Progesterone and Cilostazol Protect mice pancreatic islets from oxidative stress induced by hydrogen peroxide

Authors

  • akram ahangarpour Dept. of Physiology, Diabetes Research Center and Physiology Research Center, Faculty of Medical Sciences, Ahvaz Jundishapur University of Medical Sciences, Ahvaz;
  • Ali Khodadadi Associate Professor. Cellular and Molecular Research Center (CMRC), Dept. of Immunology Science, Ahvaz Jundishapur University of Medical Sciences, Faculty of Medicine, Ahvaz, Iran.
  • Hamid Heidari Dept. of Physiology, Faculty of Medical Sciences, Ahvaz Jundishapur University of Medical Sciences, Ahvaz; Iran
  • Mahmoud Hashemitabar Associate Professor. Cellular and Molecular Research Center (CMRC), Dept. of Anatomical Science, Ahvaz Jundishapur University of Medical Sciences, Faculty of Medicine, Ahvaz, Iran.
  • Seyyed Ali Mard Physiology Research Center (PRC), Research institute for infectious diseases of digestive system and Dept. of Physiology, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
Abstract:

Abstract Reactive oxygen species and oxidative stress impair β-cell function and reduce insulin secretion. It has been shown that progesterone and cilostazol possess antioxidant properties. The present study was aimed to investigate in vitro pretreatment effect of progesterone and cilostazol on insulin secretion as well as their protective effects against hydrogen peroxide-induced oxidative stress in pancreatic isolated islets from mouse. Pancreatic islets were isolated from 84 male NMRI mice (25–30g) by collagenase digestion method and pretreated for 48h with cilostazol (10 μM), progesterone (0.5 µM) and glibenclamide (10 μM) in culture medium. Then islets were exposed to hydrogen peroxide (H2O2. 500 μM) for 2h. Next, culture mediums containing glucose concentration of 2.8 mM or 16.7 mM were added to them and incubated in this status for 1h. At the end, the rate of insulin out¬put from islets, lipid peroxidation and antioxidant enzymes activities in islet tissues were assayed. Exposure of islets to H2O2, resulted in a significant decrease in insulin secretion, superoxide dismutase and catalase activities (P

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Journal title

volume 13  issue 3

pages  937- 944

publication date 2014-07-01

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