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通过药物微生物组学预测恶性肿瘤相关梗阻性黄疸患者 Inchinkoto 的疗效。

Predicting Inchinkoto efficacy, in patients with obstructive jaundice associated with malignant tumors, through pharmacomicrobiomics.

机构信息

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.

出版信息

Pharmacol Res. 2022 Jan;175:105981. doi: 10.1016/j.phrs.2021.105981. Epub 2021 Nov 17.

Abstract

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.

摘要

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。

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