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采用超高效液相色谱/四极杆飞行时间质谱法鉴定2型糖尿病大鼠口服交泰丸后血浆中的成分及代谢产物。

Identification of components and metabolites in plasma of type 2 diabetic rat after oral administration of Jiao-Tai-Wan using ultra-performance liquid chromatography/quadrupole time-of-flight mass spectrometry.

作者信息

Li Zhihui, Chen Jianhua, Gao Xing, Zhang Ting, Zheng Wei, Wei Guijie, Huang Yunfang, Qi Jing, Zhang Yujie, Ma Pengkai

机构信息

School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, P. R. China.

出版信息

J Sep Sci. 2020 Jul;43(13):2690-2707. doi: 10.1002/jssc.201901040. Epub 2020 May 5.

Abstract

Jiao-Tai-Wan, which is composed of Coptis Rhizoma and Cinnamon Cortex, has been recently used to treat type 2 diabetes. Owing to lack of data on its prototypes and metabolites, elucidation of the pharmacological and clinically safe levels of this formula has been significantly hindered. To screen more potential bioactive components of Jiao-Tai-Wan, we identified its multiple prototypes and metabolites in the plasma of type 2 diabetic rats by ultra high performance liquid chromatography/quadrupole-time-of-flight mass spectrometry. A total of 47 compounds were identified in the plasma of type 2 diabetic rats, including 22 prototypes and 25 metabolites, with alkaloids constituting the majority of the absorbed prototype components. In addition, this is the first study to detect vanillic acid, gallic acid, chlorogenic acid, protocatechuic acid, 2-hydroxycinnamic acid, 3-hydroxycinnamic acid, 4-hydroxycinnamic acid, and 2-methoxy cinnamic acid after oral administration of Jiao-Tai-Wan. The prototypes from Jiao-Tai-Wan were extensively metabolized by demethylation, hydroxylation, and reduction in phase Ⅰ metabolic reactions and by methylation or conjugation of glucuronide or sulfate in phase Ⅱ reactions. This is the first systematic study on the components and metabolic profiles of Jiao-Tai-Wan in vivo. This study provides a useful chemical basis for further pharmacological research and clinical application of Jiao-Tai-Wan.

摘要

交泰丸由黄连和肉桂组成,最近被用于治疗2型糖尿病。由于缺乏其原型和代谢物的数据,该方剂的药理作用及临床安全剂量的阐明受到了显著阻碍。为了筛选交泰丸更多潜在的生物活性成分,我们通过超高效液相色谱/四极杆-飞行时间质谱法鉴定了2型糖尿病大鼠血浆中的多种原型和代谢物。在2型糖尿病大鼠血浆中总共鉴定出47种化合物,包括22种原型和25种代谢物,其中生物碱是吸收的原型成分中的主要部分。此外,这是首次在口服交泰丸后检测到香草酸、没食子酸、绿原酸、原儿茶酸、2-羟基肉桂酸、3-羟基肉桂酸、4-羟基肉桂酸和2-甲氧基肉桂酸的研究。交泰丸的原型在Ⅰ相代谢反应中通过去甲基化、羟基化和还原进行广泛代谢,在Ⅱ相反应中通过甲基化或与葡萄糖醛酸或硫酸盐结合进行代谢。这是首次对交泰丸体内成分和代谢谱进行的系统研究。本研究为交泰丸进一步的药理研究和临床应用提供了有用的化学依据。

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