THE POTENTIAL MODULATING IMPACT OF THE DIPEPTIDYL PEPTIDASE-4 (DPP-4) INHIBITOR, SITAGLIPTIN ON STREPTOZOTOCIN-NICOTINAMIDE-INDUCED DIABETIC NEPHROPATHY IN RATS | ||||
Bulletin of Pharmaceutical Sciences Assiut University | ||||
Volume 45, Issue 2, December 2022, Page 1013-1026 PDF (1000.94 K) | ||||
Document Type: Original Article | ||||
DOI: 10.21608/bfsa.2022.271787 | ||||
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Authors | ||||
Ahmed O. Abdel-Zaher1; Marwa G. Abd-Allah1; Ghada H. Mohammad2; Rania Abdel-Emam 3 | ||||
1Department of Pharmacology, Faculty of Medicine, Assiut University, Assiut 71526, Egypt | ||||
2Department of Pathology, Faculty of Medicine, Assiut University, Assiut 71526, Egypt | ||||
3Pharmacology Department, Faculty of Medicine, Assiut University, Assiut, Egypt | ||||
Abstract | ||||
The main risk factor for the onset and development of diabetic nephropathy (DN) is hyperglycemia. Kidney end-stage disease is brought on by DN, a significant microvascular consequence of diabetes. In this study, we evaluated the renoprotective potential of sitagliptin in a rat model of streptozotocin-nicotinamide-induced DN. Following the intraperitoneal treatment of rats with 110 mg/kg nicotinamide followed 15 min by 60 mg/kg streptozotocin, DN manifested in rats after 8 weeks. Fasting blood glucose, postprandial blood glucose, HbA1c, serum urea and creatinine, and urine albumin levels were assessed in control, DN, and DN rats treated with sitagliptin. Additionally, paraffin-embedded kidney segment histopathological assessment was carried out. The increased levels of fasting, postprandial blood glucose, and HbA1c were decreased with sitagliptin. Sitagliptin restored the changes in kidney structure and function brought on by DN. The findings suggest that sitagliptin could prevent DN by stringent glycemic management, restoring the kidneys' declining function and protecting their structure. | ||||
Keywords | ||||
Streptozotocin; Diabetic nephropathy; Sitagliptin; Kidney function and structure | ||||
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