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首页> 外文期刊>Scientific reports. >Herbal components of Japanese Kampo medicines exert laxative actions in colonic epithelium cells via activation of BK and CFTR channels
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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通道激活结肠上皮细胞中的泻药作用

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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 Ksup+/sup (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 Ksup+/sup 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是许多草药植物提取物的混合物,并通过刺激结肠上皮中的液体分泌来施加泻药作用。然而,这是未知这些粗康众药物的草药组分是有效的,刺激导致流体分泌的离子流出。在这里,我们选择了junchoto和mashiningan,mashinin(msn),kyonin(kyn),tonin(吨)和daio(dio)的四个草药组分,这是肝脏泻药,并检查了对人肠道的离子通道活性的影响上皮Caco-2细胞。贴片钳分析显示,MSN活化的囊性纤维化跨膜电导调节器(CFTR)通道的全电池电流特性,而Kyn,Ton和DIO活化大电导和电压激活的K + ( BK)频道。此外,电子电池尺寸表明,MSN诱导的分泌体积降低(SVD)对CFTR阻滞剂的敏感性,而TON,Kyn和DIO诱导对K + 通道阻挡器的SVD敏感性。总之,通过激活CFTR和BK通道,MSN和TON,KIN和DIO促进来自结肠上皮细胞的流体分泌。因此,日本Kampo药物,Juncho和Mashiningan,通过CFTR-和BK刺激草药组分的组合作用诱导KCl流出来发挥抗便秘作用。

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