In vitro chronotropic effects of Erythrina senegalensis DC (Fabaceae) aqueous extract on mouse heart slice and pluripotent stem cell-derived cardiomyocytes

• Published in: Journal of ethnopharmacology 2015-05, Vol.165, p.163-172
• Main Authors: Nembo, Erastus Nembu, Atsamo, Albert Donatien, Nguelefack, Télesphore Benoît, Kamanyi, Albert, Hescheler, Jürgen, Nguemo, Filomain
• Format: Article
• Language: English
• Subjects: Animals; Cardiomyocytes; Chronotropy; Electrophysiologic Techniques, Cardiac; Erythrina - chemistry; Erythrina senegalensis; Heart - drug effects; Heart Rate - drug effects; Heart slice; Humans; In Vitro Techniques; Mice; Microelectrode arrays; Microelectrodes; Myocardial Contraction - drug effects; Myocytes, Cardiac - drug effects; Patch-clamp technique; Plant Bark - chemistry; Plant Extracts - pharmacology; Pluripotent Stem Cells - drug effects; Stem cells
• ISSN: 0378-8741; 1872-7573
• DOI: 10.1016/j.jep.2015.02.002

Erythrina senegalensis DC (Fabaceae) bark is commonly used in sub-Saharan traditional medicine for the treatment of many diseases including gastrointestinal disorders and cardiovascular diseases. In this study, we investigated the effect of the aqueous extract of the stem bark of Erythrina senegalensis on the contractile properties of mouse ventricular slices and human induced pluripotent stem (hiPS) cell-derived cardiomyocytes. We also investigated the cytotoxic effect of the extract on mouse embryonic stem (ES) cells differentiating into cardiomyocytes (CMs). We used well-established electrophysiological technologies to assess the effect of Erythrina senegalensis aqueous extract (ESAE) on the beating activity of mouse ventricular slices, mouse ES and hiPS cell-derived CMs. To study the cytotoxic effect of our extract, differentiating mouse ES cells were exposed to different concentrations of ESAE. EB morphology was assessed by microscopy at different stages of differentiation whereas cell viability was measured by flow cytometry, fluorometry and immunocytochemistry. The electrical activity of CMs and heart slices were respectively captured by the patch clamp technique and microelectrode array (MEA) method following ESAE acute exposure. Our findings revealed that ESAE exhibits a biphasic chronotropic activity on mouse ventricular slices with an initial low dose (0.001 and 0.01µg/mL) decrease in beating activity followed by a corresponding significant increase in chronotropic activity at higher doses above 10µg/mL. The muscarinic receptor blocker, atropine abolished the negative chronotropic activity of ESAE, while propranolol successfully blocked its positive chronotropic activity. ESAE showed a significant dose-dependent positive chronotropic activity on hiPS cell-derived CMs. Also, though not significantly, ESAE decreased cell viability and increased total caspase-3/7 activity of mouse ES cells in a concentration-dependent manner. Erythrina senegalensis aqueous extract exhibits a biphasic chronotropic effect on mouse heart and a positive chronotropic activity on hiPS cell-derived CMs, suggesting a possible mechanism through muscarinic and β-adrenergic receptor pathways. Also, ESAE is not cytotoxic on mouse ES cells at concentrations up to 100µg/mL. [Display omitted]