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膳食(-)-表儿茶素作为βγ-分泌酶淀粉样前体蛋白加工的有效抑制剂。

Dietary (-)-epicatechin as a potent inhibitor of βγ-secretase amyloid precursor protein processing.

作者信息

Cox Carla J, Choudhry Fahd, Peacey Eleanor, Perkinton Michael S, Richardson Jill C, Howlett David R, Lichtenthaler Stefan F, Francis Paul T, Williams Robert J

机构信息

Department of Biology and Biochemistry, University of Bath, UK.

Wolfson Centre for Age-Related Diseases, King's College London, London, UK.

出版信息

Neurobiol Aging. 2015 Jan;36(1):178-87. doi: 10.1016/j.neurobiolaging.2014.07.032. Epub 2014 Jul 30.

Abstract

Flavonoids, a group of dietary polyphenols have been shown to possess cognitive health benefits. Epidemiologic evidence suggests that they could play a role in risk reduction in dementia. Amyloid precursor protein processing and the subsequent generation of amyloid beta (Aβ) are central to the pathogenesis of Alzheimer's disease, as soluble, oligomeric Aβ is thought to be the toxic species driving disease progression. We undertook an in vitro screen to identify flavonoids with bioactivity at βγ-mediated amyloid precursor protein processing, which lead to identification of a number of flavonoids bioactive at 100 nM. Because of known bioavailability, we investigated the catechin family further and identified epigallocatechin and (-)-epicatechin as potent (nanomolar) inhibitors of amyloidogenic processing. Supporting this finding, we have shown reduced Aβ pathology and Aβ levels following short term, a 21-day oral delivery of (-)-epicatechin in 7-month-old TASTPM mice. Further, in vitro mechanistic studies suggest this is likely because of indirect BACE1 inhibition. Taken together, our results suggest that orally delivered (-)-epicatechin may be a potential prophylactic for Alzheimer's disease.

摘要

黄酮类化合物是一类膳食多酚,已被证明对认知健康有益。流行病学证据表明,它们可能在降低痴呆风险方面发挥作用。淀粉样前体蛋白的加工以及随后淀粉样β(Aβ)的产生是阿尔茨海默病发病机制的核心,因为可溶性寡聚Aβ被认为是驱动疾病进展的有毒物质。我们进行了一项体外筛选,以鉴定在βγ介导的淀粉样前体蛋白加工过程中具有生物活性的黄酮类化合物,从而鉴定出了一些在100 nM时具有生物活性的黄酮类化合物。由于已知其生物利用度,我们进一步研究了儿茶素家族,并确定表没食子儿茶素和(-)-表儿茶素是淀粉样生成加工的有效(纳摩尔)抑制剂。支持这一发现的是,我们在7个月大的TASTPM小鼠中进行了为期21天的(-)-表儿茶素口服给药后,显示出Aβ病理学和Aβ水平降低。此外,体外机制研究表明,这可能是由于间接抑制β-分泌酶1。综上所述,我们的结果表明,口服(-)-表儿茶素可能是阿尔茨海默病的一种潜在预防药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b7/4270442/bc148c6ed907/gr1.jpg

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