Author/Authors :
Rofaeil ، Remon Roshdy Department of Pharmacology - Faculty of Medicine - Minia University , Ahmed ، Sabreen Mahmoud Depatment of Human Anatomy and Embryology - Faculty of Medicine - Minia University , Bahaa ، Haitham Ahmed Department of Obstetrics and Gynecology - Faculty of Medicine - Minia University , Mahran ، Ahmad Department of Obstetrics and Gynecology - Faculty of Medicine - Minia University , Welson ، Nermeen N. Department of Forensic medicine and clinical toxicology - Faculty of Medicine - Beni-Suef University , Abdelzaher ، Walaa Yehia Department of Pharmacology - Faculty of Medicine - Minia University
Abstract :
Objective(s): Uterine ischemia is a common problem with ongoing controversy about its pathogenesis and prevention. The present study aimed to investigate the protective role of sitagliptin against uterine ischemia- reperfusion injury (IRI). Materials and Methods: Rats were allocated into 4 groups: control, sitagliptin (SIT) (5 mg/kg), IR; ischemia was induced followed by reperfusion, and IR+SIT; SIT was administered 1 hr before IRI. Uteri were removed for histopathological and biochemical observations. Malondialdehyde (MDA), total nitrites (NOx), reduced glutathione (GSH), superoxide dismutase (SOD) activity, tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and toll- like receptor 4 (TLR4) were all measured. Hematoxylin and eosin (H E) stain, Periodic acid-Schiff stain (PAS), and caspase-3 immunostaining were applied. Results: In the IR+SIT group; NOx, GSH, and SOD activities increased significantly. Meanwhile, the levels of MDA, TNF-α, IL-6, TLR4, and caspase-3 immunoexpression showed a significant reduction, as compared with the IR group. In the IR+SIT group, an improvement in the histopathological picture was noticed.Conclusion: The results showed that sitagliptin confers protection against uterine IRI through anti-oxidant, anti-inflammatory, and anti-apoptotic effects with a possible role for TLR4.
Keywords :
Anti , apoptotic , Anti , inflammatory , Sitagliptin , Toll , like receptor 4 , Uterine ischemia