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An experimental study of exenatide effects on renal injury in diabetic rats1.

Acta Cir Bras · 2019

Last updated 2026-05-28

In a study of 50 rats, those given the highest dose of exenatide (8 μg/kg) for 8 weeks showed lower blood sugar levels, improved insulin, and reduced kidney damage markers compared to untreated diabetic rats. The treated rats also had less oxidative stress and inflammation in their kidney tissue, suggesting exenatide may help protect against kidney injury in diabetes.

AI summary of the abstract below.

JournalActa Cir Bras, 2019
Citations19
Relative citation ratio0.99
NIH percentile50
Molecules exenatide
Conditions studied Type 2 Diabetes, Chronic Kidney Disease

Abstract

PURPOSE: To investigate the effects of exenatide on renal injury in streptozotocin-induced diabetic rats. METHODS: Fifty SD rats were randomly divided into normal control, model, exenatide-1, exenatide-2 and exenatide-3 groups, 10 rats in each group. The diabetic nephropathy model was constructed in later 4 groups. Then, the later 3 groups were treated with 2, 4 and 8 μg/kg exenatide for 8 weeks, respectively. The serum and urine biochemical indexes and oxidative stress and inflammatory indexes in renal tissue were determined. RESULTS: Compared to the model group, in exenatide-3 group the serum fasting plasma glucose and hemoglobin A1c levels were significantly decreased, the fasting insulin level was significantly increased, the renal index and blood urea nitrogen, serum creatinine and 24 h urine protein levels were significantly decreased, the renal tissue superoxide dismutase and glutathione peroxidase levels were significantly increased, the malondialdehyde level was significantly decreased, and the renal tissue tumor necrosis factor alpha, interleukin 6, hypersensitive C-reactive protein and chemokine (C-C motif) ligand 5 levels were significantly decreased P<0.05). CONCLUSIONS: Exenatide can mitigate the renal injury in diabetic rats. The mechanisms may be related to its resistance of oxidative stress and inflammatory response in renal tissue.

Verbatim abstract via PubMed 30785502 ↗

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