Yu Bo, Jiang Yu, Jin Lingling, Ma Tonghui, Yang Hong
Liaoning Provincial Key Laboratory of Biotechnology and Drug Discovery, School of Life Sciences, Liaoning Normal University Dalian, China.
College of Basic Medical Sciences, Dalian Medical University Dalian, China.
Front Physiol. 2016 Nov 23;7:549. doi: 10.3389/fphys.2016.00549. eCollection 2016.
Epithelial chloride channels provide the pathways for fluid secretion in the intestine. Cystic fibrosis transmembrane conductance regulator (CFTR) and calcium-activated chloride channels (CaCCs) are the main chloride channels in the luminal membrane of enterocytes. These transmembrane proteins play important roles in many physiological processes. In this study, we have identified a flavonoid quercetin as a modulator of CaCC chloride channel activity. Fluorescence quenching assay showed that quercetin activated Cl transport in a dose-dependent manner, with EC ~37 μM. Short-circuit current analysis confirmed that quercetin activated CaCC-mediated Cl currents in HT-29 cells that can be abolished by CaCC-A01. studies indicated that application of quercetin to mouse ileum and colon on serosal side resulted in activation of CFTR and CaCC-mediated Cl currents. Notably, we found that quercetin exhibited inhibitory effect against ANO1 chloride channel activity in ANO1-expressing FRT cells and decreased mouse intestinal motility. Quercetin-stimulated short-circuit currents in mouse ileum was multi-component, which included elevation of Ca concentration through L-type calcium channel and activation of basolateral NKCC, Na/K-ATPase, and K channels. studies further revealed that quercetin promoted fluid secretion in mouse ileum. The modulatory effect of quercetin on CaCC chloirde channels may therefore represent a potential therapeutic strategy for treating CaCC-related diseases like constipation, secretory diarrhea and hypertension. The inverse effects of quercetin on CaCCs provided evidence that ANO1 and intestinal epithelial CaCCs are different calcium-activated chloride channels.
上皮氯离子通道为肠道中的液体分泌提供了途径。囊性纤维化跨膜传导调节因子(CFTR)和钙激活氯离子通道(CaCCs)是肠上皮细胞腔面膜中的主要氯离子通道。这些跨膜蛋白在许多生理过程中发挥着重要作用。在本研究中,我们鉴定出黄酮类化合物槲皮素是CaCC氯离子通道活性的调节剂。荧光猝灭分析表明,槲皮素以剂量依赖的方式激活氯离子转运,其半数有效浓度(EC)约为37μM。短路电流分析证实,槲皮素可激活HT - 29细胞中CaCC介导的氯离子电流,而该电流可被CaCC - A01消除。研究表明,将槲皮素应用于小鼠回肠和结肠的浆膜侧可激活CFTR和CaCC介导的氯离子电流。值得注意的是,我们发现槲皮素对表达ANO1的FRT细胞中的ANO1氯离子通道活性具有抑制作用,并降低了小鼠的肠道蠕动。槲皮素刺激的小鼠回肠短路电流是多组分的,其中包括通过L型钙通道升高钙浓度以及激活基底外侧的NKCC、Na/K - ATP酶和钾通道。研究进一步表明,槲皮素促进了小鼠回肠中的液体分泌。因此,槲皮素对CaCC氯离子通道的调节作用可能代表了一种治疗便秘、分泌性腹泻和高血压等与CaCC相关疾病的潜在治疗策略。槲皮素对CaCCs的相反作用提供了证据,表明ANO1和肠上皮CaCCs是不同的钙激活氯离子通道。