Sub-Chronic Effects of Pausinystalia yohimbe Methanol Extract on Cardiac and Inflammatory Biomarkers in Male Wistar Rats
Imafidon Joseph Omogiade *
Department of Medical Laboratory Science, Igbinedion University Okada, Nigeria.
Aghatise Kevin Erhamwonyi
Department of Medical Laboratory Science, Igbinedion University Okada, Nigeria.
Omogiade Christabe C.A.
Department of Medical Laboratory Science, Igbinedion University Okada, Nigeria.
Ekoyata Charles
Department of Medical Laboratory Science, Igbinedion University Okada, Nigeria.
Samuel Obuele Idibagen
Department of Medical Laboratory Science, Igbinedion University Okada, Nigeria.
*Author to whom correspondence should be addressed.
Abstract
Introduction: In sub-Saharan Africa, herbal aphrodisiacs are frequently used to improve sexual performance. Because of its bioactive alkaloid yohimbine, an α-adrenergic receptor antagonist that is known to alter sympathetic activity and vascular tone, Pausinystalia yohimbe (Burantashi) is one of the most well-liked. Despite its widespread usage, little is known about its systemic biochemical safety, especially with regard to indicators for cardiac and inflammatory harm.
Aim and Objectives: Using sildenafil citrate as a pharmacological comparator, this study assessed the sub-chronic effects of P. yohimbe methanol extract on cardiac troponin-I and high-sensitivity C-reactive protein (hs-CRP) levels in male Wistar rats.
Materials and Methods: Five groups (n = 5) of twenty-five adult male Wistar rats weighing 150–180 g were given sildenafil (5 mg/kg), P. yohimbe extract at 50, 100, and 200 mg/kg, and control (distilled water 5 mL/kg). For 28 days, the treatments were given orally. ELISA kits were used to measure serum CRP and troponin-I in accordance with manufacturer guidelines. The Student's t-test (SPSS v24; p < 0.05) was used to examine the data, which were presented as mean ± SE.
Results: Troponin-I stayed constant (0.34 ± 0.07 vs. 0.24 ± 0.02 ng/mL; p > 0.05), while sildenafil markedly increased CRP (2.74 ± 0.11 mg/L) in comparison to control (2.30 ± 0.07 mg/L; p = 0.011). Troponin-I and CRP did not significantly change when P. yohimbe was administered at 50 and 100 mg/kg. At 200 mg/kg, however, there was no change in troponin-I (0.22 ± 0.37 ng/mL; p = 0.667), while CRP increased considerably (2.54 ± 0.08 mg/L vs 2.30 ± 0.07 mg/L; p = 0.049).
Conclusion: While high-dose exposure (200 mg/kg) causes a modest systemic inflammatory response without causing cardiac damage, low-to-moderate dosages (≤100 mg/kg) of methanolic P. yohimbe are biochemically safe. These results outline a first biochemical safety margin for the use of P. yohimbe.
Keywords: Pausinystalia yohimbe, C-reactive protein, troponin-I, inflammation, cardiotoxicity, Wistar rat, ELISA