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Effects of butyric acid and arsenic on isolated pancreatic islets and liver mitochondria of male mouse.

Authors :
Ahangarpour, Akram
Oroojan, Ali Akbar
Rezaei, Mohsen
Khodayar, Mohammad Javad
Alboghobeish, Soheila
Zeinvand, Marzieh
Source :
Gastroenterology & Hepatology from Bed to Bench; Winter2017, Vol. 10 Issue 1, p44-53, 10p
Publication Year :
2017

Abstract

Aim: The aim of the present study was to evaluate the different doses of Butyric acid (BA) and Arsenic (As) in liver mitochondria oxidative stress and pancreatic islet insulin secretion of male mouse. Background: BA is found in many foods and As as a toxic metal is present in drinking water. They can induce oxidative stress in tissues. Methods: In this experimental study, Liver mitochondria were isolated by administration of the different centrifugation method and pancreatic islets were isolated by collagenase method. Mitochondria were incubated by BA (35, 75, 150, 300 µM) and As (20, 50, 100, 200 µM) as the islets were incubated by BA (250, 500, 1000, 1500 µM) and As (50, 100, 200 µM) for 1 hour. At the end of the experiment, mitochondrial viability and membrane potential, ROS, MDA, GSH and islets insulin secretion were measured by their specific methods. Results: BA and As administration increased mitochondrial levels of ROS, MDA and decreased GSH and pancreatic islet insulin secretion in a dose dependent manner (p<0.05). The doses of BA 75µM and As 100µM have been revealed the most mitochondria toxic concentrations. Also, the doses of 1000µM for BA and 100µM for As were considered as reducing concentrations for islets insulin secretion. Additionally, co administration of them intensified more these effects Conclusion: Alone or in combination administration of BA and As induced oxidative stress in liver mitochondria and decreased insulin secretion of pancreatic islets. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20082258
Volume :
10
Issue :
1
Database :
Complementary Index
Journal :
Gastroenterology & Hepatology from Bed to Bench
Publication Type :
Academic Journal
Accession number :
121733958