MODULATION OF MITOCHONDRIAL MEDIATED APOPTOSIS BY SOLVENT FRACTIONS OF THE FRUIT EXTRACTS OF SARCOCEPHALUS LATIFOLIUS (SMITH) BRUCE

Joan Uchechukwu Imah-Harry; Olufunso Olabode  Olorunsogo

doi:10.22270/ujpr.v9i5.1205

Joan Uchechukwu Imah-Harry Department of Natural Sciences, Faculty of Pure and Applied Sciences, Precious Cornerstone University, Ibadan, Nigeria.
Olufunso Olabode Olorunsogo Laboratories for Biomembrane Research and Biotechnology Department of Biochemistry, College of Medicine, University of Ibadan, Nigeria.

10.22270/ujpr.v9i5.1205

Keywords:

Apoptosis, cancer, MOMP, mPT pore, Sarcocephalus latifolius

Abstract

Aim and Objective: However, this claim has not been scientifically substantiated. In this study, we investigated the inductive effect of the crude methanol extract (CMESL) and a chloroform subfraction (sCFSL) of Sarcocephalus latifolius fruits on mPT, in vivo.

Methods: Thirty-five male wistar rats (90±10 g) were acclimatized, divided into seven groups, and treated with 1% DMSO (control) and 25, 50, and 100 mg/kgbw of each of the fractions for thirty days. Rats were sacrificed and liver mitochondria were isolated by differential centrifugation. The MOMP, DNA fragmentation, p53, Bax and BCl-2 protein expressions, Cytochrome C release, and caspase – 3 and -9 activities were assayed in liver tissue by standard methods.

Results: CMESL and sCFSL induced mPT pore. The sCFSL induced MOMP maximally at 100 mg/kgbw, inhibited LPO (78%), enhanced mitochondrial ATPase activity (27.96±0.04 µmole/mg Protein/min) than CMESL (17.58± 0.03 µmole/mg Protein/min) at the same dose. Similarly, sCFSL caused DNA fragmentation; (77.33%), enhanced caspases -3 and -9 activation; increased p53 and Bax expression levels, increased Cytochrome C release, and downregulated BCl-2 protein expression, compared to CMESL.

Conclusion: These findings showed that sCFSL contains bioactive agents that can induce mitochondrial-mediated apoptosis, and therefore a potential target to be explored in the management of tumors and cancer.