[槲皮素通过抑制 HMGB1/RAGE/NF-κB 信号通路改善大鼠的糖尿病肾损伤]

Q3 Medicine
Y Jiang, X Li, J Geng, Y Chen, B Tang, P Kang
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引用次数: 0

摘要

目的:探讨槲皮素对糖尿病大鼠肾脏炎症和细胞凋亡的影响及其可能机制:探讨槲皮素对糖尿病大鼠肾脏炎症和细胞凋亡的影响及其可能机制:将24只成年雄性SD大鼠随机平均分为正常对照组、高糖高脂喂养组、链脲佐菌素(STZ)诱导的糖尿病模型组和槲皮素治疗组(日剂量100 mg/kg)。大鼠肾组织的病理变化采用 HE 染色法观察,血清炎症因子水平采用 ELISA 法测定,NF-κB 的表达采用免疫组化法观察。测定大鼠的快餐血糖(FBG)、血清甘油三酯(TG)、BUN、Scr水平和24小时尿蛋白含量,并用Western印迹法检测肾脏中HMGB1、RAGE、NF-κB、Bax、Bcl-2和caspase-3的表达:结果:糖尿病大鼠的 FBG、TG、BUN 和 Scr 水平、肾脏肥大指数、24 小时尿蛋白含量、血清 IL-1β、IL-6 和 TNF-α 水平以及肾脏中 HMGB1、RAGE、NF-κB、Bax 和 caspase-3 的表达均显著升高,而肾脏中 Bcl-2 的表达降低。槲皮素治疗大鼠后可明显缓解所有这些变化:结论:槲皮素能减轻糖尿病大鼠的肾损伤,可能是通过抑制 HMGB1/RAGE/NF-κB 炎症信号通路来减轻肾炎症和肾细胞凋亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Quercetin ameliorates diabetic kidney injury in rats by inhibiting the HMGB1/RAGE/NF-κB signaling pathway].

Objective: To explore the effect of quercetin on renal inflammation and cell apoptosis in diabetic rats and its possible mechanisms.

Methods: Twenty-four adult male SD rats were randomized equally into normal control group, high-glucose and high-fat feeding group, streptozotocin (STZ) -induced diabetic model group, and quercetin treatment (daily dose 100 mg/kg) group. Pathological changes of the renal tissues of the rats were observed with HE staining, serum inflammatory factor levels were determined with ELISA, and renal expression of NF‑κB was observed by immunohistochemistry. Fast blood glucose (FBG), serum levels of triglyceride (TG), BUN, and Scr, and 24-h urine protein content of the rats were measured, and renal expressions of HMGB1, RAGE, NF‑κB, Bax, Bcl-2, and caspase-3 were detected with Western blotting.

Results: The diabetic rats showed significantly increased levels of FBG, TG, BUN, and Scr, renal hypertrophy index, 24-h urinary protein content, serum IL-1β, IL-6 and TNF-α levels and renal expressions HMGB1, RAGE, NF‑κB, Bax, and caspase-3 with decreased renal expression of Bcl-2. All these changes were significantly alleviated by quercetin treatment of the rats.

Conclusion: Quercetin can ameliorate kidney injury in diabetic rats possibly by inhibiting the HMGB1/RAGE/NF-κB inflammatory signaling pathway to reduce renal inflammation and renal cell apoptosis.

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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
208
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