Department of Medicine , University of California, San Francisco, CA 94143-0521, USA.
FASEB J. 2010 Nov;24(11):4178-86. doi: 10.1096/fj.10-160648. Epub 2010 Jun 25.
TMEM16A was found recently to be a calcium-activated Cl(-) channel (CaCC). CaCCs perform important functions in cell physiology, including regulation of epithelial secretion, cardiac and neuronal excitability, and smooth muscle contraction. CaCC modulators are of potential utility for treatment of hypertension, diarrhea, and cystic fibrosis. Screening of drug and natural product collections identified tannic acid as an inhibitor of TMEM16A, with IC(50) ∼ 6 μM and ∼100% inhibition at higher concentrations. Tannic acid inhibited CaCCs in multiple cell types but did not affect CFTR Cl(-) channels. Structure-activity analysis indicated the requirement of gallic or digallic acid substituents on a macromolecular scaffold (gallotannins), as are present in green tea and red wine. Other polyphenolic components of teas and wines, including epicatechin, catechin, and malvidin-3-glucoside, poorly inhibited CaCCs. Remarkably, a 1000-fold dilution of red wine and 100-fold dilution of green tea inhibited CaCCs by >50%. Tannic acid, red wine, and green tea inhibited arterial smooth muscle contraction and intestinal Cl(-) secretion. Gallotannins are thus potent CaCC inhibitors whose biological activity provides a potential molecular basis for the cardioprotective and antisecretory benefits of red wine and green tea.
TMEM16A 最近被发现是一种钙激活氯离子通道(CaCC)。CaCCs 在细胞生理学中发挥着重要的功能,包括调节上皮细胞分泌、心脏和神经元兴奋性以及平滑肌收缩。CaCC 调节剂对于治疗高血压、腹泻和囊性纤维化具有潜在的应用价值。药物和天然产物库的筛选发现鞣酸是 TMEM16A 的抑制剂,IC50 约为 6 μM,在更高浓度下抑制率约为 100%。鞣酸抑制多种细胞类型中的 CaCCs,但不影响 CFTR 氯离子通道。结构活性分析表明需要在大分子支架(鞣花单宁)上具有没食子酸或二没食子酸取代基,这存在于绿茶和红酒中。茶和酒中的其他多酚成分,包括表儿茶素、儿茶素和矢车菊素-3-葡萄糖苷,对 CaCCs 的抑制作用较差。值得注意的是,红酒的 1000 倍稀释液和绿茶的 100 倍稀释液对 CaCCs 的抑制作用超过 50%。鞣酸、红酒和绿茶抑制动脉平滑肌收缩和肠道氯离子分泌。因此,鞣花单宁是一种有效的 CaCC 抑制剂,其生物学活性为红酒和绿茶的心脏保护和抗分泌作用提供了潜在的分子基础。