gsk -3 β抑制剂诱导Nrf2/TrxR2信号通路表达对糖尿病大鼠肾缺血再灌注损伤的保护作用

Bo Hu, Yuhong Wu, Jie Liu, Xiaohua Shen, F. Tong, Guangtao Xu, R. Shen
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引用次数: 49

摘要

背景/目的:糖尿病(DM)可导致肾脏损害和功能障碍,加重肾缺血/再灌注损伤(RI/RI)。本研究旨在探讨GSK-3β抑制剂TDZD-8通过Nrf2/TrxR2信号通路对大鼠DM模型中RI/RI的保护作用。方法:单次注射链脲佐菌素建立DM大鼠模型。用TDZD-8 (1 mg/kg bw)或TDZD-8+金醛脂(10 nmol/L, 5ml/kg bw)预处理糖尿病大鼠,缺血45 min,再灌注24 h。将大鼠随机分为4组:假手术组、RI/RI组、TDZD-8组和TDZD-8+金糠蛋白组。测定血清BUN和Scr水平。测定大鼠肾组织中SOD活性、MDA含量及Nrf2、TrxR2、caspase-3的表达。结果:TDZD-8处理大鼠的肾功能得到改善,氧化应激和细胞凋亡减少,Nrf2和TrxR2的表达上调。结论:TDZD-8可能通过调节DM肾组织Nrf2/TrxR2信号通路发挥对RI/RI的保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GSK-3beta Inhibitor Induces Expression of Nrf2/TrxR2 Signaling Pathway to Protect against Renal Ischemia/Reperfusion Injury in Diabetic Rats
Background/Aims: Diabetes mellitus (DM) can lead to renal damage and dysfunction, and exacerbate renal ischemia/reperfusion injury (RI/RI). The aim of this study was to investigate the protective effect of GSK-3β inhibitor TDZD-8 against RI/RI through Nrf2/TrxR2 signaling pathway in a rat DM model. Methods: A DM rat model was established by a single injection of streptozocin. Diabetic rats were pretreated with TDZD-8 (1 mg/kg bw) or TDZD-8+auranofin (10 nmol/L, 5ml/kg bw), and then subjected to 45-min ischemia and 24-h reperfusion. Rats were equally randomized into four groups: a Sham-operated group, a RI/RI group, a TDZD-8 group, and a TDZD-8+auranofin group. Serum levels of BUN and Scr were measured. SOD activity, MDA content, and Nrf2, TrxR2 and caspase-3 expressions in rat kidney tissues were determined. Results: Renal function was improved, oxidative stress and cell apoptosis were reduced, and the expression of Nrf2 and TrxR2 was up-regulated in TDZD-8 treated rats as compared with those in auranofin treated rats. Conclusion: TDZD-8 may exert its protective effect against RI/RI by regulating the Nrf2/TrxR2 signaling pathway in the kidney tissue in DM.
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