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海藻糖对锰诱导的小鼠α-突触核蛋白寡聚化的保护作用:涉及氧化应激和自噬。

Protective effects of trehalose against Mn-induced α-synuclein oligomerization in mice: Involvement of oxidative stress and autophagy.

机构信息

Department of Environmental Health, School of Public Health, China Medical University, Shenyang, People's Republic of China.

出版信息

Environ Toxicol. 2020 Jan;35(1):55-65. doi: 10.1002/tox.22842. Epub 2019 Sep 9.

Abstract

Overexposure to manganese (Mn) is widely known to induce alpha-synuclein (α-Syn) oligomerization, which has been attributed to the oxidative damage of α-Syn protein. Trehalose has been shown to induce autophagy and serve as a chemical chaperone, but little information has been reported about its effect on Mn-induced α-Syn oligomerization. In this study, we investigate whether trehalose can effectively interfere with Mn-induced α-Syn oligomerization, using different concentrations of trehalose (2% and 4% (g/vol [mL])) in a mouse model of manganism. After 6 weeks of exposure to Mn, both oxidative stress and autophagy were activated and resulted in α-Syn oligomerization and neuronal cell damage in the mouse brain tissue. Our results also revealed that pretreatment with trehalose significantly reduced the oxidative damage to α-Syn protein and increased autophagy activation. These findings clearly demonstrated that trehalose can relieve Mn-induced α-Syn oligomerization and neuronal cell damage through its anti-oxidative and autophagy-inducing effects.

摘要

过量的锰(Mn)暴露会广泛诱导α-突触核蛋白(α-Syn)寡聚化,这归因于α-Syn 蛋白的氧化损伤。海藻糖已被证明可诱导自噬并作为化学伴侣,但关于其对 Mn 诱导的α-Syn 寡聚化的影响的信息却很少。在这项研究中,我们使用不同浓度的海藻糖(2%和 4%(g/vol [mL]))在锰中毒的小鼠模型中研究了海藻糖是否可以有效干扰 Mn 诱导的α-Syn 寡聚化。在暴露于 Mn 6 周后,氧化应激和自噬都被激活,导致小鼠脑组织中的α-Syn 寡聚化和神经元细胞损伤。我们的结果还表明,海藻糖预处理可显著减轻α-Syn 蛋白的氧化损伤并增加自噬的激活。这些发现清楚地表明,海藻糖可以通过其抗氧化和诱导自噬作用来缓解 Mn 诱导的α-Syn 寡聚化和神经元细胞损伤。

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