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

• Published in: Scientific reports Vol. 9; no. 1; pp. 15554 - 9
• Main Authors: Numata, Tomohiro, Sato-Numata, Kaori, Okada, Yasunobu
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 29.10.2019; Nature Publishing Group
• Subjects: 631/80; 692/4020; 9/74; Caco-2 Cells; Cell activation; Channel gating; Colon; Colon - metabolism; Constipation; Cystic fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator - metabolism; Epithelial cells; Epithelium; HEK293 Cells; Humanities and Social Sciences; Humans; Intestinal Mucosa - metabolism; Large-Conductance Calcium-Activated Potassium Channels - metabolism; Laxatives; Laxatives - chemistry; Laxatives - pharmacology; Medicinal plants; Medicine, Kampo; multidisciplinary; Plant extracts; Plants, Medicinal - chemistry; Potassium channels; Potassium channels (calcium-gated); Potassium channels (voltage-gated); Potassium chloride; Potassium conductance; Science; Science (multidisciplinary); Secretion
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-019-52171-z

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.