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氨基糖二酸氨基酸idoBR1 可降低小胶质细胞的炎症反应。

Iminosugar Amino Acid idoBR1 Reduces Inflammatory Responses in Microglia.

机构信息

Department of Pharmacy, School of Applied Sciences, University of Huddersfield, Queensgate, Huddersfield HD1 3DH, UK.

Department of Hospital Pharmacy, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan.

出版信息

Molecules. 2022 May 23;27(10):3342. doi: 10.3390/molecules27103342.

Abstract

(1) Background. Inflammation is reported to be a key factor in neurodegeneration. The microglia are immune cells present in the central nervous system; their activation results in the release of inflammatory cytokines and is thought to be related to aging and neurodegenerative disorders, such as Alzheimer's disease. (2) Methods. A mouse BV-2 microglia cell line was activated using LPS and the anti-inflammatory cucumber-derived iminosugar amino acid idoBR1, (2,3,4,5)-3,4,5-trihydroxypiperidine-2-carboxylic acid, was used alongside dexamethasone as the control to determine whether it could reduce the inflammatory responses. (3) Results. A dose-dependent reduction in the LPS-induced production of the proinflammatory factors TNFα, IL-6, and nitric oxide and the transcription factor NF-B was found. (4) Conclusions. Further investigations of the anti-inflammatory effects of idoBR1 in other models of neurodegenerative diseases are warranted.

摘要

(1) 背景:炎症被认为是神经退行性变的关键因素。小胶质细胞是存在于中枢神经系统中的免疫细胞;其激活导致炎症细胞因子的释放,被认为与衰老和神经退行性疾病有关,如阿尔茨海默病。(2) 方法:使用 LPS 激活小鼠 BV-2 小胶质细胞系,并使用抗炎的黄瓜衍生的亚氨基糖氨基酸idoBR1(2,3,4,5)-3,4,5-三羟基哌啶-2-羧酸,与地塞米松一起作为对照,以确定它是否可以减轻炎症反应。(3) 结果:发现对 LPS 诱导的促炎因子 TNFα、IL-6 和一氧化氮和转录因子 NF-B 的产生呈剂量依赖性降低。(4) 结论:idoBR1 在其他神经退行性疾病模型中的抗炎作用值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34bb/9143674/e2360da2d025/molecules-27-03342-sch001.jpg

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