首页> 美国卫生研究院文献>Molecules >Synergistic Inhibition of Acetylcholinesterase by Alkaloids Derived from Stephaniae Tetrandrae Radix Coptidis Rhizoma and Phellodendri Chinensis Cortex
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Synergistic Inhibition of Acetylcholinesterase by Alkaloids Derived from Stephaniae Tetrandrae Radix Coptidis Rhizoma and Phellodendri Chinensis Cortex

机译:Stephaniae Tetrandrae板蓝根黄连和黄柏皮层生物碱对乙酰胆碱酯酶的协同抑制作用

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摘要

Alkaloids having acetylcholinesterase (AChE) inhibitory activity are commonly found in traditional Chinese medicine (TCM); for example, berberine from , galantamine from , and huperzine A from . In practice of TCM, Stephaniae Tetrandrae Radix (STR) is often combined with Coptidis Rhizoma (CR) or Phellodendri Chinensis Cortex (PCC) as paired herbs during clinical application. Fangchinoline from STR and coptisine and/or berberine from CR and/or PCC are active alkaloids in inhibiting AChE. The traditional usage of paired herbs suggests the synergistic effect of fangchinoline–coptisine or fangchinoline–berberine pairing in AChE inhibition. HPLC was applied to identify the main components in herbal extracts of STR, CR, and PCC, and the AChE inhibition of their main components was determined by Ellman assay. The synergism of herb combination and active component combination was calculated by median-effect principle. Molecular docking was applied to investigate the underlying binding mechanisms of the active components with the AChE protein. It was found that fangchinoline showed AChE inhibitory potency; furthermore, fangchinoline–coptisine/berberine pairs (at ratios of 1:5, 1:2, 1:1, and 2:1) synergistically inhibited AChE; the combination index (CI) at different ratios was less than one when = 0.5, suggesting synergistic inhibition of AChE. Furthermore, the molecular docking simulation supported this enzymatic inhibition. Therefore, fangchinoline–coptisine/berberine pairs, or their parental herbal mixtures, may potentially be developed as a possible therapeutic strategy for Alzheimer’s patients.
机译:具有乙酰胆碱酯酶(AChE)抑制活性的生物碱常见于中药(TCM)中。例如,来自的小ber碱,加兰他敏和来自的石杉碱A。在中医实践中,在临床应用过程中,千金藤(STR)通常与黄连(CR)或黄柏(PCC)组合为成对草药。 STR中的芳基胆碱和CR和/或PCC中的黄连和/或小ber碱是抑制AChE的活性生物碱。配对草药的传统用法表明,在AChE抑制中,房车碱-可的碱或房车碱-小ber碱配对具有协同作用。 HPLC用于鉴定STR,CR和PCC草药提取物中的主要成分,并通过Ellman分析测定其对AChE的主要成分的抑制作用。采用中效原理计算了中草药组合与活性成分组合的协同作用。分子对接应用于研究活性成分与AChE蛋白的潜在结合机制。结果发现,房车茶碱具有抑制AChE的能力。此外,房车茶碱-可的松/小ber碱对(比例为1:5、1:2、1:1和2:1)具有协同抑制AChE的作用。当= 0.5时,不同比率的组合指数(CI)小于1,表明对AChE有协同抑制作用。此外,分子对接模拟支持了这种酶促抑制作用。因此,可能会开发出房车碱-可的松/小ber碱对或其父母本草混合物,作为阿尔茨海默氏病患者的一种可能的治疗策略。

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