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