Gliclazide and Crassocephalum rubens leaf extract inhibit glucose-induced mitochondrial permeability transition pore (MPTP) opening in isolated pancreas mitochondria of Wistar rats
سال انتشار: 1401
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 171
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شناسه ملی سند علمی:
JR_HERM-12-1_007
تاریخ نمایه سازی: 14 آذر 1402
چکیده مقاله:
Introduction: Mitochondrial permeability transition pore (MPTP) has been implicated in a wide variety of diseases such as cancer, neurodegenerative diseases, and diabetes. Crassocephalum rubens is a leafy vegetable consumed in different parts of Africa for the management of symptoms of diabetes mellitus, inflammation, malaria, and blood pressure. The present study evaluated the modulatory effects of aqueous leaf extract of C. rubens (ACR) and gliclazide on MPTP in the pancreas of Wistar albino rats in vitro.
Methods: Pancreatic mitochondria were isolated from experimental animals using standard protocols. Furthermore, MPTP was induced using various concentrations (۱۵, ۲۲.۵, ۳۰, and ۳۷.۵ mmol/L) of glucose and CaCl۲ (۳ μM). Alterations in MPTP and ameliorative potential of different concentrations of ACR (۸, ۲۴, ۴۰, ۵۶ μg/mL) and gliclazide (۰.۰۵۴ mg/mL) were monitored spectrophotometrically via changes in absorbance at ۵۴۰ nm for ۱۲ minutes, under sodium succinate energized condition.
Results: It was observed that ۳۰ mmol/L, ۳۷.۵ mmol/L D-glucose, and Ca۲+ significantly induced MPTP opening by ۰.۶۳۵, ۵.۱۰, and ۹.۹۵ folds, respectively, an effect that was reversed by gliclazide and ACR, in a none-dose dependent manner. In addition, ACR at ۵۶ μg/mL in conjunction with Ca۲+ opened the MPTP.
Conclusion: Data from this study suggest that gliclazide and ACR, especially at the lower concentrations, possess significant inhibitory effects against MPTP opening in the pancreas of male Wistar albino rats and, therefore, could be useful in protecting beta-cell death usually associated with diabetes mellitus, as well as other conditions in which MPTP opening is implicated.
کلیدواژه ها:
نویسندگان
Tajudeen Olabisi Obafemi
Department of Biochemistry, Afe Babalola University, PMB ۵۴۵۴ Ado-Ekiti, Nigeria
Blessing Ariyo Afolabi
Department of Biochemistry, Bowen University, PMB ۲۸۴, Iwo Nigeria
John Adeolu Falode
Department of Biochemistry, Federal University, Oye-Ekiti, Nigeria
Jerius Nkwnda Ejeje
Department of Biochemistry, Afe Babalola University, PMB ۵۴۵۴ Ado-Ekiti, Nigeria- Department of Biochemistry, Alex Ekwueme Federal University Ndufu Alike, P.O. Box ۱۰۱۰, Abakaliki, Nigeria