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黄芪甲苷补充剂通过抑制2型糖尿病小鼠的神经炎症和氧化应激来减轻认知障碍。

Astragaloside IV supplementation attenuates cognitive impairment by inhibiting neuroinflammation and oxidative stress in type 2 diabetic mice.

作者信息

Zhang Yaxuan, Yuan Yuan, Zhang Jiawei, Zhao Yao, Zhang Yueqi, Fu Jianliang

机构信息

Department of Neurology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.

出版信息

Front Aging Neurosci. 2022 Sep 29;14:1004557. doi: 10.3389/fnagi.2022.1004557. eCollection 2022.

Abstract

Although diabetic cognitive impairment is one of the most common complications of type 2 diabetes mellitus (T2DM), optimized therapeutic strategies are not available yet. Astragalosides IV (AS-IV) is a traditional Chinese medicine possessing diverse pharmacological properties including anti-inflammatory and antioxidant effects. However, the effects of AS-IV on diabetes-related cognitive impairment and its precise mechanisms remain largely unknown. T2DM mice, induced by a high-fat diet (HFD) and an intraperitoneal injection of low-dose streptozotocin (STZ) were administrated with AS-IV every other day for eight consecutive weeks. Learning and memory abilities were assessed subsequently using the Ymaze test and the anxious behavior was evaluated using an open field test. Then, the morphology and number of neurons and microglia were observed by HE staining or immunohistochemistry. Oxidative stress biomarkers and pro-inflammatory cytokines were determined using relevant kits. In addition, the expression levels of Nrf2, Keap1, HO-1, and NQO1 were determined by Western blot analyses. The results indicated that AS-IV administration significantly improved neuronal damage and cognitive deficit in T2DM mice. Meanwhile, oxidative stress and neuroinflammation were also ameliorated in T2DM mice, which might be attributed to the regulation of Nrf2/Keap1/HO-1/NQO1 pathway in T2DM mice. Taken together, these data suggested that AS-IV ameliorates cognitive impairment in T2DM mice by attenuating oxidative stress and neuroinflammation, possibly through modulating the Nrf2/Keap1/HO1/NQO1 pathway.

摘要

尽管糖尿病认知障碍是2型糖尿病(T2DM)最常见的并发症之一,但尚未有优化的治疗策略。黄芪甲苷IV(AS-IV)是一种具有多种药理特性的中药,包括抗炎和抗氧化作用。然而,AS-IV对糖尿病相关认知障碍的影响及其确切机制仍 largely unknown。通过高脂饮食(HFD)和腹腔注射低剂量链脲佐菌素(STZ)诱导的T2DM小鼠连续八周每隔一天给予AS-IV。随后使用Y迷宫试验评估学习和记忆能力,并使用旷场试验评估焦虑行为。然后,通过HE染色或免疫组织化学观察神经元和小胶质细胞的形态和数量。使用相关试剂盒测定氧化应激生物标志物和促炎细胞因子。此外,通过蛋白质印迹分析测定Nrf2、Keap1、HO-1和NQO1的表达水平。结果表明,给予AS-IV可显著改善T2DM小鼠的神经元损伤和认知缺陷。同时,T2DM小鼠的氧化应激和神经炎症也得到改善,这可能归因于对T2DM小鼠Nrf2/Keap1/HO-1/NQO1通路的调节。综上所述,这些数据表明AS-IV通过减轻氧化应激和神经炎症,可能通过调节Nrf2/Keap1/HO1/NQO1通路来改善T2DM小鼠的认知障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a454/9557080/c983663d519f/fnagi-14-1004557-g0001.jpg

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