Division of Surgical Oncology, Department of Surgery, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
Tsumura Advanced Technology Research Laboratories, Tsumura & Co., Ami-machi, Ibaraki, Japan.
Pharmacol Res. 2022 Jan;175:105981. doi: 10.1016/j.phrs.2021.105981. Epub 2021 Nov 17.
Inchinkoto (ICKT) is a popular choleretic and hepatoprotective herbal medicine that is widely used in Japan. Geniposide, a major ingredient of ICKT, is metabolized to genipin by gut microbiota, which exerts a choleretic effect. This study investigates the relationship between stool genipin-producing activity and diversity of the clinical effect of ICKT in patients with malignant obstructive jaundice. Fifty-two patients with malignant obstructive jaundice who underwent external biliary drainage were included. ICKT was administered as three packets per day (7.5 g/day) for three days and 2.5 g on the morning of the fourth day. Stool samples were collected before ICKT administration and bile flow was monitored on a daily basis. The microbiome, genipin-producing activity, and organic acids in stools were analyzed. The Shannon-Wiener (SW) index was calculated to evaluate gut microbiome diversity. The stool genipin-producing activity showed a significant positive correlation with the SW index. Stool genipin-producing activity positively correlated with the order Clostridia (obligate anaerobes), but negatively correlated with the order Lactobacillales (facultative anaerobes). Moreover, stool genipin-producing activity was positively correlated to the concentration valeric acid, but negatively correlated to the concentration of lactic acid and succinic acid. The change of bile flow at 2 and 3 days after ICKT administration showed significant positive correlation with genipin-producing activity (correlation coefficient, 0.40 and 0.29, respectively, P < 0.05). An analysis of stool profile, including stool genipin-producing activity, may predict the efficacy of ICKT. Modification of the microbiome may be a target to enhance the therapeutic effect of ICKT.
茵陈蒿汤(ICKT)是一种流行的利胆和保肝草药,在日本被广泛使用。其主要成分之一京尼平苷经肠道菌群代谢为京尼平,发挥利胆作用。本研究旨在探讨恶性梗阻性黄疸患者ICKT 临床疗效与粪便中产京尼平酶活性及菌群多样性的关系。52 例接受外引流术的恶性梗阻性黄疸患者入组,ICKT 治疗方案为:连续 3 天,每天 3 包(7.5 g/包),第 4 天早上 2.5 g。治疗前和治疗期间每天采集粪便样本,监测胆汁流量。分析肠道微生物群、粪便中产京尼平酶活性和有机酸。采用 Shannon-Wiener(SW)指数评估肠道微生物多样性。粪便中产京尼平酶活性与 SW 指数呈显著正相关。粪便中产京尼平酶活性与厚壁菌门(专性厌氧菌)呈正相关,与乳杆菌门(兼性厌氧菌)呈负相关。此外,粪便中产京尼平酶活性与戊酸浓度呈正相关,与乳酸和琥珀酸浓度呈负相关。ICKT 给药后 2 天和 3 天胆汁流量的变化与产京尼平酶活性呈显著正相关(相关系数分别为 0.40 和 0.29,P 均<0.05)。分析粪便特征,包括粪便中产京尼平酶活性,可能预测 ICKT 的疗效。菌群的改变可能是增强 ICKT 治疗效果的靶点。