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Inhibition of Ca <sup>2+</sup> ‐activated Cl <sup>−</sup> channels by gallotannins as a possible molecular basis for health benefits of red wine and green tea

W. NamkungDepartments of Medicine and Physiology University of California San Francisco California USAJay R. ThiagarajahDepartments of Medicine and Physiology University of California San Francisco California USAPuay‐Wah PhuanDepartments of Medicine and Physiology University of California San Francisco California USAA.S. VerkmanDepartments of Medicine and Physiology University of California San Francisco California USA
2010en
ABI

Аннотация

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.

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