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全面代谢组学分析 inchinkoto 的药理作用,一种具有保肝作用的草药。

Comprehensive metabolome analysis for the pharmacological action of inchinkoto, a hepatoprotective herbal medicine.

机构信息

Division of Surgical Oncology, Department of Surgery, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan.

Tsumura Advanced Technology Research Laboratories, Tsumura & CO., Ibaraki, Japan.

出版信息

Metabolomics. 2021 Dec 2;17(12):106. doi: 10.1007/s11306-021-01824-0.

Abstract

INTRODUCTION

The precise pharmacological action of inchinkoto (ICKT, Yin-Chen-Hao-Tang in Chinese), a hepatoprotective herbal medicine, on total metabolic pathways has not been well investigated.

OBJECTIVES

The aim of this study was to explore the serum metabolites reflecting the pharmacological activity of ICKT, and mechanism of action of ICKT using serum metabolome analysis.

METHODS

54 patients with obstructive jaundice due to malignancies were included in this study. ICKT was administered for 3 days. Serum and bile samples were collected before and 1 h after ICKT administration on days 1 and 4. Serum metabolome analysis including ICKT components were performed.

RESULTS

The levels of total/direct bilirubin, C-reactive protein, γ-glutamyl transpeptidase, and albumin in the serum were significantly improved after ICKT administration. In the serum metabolome analysis, inosine was the only elevated metabolite on days 1 and 4. Most of the metabolites which were significantly changed after ICKT administration were lipid mediators, and all decreased on day 1. Notably, the levels of many lipid mediators were increased on day 4. The difference in serum aspartic acid 1 h after ICKT administration was significantly correlated with a decrease in the levels of total bilirubin in the serum on day 4.

CONCLUSIONS

Using metabolome analysis, we demonstrated several metabolic changes that may be associated with the pharmacological mechanisms of ICKT. The biological implications of these metabolites should be further investigated in basic research studies.

摘要

简介

茵陈蒿汤(ICKT,中药茵陈蒿汤)作为一种保肝草药,其确切的药理作用对总代谢途径尚未得到很好的研究。

目的

本研究旨在通过血清代谢组学分析探讨反映 ICKT 药理活性及作用机制的血清代谢物。

方法

本研究纳入了 54 例因恶性肿瘤引起的阻塞性黄疸患者。ICKT 给药 3 天。分别于给药第 1 天和第 4 天的第 1 天和第 1 天采集血清和胆汁样本。进行包括 ICKT 成分在内的血清代谢组学分析。

结果

ICKT 给药后血清总/直接胆红素、C 反应蛋白、γ-谷氨酰转肽酶和白蛋白水平明显改善。在血清代谢组学分析中,肌苷是第 1 天和第 4 天唯一升高的代谢物。大多数给药后明显变化的代谢物是脂质介质,所有这些代谢物在第 1 天均减少。值得注意的是,许多脂质介质的水平在第 4 天增加。ICKT 给药后 1 小时血清天冬氨酸的差异与第 4 天血清总胆红素水平的降低显著相关。

结论

通过代谢组学分析,我们证明了几种可能与 ICKT 药理机制相关的代谢变化。这些代谢物的生物学意义应在基础研究中进一步研究。

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