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-乙酰半胱氨酸促进2型糖尿病小鼠缺血肢体的恢复。

-Acetylcysteine Enhances the Recovery of Ischemic Limb in Type-2 Diabetic Mice.

作者信息

Zhu Qiang, Liu Xuanyou, Zhu Qingyi, Liu Zehao, Yang Chunlin, Wu Hao, Zhang Linfang, Xia Xiujuan, Wang Meifang, Hao Hong, Cui Yuqi, Zhang Guangsen, Hill Michael A, Flaker Gregory C, Zhou Shenghua, Liu Zhenguo

机构信息

Center for Precision Medicine, Department of Medicine, Division of Cardiovascular Medicine, University of Missouri School of Medicine, Columbia, MO 65212, USA.

Department of Cardiology, Second Xiangya Hospital, Central South University, Changsha 410011, China.

出版信息

Antioxidants (Basel). 2022 May 31;11(6):1097. doi: 10.3390/antiox11061097.

DOI:10.3390/antiox11061097
PMID:35739993
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9219773/
Abstract

Critical limb ischemia (CLI) is a severe complication of diabetes mellitus that occurs without effective therapy. Excessive reactive oxygen species (ROS) production and oxidative stress play critical roles in the development of diabetic cardiovascular complications. -acetylcysteine (NAC) reduces ischemia-induced ROS production. The present study aimed to investigate the effect of NAC on the recovery of ischemic limb in an experimental model of type-2 diabetes. TALLYHO/JngJ diabetic and SWR/J non-diabetic mice were used for developing a CLI model. For NAC treatment, mice received NAC (1 mg/mL) in their drinking water for 24 h before initiating CLI, and continuously for the duration of the experiment. Blood flow, mechanical function, histology, expression of antioxidant enzymes including superoxide dismutase (SOD)-1, SOD-3, glutathione peroxidase (Gpx)-1, catalase, and phosphorylated insulin receptor substrate (IRS)-1, Akt, and eNOS in ischemic limb were evaluated in vivo or ex vivo. Body weight, blood glucose, plasma advanced glycation end-products (AGEs), plasma insulin, insulin resistance index, and plasma TNF-a were also evaluated during the experiment. NAC treatment effectively attenuated ROS production with preserved expressions of SOD-1, Gpx-1, catalase, phosphorylated Akt, and eNOS, and enhanced the recovery of blood flow and function of the diabetic ischemic limb. NAC treatment also significantly decreased the levels of phosphorylated IRS-1 (Ser307) expression and plasma TNF-α in diabetic mice without significant changes in blood glucose and AGEs levels. In conclusion, NAC treatment enhanced the recovery of blood flow and mechanical function in ischemic limbs in T2D mice in association with improved tissue redox/inflammatory status and insulin resistance.

摘要

严重肢体缺血(CLI)是糖尿病的一种严重并发症,在没有有效治疗的情况下发生。过量的活性氧(ROS)生成和氧化应激在糖尿病心血管并发症的发展中起关键作用。N-乙酰半胱氨酸(NAC)可减少缺血诱导的ROS生成。本研究旨在探讨NAC对2型糖尿病实验模型中缺血肢体恢复的影响。使用TALLYHO/JngJ糖尿病小鼠和SWR/J非糖尿病小鼠建立CLI模型。对于NAC治疗,小鼠在开始CLI前24小时在饮用水中给予NAC(1mg/mL),并在实验期间持续给予。在体内或体外评估缺血肢体的血流、力学功能、组织学、抗氧化酶(包括超氧化物歧化酶(SOD)-1、SOD-3、谷胱甘肽过氧化物酶(Gpx)-1、过氧化氢酶)以及磷酸化胰岛素受体底物(IRS)-1、Akt和eNOS的表达。在实验期间还评估了体重、血糖、血浆晚期糖基化终产物(AGEs)、血浆胰岛素、胰岛素抵抗指数和血浆TNF-α。NAC治疗有效地减轻了ROS生成,同时保留了SOD-1、Gpx-1、过氧化氢酶、磷酸化Akt和eNOS的表达,并增强了糖尿病缺血肢体的血流和功能恢复。NAC治疗还显著降低了糖尿病小鼠中磷酸化IRS-1(Ser307)的表达水平和血浆TNF-α,而血糖和AGEs水平没有显著变化。总之,NAC治疗增强了T2D小鼠缺血肢体的血流和力学功能恢复,同时改善了组织氧化还原/炎症状态和胰岛素抵抗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bca/9219773/8fde1f869298/antioxidants-11-01097-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bca/9219773/8fde1f869298/antioxidants-11-01097-g008.jpg
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