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Herbal components of Japanese Kampo medicines exert laxative actions in colonic epithelium cells via activation of BK and CFTR channels

机译:日本Kampo药物的草药成分通过激活BK和CFTR通道在结肠上皮细胞中发挥通便作用

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摘要

Japanese Kampo medicines Junchoto and Mashiningan are mixtures of numerous herbal plant extracts and empirically known to exert laxative actions by stimulating fluid secretion in the colonic epithelium. However, it is unknown which and how the herbal components of these crude Kampo drugs are effective to stimulate ion effluxes causing fluid secretion. Here, we selected four herbal components of Junchoto and Mashiningan, Mashinin (MSN), Kyonin (KYN), Tonin (TON), and Daio (DIO), which are putatively laxatives, and examined their effects on the ion channel activity of human colonic epithelial Caco-2 cells. Patch clamp analyses revealed that MSN activated whole-cell current characteristics of the cystic fibrosis transmembrane conductance regulator (CFTR) channel, whereas KYN, TON, and DIO activated the large-conductance and voltage-activated K+ (BK) channel. Furthermore, electronic cell sizing showed that MSN induced secretory volume decrease (SVD) sensitivity to a CFTR blocker, whereas TON, KYN, and DIO induced SVD sensitivity to a K+ channel blocker. In conclusion, MSN and TON, KYN, and DIO promote fluid secretion from colonic epithelial cells by activating CFTR and BK channels. Thus, Japanese Kampo medicines, Junchoto and Mashiningan, exert anti-constipation actions by inducing KCl efflux through the combined actions of CFTR- and BK-stimulating herbal components.
机译:日本Kampo药物Junchoto和Mashiningan是多种草药植物提取物的混合物,根据经验已知可通过刺激结肠上皮中的液体分泌发挥通便作用。但是,尚不清楚这些粗制坎普药物中的哪些草药成分以及如何有效刺激引起液体分泌的离子流出。在这里,我们选择了Junchoto和Mashiningan的四种草药成分,Mashinin(MSN),Kyonin(KYN),Tonin(TON)和Daio(DIO)(假定是泻药),并研究了它们对人结肠离子通道活性的影响。上皮Caco-2细胞。膜片钳分析显示,MSN激活了囊性纤维化跨膜电导调节器(CFTR)通道的全细胞电流特性,而KYN,TON和DIO激活了大电导和电压激活的K + ( BK)频道。此外,电子细胞大小测定表明,MSN诱导的对CFTR阻断剂的分泌量减少(SVD)敏感性,而TON,KYN和DIO诱导的SVD对K + 通道阻断剂的敏感性。总之,MSN和TON,KYN和DIO通过激活CFTR和BK通道来促进结肠上皮细胞的液体分泌。因此,日本Kampo药品Junchoto和Mashiningan通过CFTR和BK刺激性草药成分的联合作用诱导KCl外排,从而发挥抗便秘作用。

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