Abstract

Introduction: Dysregulated apoptosis is associated with a number of disease conditions. Traditionally, Calliandra portoricensis is used in the management of prostate enlargement. This study investigates the in vivo effect of potent methanol fraction of C. portoricensis (MFCP) on mitochondrial permeability transition (mPT) pore, an important pharmacological target in treatment of various diseases, and examines the toxicities associated with its oral administration.Methods: Forty-two male Wistar strain rats (70-80 g) were divided into 6 groups of 7 animals each. Each group was orally administered 25, 50, 100, 200, 400 mg/kg MFCP and the control group received distilled water for 21 and 30 days, respectively. mPT, assay for serum enzymes and hematological parameters were assessed spectrophotometrically while activation of caspases 3 and 9 was done by ELISA technique. Histological assessment of vital organs (liver, kidney, prostate) was carried out according to standard procedures.Results: There were no significant effects on mPT pore at all doses administered after 21 days of oral administration. However, after 30 days of administration, MFCP induced mPT pore opening at doses 100 and 200 mg/kg with induction folds of 2.6 and 3.3, respectively while there was no induction of mPT pore opening at lower doses of 25 mg/kg and 50 mg/kg. Furthermore, significant (P < 0.05) increases in serum enzymes (ALT, AST) were observed at all doses administered when compared with control after 30 days of oral administration. Cell counts (Hb, PCV, RBC, WBC) were adversely affected at the highest dose (200 mg/kg) compared with control and other treated groups (25, 50 and 100 mg/kg) after 30 days of administration. Similarly, activation of caspases 9 and 3 were observed in rat liver homogenate at high doses of the fraction while histological evaluation showed degeneration and distortion of organs at the highest dose.Conclusion: MFCP contains phytochemicals that elicit the opening of the pore and induction of mitochondrial-mediated apoptosis. This would be relevant in treatment of degenerative diseases that results from down-regulation of apoptosis. However, caution should be exercised in using high doses of the plant.

Highlights

  • Dysregulated apoptosis is associated with a number of disease conditions

  • Our preliminary data reveals that methanol fraction of C. portoricensis (MFCP) is potent with respect to induction of opening of the mitochondrial permeability transition (mPT) pore, enhancement of mitochondrial ATPase activity and activation of cytochrome C in vitro [16]

  • Effects of various doses of methanol fraction (MFCP) on rat liver mPT pore in the absence and presence of calcium (21 & 30 days) Mitochondria were isolated from control animals and mitochondrial swelling assay was carried out

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Summary

Introduction

Dysregulated apoptosis is associated with a number of disease conditions. Traditionally, Calliandra portoricensis is used in the management of prostate enlargement. This study investigates the in vivo effect of potent methanol fraction of C. portoricensis (MFCP) on mitochondrial permeability transition (mPT) pore, an important pharmacological target in treatment of various diseases, and examines the toxicities associated with its oral administration. Our preliminary data reveals that methanol fraction of C. portoricensis (MFCP) is potent with respect to induction of opening of the mPT pore, enhancement of mitochondrial ATPase activity and activation of cytochrome C in vitro [16]. Owing to the relevance of bioavailability of the compound of interest at the target site and to determine the safety dose regimen for the potent methanol fraction, in vivo assessment of the efficacy of the potent MFCP in induction of mPT pore opening, activation of caspases and the determination of its toxic effects in normal rat were investigated

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