The protective properties of resveratrol against glycerol-induced acute kidney injury in rats

سال انتشار: 1404
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 133

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شناسه ملی سند علمی:

JR_AJP-15-1_007

تاریخ نمایه سازی: 11 دی 1403

چکیده مقاله:

Objective: After rhabdomyolysis, muscle tissue releases substances such as myoglobin, creatine kinase, and electrolytes into the bloodstream, potentially leading to acute kidney injury (AKI). Resveratrol (RSV) is a polyphenol compound with anti-inflammatory and antioxidant effects and it is found in various plants. This research evaluated the protective effects of RSV in rhabdomyolysis-induced AKI in rat kidneys.Materials and Methods: Thirty-six male Wistar rats were randomly assigned to six groups (n=۶): ۱) control (normal saline), ۲) glycerol only (۱۰ ml/kg, intramuscular), ۳, ۴, and ۵) glycerol +RSV (۵, ۱۰, and ۲۵ mg/kg, intraperitoneal injection) and ۶) RSV (۲۵ mg/kg). After ۴ days, pathological alterations and the level of blood urea nitrogen (BUN) and serum creatinine were determined. Malondialdehyde (MDA), glutathione (GSH), neutrophil gelatinase-associated lipocalin (NGAL), and tumor necrosis factor-α (TNF-α) proteins were investigated in rat kidneys. Results: Injection of ۵۰% glycerol (۱۰ ml/kg, IM) resulted in pathological lesions, elevated levels of MDA (p<۰.۰۰۱), BUN (p<۰.۰۱), serum creatinine (p<۰.۰۰۱), TNF-α (p<۰.۰۱), and NGAL protein (p<۰.۰۰۱), and decreased GSH content (p<۰.۰۰۱) compared to the control animals. These findings indicated AKI induced by rhabdomyolysis. RSV (۲۵ mg/kg) administration significantly decreased serum creatinine, BUN, MDA, NGAL, and TNF-α levels compared to the glycerol group. Histopathologically, tubule necrosis, myoglobin cast formation and glomerular atrophy increased in the glycerol group and reduced in animals that received RSV.Conclusion: In the glycerol-induced AKI rat model, RSV administration alleviated renal dysfunction by reducing oxidative stress and inflammatory responses.

نویسندگان

Mohammadreza Baghishani

Department of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran

Soghra Mehri

Department of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran

Tahereh Aminifard

Department of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran

Amirhossein Jafarian

Department of Pathology, Ghaem Hospital, Mashhad University of Medical Sciences, Mashhad, Iran

Hossein Hosseinzadeh

Department of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran