基于 UPLC-Q-Exactive-MS 代谢组学和 HPLC-MS/MS 栀子苷组织分布的栀子豉汤肝毒性评价。

Evaluation of the Hepatotoxicity of the Zhi-Zi-Hou-Po Decoction by Combining UPLC-Q-Exactive-MS-Based Metabolomics and HPLC-MS/MS-Based Geniposide Tissue Distribution.

机构信息

Key Laboratory of Drug Quality Control and Pharmacovigilance, Ministry of Education, China Pharmaceutical University, Nanjing 210009, China.

Department of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing 210009, China.

出版信息

Molecules. 2019 Jan 31;24(3):511. doi: 10.3390/molecules24030511.

Abstract

With traditional Chinese medicine (TCM) becoming widespread globally, its safety has increasingly become a concern, especially its hepatoxicity. For example, Ellis is a key ingredient in the Zhi-Zi-Hou-Po decoction (ZZHPD), which is a commonly-used clinically combined prescription of TCM that may induce hepatoxicity. However, the underlying toxicity mechanism of ZZHPD is not fully understood. In this study, a plasma metabolomics strategy was used to investigate the mechanism of ZZHPD-induced hepatotoxicity through profiling entire endogenous metabolites. Twenty-four Sprague-Dawley rats were randomly assigned into four groups, which were orally administered with 0.9% saline, as well as 2.7 g/kg/day, 8.1 g/kg/day, or 27 g/kg/day of ZZHPD for 30 consecutive days, respectively. Biochemical assay and metabolomics assay were used to detect serum and plasma samples, whilst histopathological assay was used for detecting liver tissues, and the geniposide distribution in tissues was simultaneously measured. The results showed that the concentration of 20 metabolites linked to amino acid, lipid, and bile acid metabolism had significant changes in the ZZHPD-treated rats. Moreover, toxic effects were aggravated with serum biochemical and histopathological examines in liver tissues as the dosage increased, which may be associated with the accumulation of geniposide in the liver as the dosage increased. Notably, our findings also demonstrated that the combined metabolomics strategy with tissue distribution had significant potential for elucidating the mechanistic complexity of the toxicity of TCM.

摘要

随着中医药在全球范围内的广泛应用,其安全性越来越受到关注,尤其是其肝毒性。例如,栀子是栀子厚朴汤(ZZHPD)的主要成分之一,栀子厚朴汤是一种常用的临床联合中药处方,可能会引起肝毒性。然而,其潜在的毒性机制尚未完全阐明。在这项研究中,采用血浆代谢组学策略,通过分析整个内源性代谢物来研究 ZZHPD 诱导肝毒性的机制。将 24 只 Sprague-Dawley 大鼠随机分为四组,分别灌胃给予 0.9%生理盐水、2.7 g/kg/d、8.1 g/kg/d 或 27 g/kg/d 的 ZZHPD,连续 30 天。采用生化检测和代谢组学检测血清和血浆样本,同时进行组织病理学检测肝脏组织,并同时检测组织中京尼平苷的分布。结果表明,20 种与氨基酸、脂质和胆汁酸代谢相关的代谢物的浓度在 ZZHPD 处理的大鼠中发生了显著变化。此外,随着血清生化和组织病理学检查显示肝组织损伤的加重,毒性作用也随之加重,这可能与京尼平苷在肝脏中的积累有关。值得注意的是,我们的研究结果还表明,结合组织分布的代谢组学策略具有阐明中药毒性机制复杂性的巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b30/6384998/1c16f2577056/molecules-24-00511-g001.jpg

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