Suppr超能文献

对止泻中药红景天进行生物活性导向的分离,发现(-)-表儿茶素-3-没食子酸酯和(-)-表没食子儿茶素-3-没食子酸酯是囊性纤维化跨膜传导调节因子的抑制剂。

Bioactivity-guided fractionation of an antidiarrheal Chinese herb Rhodiola kirilowii (Regel) Maxim reveals (-)-epicatechin-3-gallate and (-)-epigallocatechin-3-gallate as inhibitors of cystic fibrosis transmembrane conductance regulator.

作者信息

Chen Lei, Yu Bo, Zhang Yaofang, Gao Xin, Zhu Liang, Ma Tonghui, Yang Hong

机构信息

School of Life Sciences, Liaoning Provincial Key Laboratory of Biotechnology and Drug Discovery, Liaoning Normal University, Dalian, 116029, P. R. China.

College of Basic Medical Sciences, Dalian Medical University, Dalian, 116044, P. R. China.

出版信息

PLoS One. 2015 Mar 6;10(3):e0119122. doi: 10.1371/journal.pone.0119122. eCollection 2015.

Abstract

Cystic fibrosis transmembrane conductance regulator (CFTR) is the principal apical route for transepithelial fluid transport induced by enterotoxin. Inhibition of CFTR has been confirmed as a pharmaceutical approach for the treatment of secretory diarrhea. Many traditional Chinese herbal medicines, like Rhodiola kirilowii (Regel) Maxim, have long been used for the treatment of secretory diarrhea. However, the active ingredients responsible for their therapeutic effectiveness remain unknown. The purpose of this study is to identify CFTR inhibitors from Rhodiola kirilowii (Regel) Maxim via bioactivity-directed isolation strategy. We first identified fractions of Rhodiola kirilowii (Regel) Maxim that inhibited CFTR Cl- channel activity. Further bioactivity-directed fractionation led to the identification of (-)-epigallocatechin-3-gallate (EGCG) as CFTR Cl- channel inhibitor. Analysis of 5 commercially available EGCG analogs including (+)-catechins (C), (-)-epicatechin (EC), (-)-epigallocatechin (EGC), (-)-epicatechin-3-gallate (ECG) and EGCG revealed that ECG also had CFTR inhibitory activity. EGCG dose-dependently and reversibly inhibited CFTR Cl- channel activity in transfected FRT cells with an IC50 value around 100 μM. In ex vivo studies, EGCG and ECG inhibited CFTR-mediated short-circuit currents in isolated rat colonic mucosa in a dose-dependent manner. In an intestinal closed-loop model in mice, intraluminal application of EGCG (10 μg) and ECG (10 μg) significantly reduced cholera toxin-induced intestinal fluid secretion. CFTR Cl- channel is a molecular target of natural compounds EGCG and ECG. CFTR inhibition may account, at least in part, for the antidiarrheal activity of Rhodiola kirilowii (Regel) Maxim. EGCG and ECG could be new lead compounds for development of CFTR-related diseases such as secretory diarrhea.

摘要

囊性纤维化跨膜传导调节因子(CFTR)是肠毒素诱导的跨上皮液体运输的主要顶端途径。抑制CFTR已被确认为治疗分泌性腹泻的一种药物方法。许多传统中药,如红景天,长期以来一直用于治疗分泌性腹泻。然而,其治疗效果的活性成分尚不清楚。本研究的目的是通过生物活性导向分离策略从红景天中鉴定CFTR抑制剂。我们首先鉴定了红景天中抑制CFTR氯离子通道活性的组分。进一步的生物活性导向分级分离导致鉴定出(-)-表没食子儿茶素-3-没食子酸酯(EGCG)作为CFTR氯离子通道抑制剂。对5种市售的EGCG类似物进行分析,包括(+)-儿茶素(C)、(-)-表儿茶素(EC)、(-)-表没食子儿茶素(EGC)、(-)-表儿茶素-3-没食子酸酯(ECG)和EGCG,结果显示ECG也具有CFTR抑制活性。EGCG在转染的FRT细胞中剂量依赖性且可逆地抑制CFTR氯离子通道活性,IC50值约为100μM。在体外研究中,EGCG和ECG以剂量依赖性方式抑制分离的大鼠结肠黏膜中CFTR介导的短路电流。在小鼠肠封闭环模型中,腔内应用EGCG(10μg)和ECG(10μg)显著减少霍乱毒素诱导的肠液分泌。CFTR氯离子通道是天然化合物EGCG和ECG的分子靶点。CFTR抑制可能至少部分解释了红景天的止泻活性。EGCG和ECG可能是开发CFTR相关疾病如分泌性腹泻的新先导化合物。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验