Antioxidant and antiapoptotic effects of erdosteine in a rat model of ovarian ischemia-reperfusion injury

Authors

  • A Tuba Kocaman Yildiz Technical University, Biochemistry Division, Department of Bioengineering, Faculty of Chemical and Metallurgical Engineering, Istanbul, Turkey
  • Ahmet Cagatay Cicek University of Trakya, Faculty of Medicine, Department of Histology and Embryology, 22030, Balkan Campus, Edirne, Turkey
  • Mustafa Cemek Yildiz Technical University, Biochemistry Division, Department of Bioengineering, Faculty of Chemical and Metallurgical Engineering, Istanbul, Turkey
  • Selim Demirtas University of Trakya, Faculty of Medicine, Department of Histology and Embryology, 22030, Balkan Campus, Edirne, Turkey
  • Turan Karaca University of Trakya, Faculty of Medicine, Department of Histology and Embryology, 22030, Balkan Campus, Edirne, Turkey
  • Vedat Ugurel University of Trakya, Faculty of Medicine, Department of Obstetrics and Gynecology, 22030, Balkan Campus, Edirne, Turkey
Abstract:

Objective(s): To evaluate the protective effect of erdosteine, an antiapoptotic and antioxidant agent, on torsion–detorsion evoked histopathological changes in experimental ovarian ischemia-reperfusion (IR) injury. Materials and Methods: Eighteen female Wistar albino rats were used in control, IR, and IR+Edosteine (IR-E) groups, (n=6 in each). The IR-E group received the erdosteine for seven days before the induction of torsion/retorsion, (10 mg/kg/days). The IR and IR-E groups were exposed to right unilateral adnexal torsion for 3 hr. Three hours later, re-laparotomy was performed, and the right ovaries were surgically excised. Oxidant and antioxidants levels were determined in serum. The ovarian tissue samples were received and fixed with 10% neutral buffered formalin. The sections were stained with H&E, anti-PCNA, and TUNEL. Results: The IR group were showed severe acute inflammation, polynuclear leukocytes and macrophages, stromal oedema and haemorrhage. Treatment with erdosteine in rats significantly retained degenerative changes in the ovaryPCNA (+) cell numbers were significantly decreased in the IR and IR-E groups unlike the control group. However, its numbers were significantly increased in the IR-E group unlike the IR group. TUNEL (+) cell numbers were significantly increased in the IR group unlike the control and the IR-E groups. In erdosteine treated group, TUNEL (+) cells were detected significantly less than the IR group (P

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Journal title

volume 20  issue 1

pages  53- 58

publication date 2017-01-01

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