epicárdio e endocárdio, por meio da técnica de “patch clamp”. Nenhum dos dois tipos de célula estudados apresentou diferenças significativas na morfologia do potencial de ação e corrente transitória rápida de saída de potássio. Com base em nossos resultados, podemos concluir que a DT não induz grande remodelamento elétrico em miócitos cardíacos isolados tanto nas células do endocárdio quanto nas do epicárdio.

Miócitos Cardíacos; Estimulação Elétrica; Deficiência de Tiamina/fisiopatologia; Potenciais de Ação; Ratos; Insuficiência Cardíaca

Introduction

Thiamine is a pivotal cofactor involved in distinct biochemical reactions. Its deprivation causes significant changes in physiology, especially in neurons and cardiac tissue¹. In the industrialized world, thiamine deficiency (TD) is particularly related to chronic alcohol consumption and administration of loop diuretics, such as furosemide¹. In both cases, some degree of heart remodeling is reported, such as high-output heart failure, the most common clinical manifestation of TD². In some cases, patients with TD may develop heart failure in association with cardiac electrical remodeling^2,3. Based on previous data from the literature and using animal models, our group and others have determined electrical remodeling of cardiomyocytes. However, there are conflicting results in the literature¹. In the present study, we determined whether TD leads to electrical remodeling of isolated myocytes from the endocardium (ENDO) and epicardium (EPI) of rats.

Methods

Experimental group

Male Wistar rats (250 g) were fed a control (containing thiamine) or a thiamine-free diet for 35 days as previously described by our group^4-6.

Cell isolation

ENDO and EPI cells of the left ventricle from age-matched control and TD rats were enzymatically dissociated as previously reported⁴.

Electrophysiological recordings

All records were obtained using methods and solutions as previously described⁵. Cells were maintained at a holding potential of -80mV. Action potentials (APs) were elicited by short pulses (3-5 ms) of 1nA current at 1 Hz frequency for 3 minutes. During K current records, cells were perfused with a modified Tyrode’s solution, replacing NaCl by N-metyl-D-glucamine (NMDG) (to abolish sodium current), and 100µM CdCl₂ (to block L-type calcium current). A junction potential of -20mV was measured and should be applied to every tested potential.

Statistical analysis

All results are expressed as mean ± standard error of the mean. For statistical analysis, we used One-way anova followed by Tukey’s post-hoc test. P < 0.05 was set as significant level.

Results

In the present study we evaluated the electrical properties of isolated myocytes from ENDO and EPI cells. Our results showed that control myocyte have longer action potential duration (APD) in ENDO cells when compared to EPI cells (Figure 1). This phenomenon is connected to larger outward potassium current in EPI when compared to ENDO cells (Figure 2), corroborating previous data from the literature. To our surprise, TD had minor impact on electrical properties of isolated cardiomyocytes. When compared the repolarization time (RT) at 90% of EPI CTR to EPI TD, it was 26.33 ± 1.56 ms, n = 26 vs. 30.35 ± 2.49 ms, n = 22, respectively. ENDO cells showed similar results. For instance, RT at 90% was 38.93 ± 2.96ms, n = 18 vs. 46.40 ± 6.11 ms, n = 20 for CTR vs. TD cells (Figure 1). In line with these results, peak outward and inward potassium current was similar, when comparing EPI CT to EPI TD. For example at +80 mV it was (A/F) 23.01 ± 1.77, n = 18 and 20.62 ± 1.50, n = 15, respectively. Similar profile was observed for ENDO cells (Figure 2). Finally, in line with previous results, TD myocytes showed smaller capacitance when compared to CTR cells (data not shown).

Figure 1
Action potentials in isolated cardiac myocytes. Top panels show representative recordings for (A) epicardium (EPI) cells (left) and (B) Endocardium (ENDO) cells (right), considering control (CT) (green line) and thiamine-deficient (TD) (blue line) groups. Bottom panels show average time required for the action potential repolarization to occur at 10%, 50% and 90% of the repolarization in control (green bars) and TD (blue bars) groups for EPI- CT (n = 26), EPI-DT (n = 22) (left) and ENDO-CT (n = 18), ENDO-TD (n = 20) (right).

Figure 2
Whole-cell potassium current. Currents were elicited upon stimulation steps ranging from -140 to +80mV (for 4s) from a holding potential of -70 mV in steps of 20 mV, every 15s. Top (CTR) and middle (TD) panels show representative recordings for (A) epicardium (EPI) and (B) endocardium (ENDO) cells. Insets represent the initial 500 ms of recordings. Bottom panels represent the current x voltage for maximum potassium current. Green and blue squares represent CTR and TD groups, for EPI (A) and ENDO (B) cells.

