椭圆素通过抑制氧化应激和炎症介质对链脲佐菌素诱导的糖尿病肾病大鼠的肾保护作用。

Acta cirurgica brasileira Pub Date : 2023-12-04 eCollection Date: 2023-01-01 DOI:10.1590/acb385623
Jun Li, Yu Xie, Jimei Sun, Fan Bai, Shaik Althaf Hussain, Venkata Subba Reddy Gangireddygari, Xiaolan Jiang
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引用次数: 0

摘要

目的:糖尿病是世界范围内严重的健康问题,糖尿病肾病是糖尿病的并发症。糖尿病肾病显著增强氧化应激、糖基化、脂质参数和炎症反应。Ellipticine具有清除自由基和抗炎的作用。方法:在本研究中,我们的目的是深入研究椭圆素在链脲佐菌素(STZ)诱导的糖尿病肾病(DN)大鼠模型中的肾脏保护作用,并阐明其潜在机制。为了诱导糖尿病肾病,采用链脲佐菌素(50 mg/kg),并将大鼠分成不同组,给予不同剂量的椭圆素(2.5、5和7.5 mg/kg)。估计体重和肾脏重量。评估炎症因子、肾脏生物标志物、炎症抗氧化剂和尿液参数。结果:结果表明,椭圆素能显著提高大鼠体重,减轻肾组织重量。椭圆替辛治疗显著(P < 0.001)降低了血清尿素氮、肌酐、尿酸、血糖水平,并改变了血脂参数。Ellipticine显著(P < 0.001)抑制丙二醛水平,提高谷胱甘肽、过氧化氢酶、超氧化物歧化酶和谷胱甘肽过氧化物酶水平。Ellipticine治疗显著(P < 0.001)降低了炎症因子和炎症介质。结论:椭圆替辛可能通过减轻链脲佐菌素诱导大鼠的炎症反应、纤维化和氧化应激而具有肾保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Renal protective effect of ellipticine against streptozotocin induced diabetic nephropathy in rats via suppression of oxidative stress and inflammatory mediator.

Purpose: Diabetes mellitus is a serious health problem worldwide, and diabetic nephropathy is the complication. The diabetic nephropathy considerably enhances the oxidative stress, glycation, lipid parameters and inflammatory reaction. Ellipticine has potent free radical scavenging and anti-inflammatory effect.

Methods: In the current study, our objectives were to thoroughly examine the renal protective effects of ellipticine in a rat model of streptozotocin (STZ)-induced diabetic nephropathy (DN) and to elucidate the underlying mechanisms involved. For the induction of diabetic nephropathy, streptozotocin (50 mg/kg) was used, and rats were separated into groups and given varying doses of ellipticine (2.5, 5 and 7.5 mg/kg). The body weight, and renal weight were estimated. The inflammatory cytokines, renal biomarkers, inflammatory antioxidant, and urine parameters were estimated.

Results: Result showed that ellipticine considerably enhanced the body weight and reduced the renal tissue weight. Ellipticine treatment significantly (P < 0.001) repressed the level of blood urea nitrogen, serum creatinine, uric acid, blood glucose and altered the lipid parameters. Ellipticine significantly (P < 0.001) repressed the level of malonaldehyde and boosted the glutathione, catalase, superoxide dismutase, and glutathione peroxidase. Ellipticine treatment significantly (P < 0.001) reduced the inflammatory cytokines and inflammatory mediators.

Conclusions: Ellipticine could be a renal protective drug via attenuating the inflammatory reaction, fibrosis and oxidative stress in streptozotocin induced rats.

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