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α-硫辛酸对 Aβ 诱导的 BV2 细胞损伤的神经保护作用。

Neuroprotective Effect of α-Lipoic Acid against Aβ-Induced Damage in BV2 Cells.

机构信息

National Institutes for Food and Drug Control, Beijing 100052, China.

School of Public Health, Hengyang Medical School, University of South China, Hengyang 421001, China.

出版信息

Molecules. 2023 Jan 24;28(3):1168. doi: 10.3390/molecules28031168.

Abstract

The prevalence of Alzheimer's disease (AD) is significantly increasing due to the aging world population, and the currently available drug treatments cannot cure or even slow its progression. α-lipoic acid (LA) is a biological factor widely found in spinach and meat and can dissolve in both lipid and aqueous phases. In medicine, LA has been shown to reduce the symptoms of diabetic polyneuropathy, acute kidney injury, cancers, and some metabolism-related diseases. This study to proves that α-lipoic acid (LA) can stabilize the cognitive function of patients with Alzheimer's disease (AD). BV2 cells were divided into control, LA, Aβ, and LA + Aβ groups. Cell growth; IL-6, IL-1β, TNF-α, IFN-γ, SOD, GPx, CAT, ROS, NO, and iNOS secretion; Wnt-related proteins; cell apoptosis; and cell activation were examined. Here, we found that LA could effectively repress apoptosis and changes in the morphology of microglia BV2 cells activated by Aβ, accompanied by the inhibition of the inflammatory response induced by Aβ The Wnt/β-catenin pathway is also involved in preventing Aβ-induced cytotoxicity in microglia by LA. We found an inhibitory effect of LA on microglia toxicity induced by Aβ, suggesting that a combination of anti-inflammatory and antioxidant substances may offer a promising approach to the treatment of AD.

摘要

由于世界人口老龄化,阿尔茨海默病(AD)的患病率显著增加,而目前可用的药物治疗方法既不能治愈,甚至也不能减缓其进展。α-硫辛酸(LA)是一种广泛存在于菠菜和肉类中的生物因子,可溶解于脂相和水相。在医学上,LA 已被证明可减轻糖尿病多发性神经病、急性肾损伤、癌症和一些与代谢相关的疾病的症状。本研究旨在证明 α-硫辛酸(LA)可以稳定阿尔茨海默病(AD)患者的认知功能。将 BV2 细胞分为对照组、LA 组、Aβ 组和 LA+Aβ 组。检测细胞生长;IL-6、IL-1β、TNF-α、IFN-γ、SOD、GPx、CAT、ROS、NO 和 iNOS 分泌;Wnt 相关蛋白;细胞凋亡;和细胞激活。在这里,我们发现 LA 可以有效抑制 Aβ 激活的 BV2 细胞微胶质细胞的凋亡和形态变化,同时抑制 Aβ 诱导的炎症反应。Wnt/β-连环蛋白通路也参与了 LA 防止 Aβ 诱导的微胶质细胞毒性。我们发现 LA 对 Aβ 诱导的微胶质细胞毒性有抑制作用,这表明抗炎和抗氧化物质的联合使用可能为 AD 的治疗提供一种有前途的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd92/9919339/a660ba66f151/molecules-28-01168-g001.jpg

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