Renoprotective effect of thymoquinone against rhabdomyolysis-induced acute kidney injury in the rat model

سال انتشار: 1403
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 307

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شناسه ملی سند علمی:

JR_IJBMS-27-5_004

تاریخ نمایه سازی: 19 اسفند 1402

چکیده مقاله:

Objective(s): Rhabdomyolysis leads to the release of myoglobin, sarcoplasmic proteins, and electrolytes into the blood circulation causing acute kidney injury (AKI). Thymoquinone, a natural compound found in Nigella sativa seeds, has antioxidant and anti-inflammatory effects. This investigation assessed the renoprotective effect of thymoquinone on rhabdomyolysis-induced AKI in rats.Materials and Methods: Male Wistar rats were categorized into six groups (n = ۶): ۱. Control: (normal saline), ۲. Glycerol (۵۰ ml/kg, single dose, IM), ۳–۵: Glycerol + thymoquinone (۱, ۲.۵ and ۵ mg/kg, ۴ days, IP), ۶. Thymoquinone (۵ mg/kg). On day ۵, serum and kidney tissue were isolated and the amounts of serum creatinine and blood urea nitrogen (BUN), renal malondialdehyde (MDA), glutathione (GSH.), tumor necrosis factor-alpha (TNF-α), neutrophil gelatinase-associated lipocalin (NGAL), and pathological changes were evaluated. Results: Glycerol increased creatinine, BUN, MDA, TNF-α, and NGAL levels. It decreased GSH amounts and caused renal tubular necrosis, glomerular atrophy, and myoglobin cast in kidney tissue. Co-administration of glycerol and thymoquinone reduced creatinine, BUN, histopathological alterations, and MDA levels, and enhanced GSH amounts. Administration of glycerol and thymoquinone (۵ mg/kg) had no significant effect on TNF-α amount but decreased NGAL protein levels. The administration of thymoquinone (۵ mg/kg) alone did not display a significant difference from the control group.Conclusion: Rhabdomyolysis from glycerol injection in rats can cause kidney damage. Thymoquinone may attenuate renal dysfunction and oxidative stress. However, the TNF-α level was not significantly affected. Further studies are needed to explore the potential therapeutic effects of thymoquinone in managing AKI.

نویسندگان

Arezoo Hosseini

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

Mahboobeh Ghasemzadeh Rahbardar

Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran

Sadaf Nouripor

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

Abolfazl Khajavirad

Department of Physiology, School of Medicine, 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

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