• Title of article

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

  • Author/Authors

    Ahangarpour, Akram Department of Physiology - Health Research Institute - Diabetes Research Center - Ahvaz Jundishapur University of Medical Sciences, Iran , Oroojan, Ali Akbar Department of Physiology - Student Research Committee - Ahvaz Jundishapur University of Medical Science, Iran , Rezaei, Mohsen Department of Toxicology - Faculty of Medical Sciences - Tarbiat Modares University, Tehran, Iran , Khodayar, Mohammad Javad Department of Pharmacology and Toxicology - School of Pharmacy - Jundishapur University of Medical Sciences, Ahvaz, Iran , Alboghobeish, Soheila Department of Pharmacology - School of Pharmacy - Student Research Committee - Ahvaz Jundishapur University of Medical Sciences, Iran , Zeinvand, Marzieh Department of Toxicology - School of Pharmacy - Student Research Committee - Ahvaz Jundishapur University of Medical Sciences, Iran

  • Pages
    10
  • From page
    44
  • To page
    53
  • Abstract
    Aim: The aim of present study was to evaluate the different doses of Butyric acid (BA) and Arsenic (As) on mouse liver mitochondria oxidative stress and pancreatic islets insulin secretion. Background: BA is found in many foods and As is a toxic metal in drinking water. They can induce oxidative stress in some tissue. Materials and Methods: In this experimental study, Liver mitochondria were isolated by administration of different centrifugation method and pancreatic islets of mice were isolated by a collagenase method. Mitochondria by BA (35, 75, 150, 300 μM) and As (20, 50, 100, 200 μM) and the islets were incubated by BA (250, 500, 1000, 1500 μM) and As (0, 50, 100, 200 μM) for 1 hour. At the end of 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 exact mitochondria toxic concentrations were 75 ?M for BA and 100 ?M for As. Also, the doses of 1000 μM for BA and 100 μM for As were consider as reducing concentrations for islets insulin secretion. Additionally, coadministration of these doses of BA and As revealed an additive effect on their own tissues variables. Conclusion: Alone or in combination administration of BA and As induced oxidative stress in liver mitochondria and decreased insulin secretion of pancreatic islets.
  • Keywords
    Butyric acid , Arsenic , Liver mitochondria , Islet , Mouse
  • Journal title
    Gastroenterology and Hepatology From Bed to Bench
  • Serial Year
    2017
  • Record number

    2516722