Dorema aucheri extract for reducing oxidative stress and kidney injuries in diabetic rats

سال انتشار: 1405
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 105

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شناسه ملی سند علمی:

JR_AJP-16-4_009

تاریخ نمایه سازی: 16 تیر 1405

چکیده مقاله:

Objective: Diabetic hyperglycemia causes oxidative stress, contributing to chronic kidney disease (CKD). This study evaluated the effects of ethanolic Dorema aucheri extract from aerial parts on oxidative stress, inflammation, and kidney injury in diabetic rats.Materials and Methods: Thirty male rats were randomly assigned to five groups (n=۶): non-diabetic control, diabetic control, diabetic + metformin (۵۰۰ mg/kg/day), and diabetic + D. aucheri extract (۲۵۰ or ۵۰۰ mg/kg/day). Treatments were given orally for ۲۸ days. Serum and kidney samples were analyzed for fasting blood glucose (FBS), renal function [blood urea nitrogen (BUN), creatinine (Cr)], inflammatory cytokines [interleukin-۶ (IL-۶), interleukin-۱β (IL-۱β)], oxidative stress [malondialdehyde (MDA), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx)], mRNA expression [kidney injury molecule-۱ (KIM-۱), neutrophil gelatinase-associated lipocalin (NGAL), B-cell lymphoma ۲ (BCL-۲), Caspase-۹ (CASP-۹)], stereology, and histopathology.Results: Treatment with D. aucheri hydroalcoholic extract significantly improved metabolic, inflammatory, oxidative, and renal outcomes in diabetic rats. Specifically, both ۲۵۰ mg/kg and ۵۰۰ mg/kg doses reduced blood glucose (p<۰.۰۵), BUN (p<۰.۰۵ and p<۰.۰۱) and Cr (p<۰.۰۱ for ۵۰۰ mg/kg), IL-۶ (p<۰.۰۵), and IL-۱β (p<۰.۰۵ and p<۰.۰۰۱), respectively. MDA decreased (p<۰.۰۰۱ and p<۰.۰۵), SOD, CAT, and GPx increased (p<۰.۰۱). Renal KIM-۱ and NGAL decreased (p<۰.۰۱), CASP-۹ decreased (p<۰.۰۱ and p<۰.۰۵), and BCL-۲ increased (p<۰.۰۵), respectively. Histopathology confirmed reduced kidney damage correlating with biochemical and gene expression improvements.Conclusion: Dorema aucheri extract has the potential to modulate antioxidant and apoptotic pathways and reduce kidney injury in diabetic rats. Further studies are needed to confirm its therapeutic efficacy.

نویسندگان

Alireza Raeisi

Endocrinology and Metabolism Research Center, Shiraz University of Medical Science, Shiraz, Iran

Farhad Koohpeyma

Student research committee, Shiraz University of Medical Sciences, Shiraz, Iran

Morvarid Siri

Autophagy Research center, Shiraz University of Medical Sciences, Shiraz, Iran.

Hediye Fahandezh Saadi

Endocrinology and Metabolism Research Center, Shiraz University of Medical Science, Shiraz, Iran

Forough Saki

Endocrinology and Metabolism Research Center, Shiraz University of Medical Science, Shiraz, Iran

Golrokh Bahmani

Endocrinology and Metabolism Research Center, Shiraz University of Medical Science, Shiraz, Iran

Pardis Negaresh

Endocrinology and Metabolism Research Center, Shiraz University of Medical Science, Shiraz, Iran

Mesbah Shams

Endocrinology and Metabolism Research Center, Shiraz University of Medical Science, Shiraz, Iran

Sanaz Dastghaib

Autophagy Research center, Shiraz University of Medical Sciences, Shiraz, Iran