Discussion

In previous studies, using a rat model, our group showed that TD is able to induce cardiomyocyte contractility dysfunction⁷. Such changes were attributed to altered calcium handling, with reduced sarcoplasmatic reticulum calcium content⁸. Additionally, an increased production of reactive oxygen species (ROS) was observed, which may have contributed to the reduced heart mass observed in this model⁴. Together, these results are able to explain the reduced heart and myocyte function during TD.

In the context of electrical alteration, it is more difficult to draw a more conclusive idea. There have been many reports in the literature showing distinct alterations in the electrocardiogram of humans and animals during TD, including tachycardia, ST elevation and depression, altered T wave morphology with prolonged QT interval, accompanied by A-V block and QRS prolongation^2,9. In the context of animal models, it seems that cardiomyocytes from young rats are more prone to develop electrical disturbances than adult rats (the latter were used in the present study)¹.

However, it is intriguing that TD is not able to induce robust electrical remodeling in cardiomyocytes, especially in the context of increased ROS production⁴. It is well know that ROS is able reduce outward potassium current in myocytes, due to reduced expression of Kv_4.3, which is responsible for the transient outward potassium current¹⁰. Thus, it is possible to speculate that there are endogenous systems and/or aging factors that modulate the electrical remodeling of myocytes in the setting of TD.

Conclusion

Thiamine deficiency leads to minor changes in the electrical properties of isolated cardiac myocytes in both endocardium and epicardium cells. This study was supported by FAPEMIG, CNPq and CAPES.

• Sources of Funding
  This study was funded by CNPq, Capes e FAPEMIG.
• Study Association
  This study is not associated with any thesis or dissertation work.

References

• ¹
  Roman-Campos D, Cruz JS. Current aspects of thiamine deficiency on heart function. Life Sci.2014;98(1):1-5.
• ²
  Kawano H, Koide Y, Toda G, Yano K. ST-segment elevation of electrocardiogram in a patient with Shoshin beriberi. Intern Med.2005;44(6):578-85.
• ³
  Loma-Osorio P, Penafiel P, Doltra A, Sionis A, Bosch X. Shoshin beriberi mimicking a high-risk non-ST-segment elevation acute coronary syndrome with cardiogenic shock: when the arteries are not guilty. J Emerg Med.2011;41(4):e73-7.
• ⁴
  Gioda CR, de Oliveira Barreto T, Primola-Gomes TN, de Lima DC, Campos PP, Capettini L dos S, et al. Cardiac oxidative stress is involved in heart failure induced by thiamine deprivation in rats. Am J Physiol Heart Circ Physiol.2010;298(6):H2039-45.
• ⁵
  Roman-Campos D, Campos AC, Gioda CR, Campos PP, Medeiros MA, Cruz JS. Cardiac structural changes and electrical remodeling in a thiamine-deficiency model in rats. Life Sci.2009;84(23-24):817-24.
• ⁶
  Oliveira FA, Galan DT, Ribeiro AM, Santos Cruz J. Thiamine deficiency during pregnancy leads to cerebellar neuronal death in rat offspring: role of voltage-dependent K+ channels. Brain Res.2007;1134(1):79-86.
• ⁷
  Gioda CR, Roman-Campos D, Carneiro-Junior MA, da Silva KA, de Souza MO, Mendes LJ, et al. Impaired cellular contractile function in thiamine-deficient rat cardiomyocytes. Eur J Heart Fail. 2009;11(12):1126-8.
• ⁸
  Oliveira FA, Guatimosim S, Castro CH, Galan DT, Lauton-Santos S, Ribeiro AM, et al. Abolition of reperfusion-induced arrhythmias in hearts from thiamine-deficient rats. Am J Physiol Heart Circ Physiol.2007;293(1):H394-401.
• ⁹
  Rapuzzi G, Rindi G. Inluence of increasing heart rate on the alterations of the cardiac ventricular fibre-cells action potentials induced by thiamine deficiency. Q J Exp Physiol Cogn Med Sci.1967;52(3):277-84.
• ¹⁰
  Zhou C, Ziegler C, Birder LA, Stewart AF, Levitan ES. Angiotensin II and stretch activate NADPH oxidase to destabilize cardiac Kv4.3 channel mRNA. Circ Res.2006;98(8):1040-7.

Publication Dates

• Publication in this collection
  Mar 2015

History

• Received
  10 Oct 2014
• Reviewed
  24 Dec 2014
• Accepted
  24 Dec 2014