Zhou Wenwen, Zhang Xiaoxiao, Liu Meijuan, Wan Meiyu, Jiang Shu, Shang Erxin, Duan Jinao
Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, Nanjing University of Chinese Medicine, 138 Xianlin Road, Nanjing 210023, PR China.
Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, Nanjing University of Chinese Medicine, 138 Xianlin Road, Nanjing 210023, PR China.
J Pharm Biomed Anal. 2025 Nov 15;265:117066. doi: 10.1016/j.jpba.2025.117066. Epub 2025 Jul 15.
Guishao Yigong Decoction (GYD), a classic prescription that tonifies the spleen and qi, has been used in clinical practices for thousands of years to treat spleen deficiency. However, its in vitro and in vivo metabolic characteristics are still unclear. In this study, a rapid and reliable analytical method based on ultra-high-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF/MS) with automated data processing (MetaboLynx) was established to investigate the metabolites and metabolic pathways of GYD in vivo and in vitro. Based on the characteristics of protonated ions, eleven precursors (ginsenoside Re, ginsenoside Rg1, ginsenoside Rb1, atractylenolide I, atractylenolide III, paeoniflorin, glycyrrhizic acid, pachymic acid, liquiritin, nobiletin, and ferulic acid) and their corresponding metabolites were detected and tentatively identified. A total of 81 metabolites were identified, including 53 metabolites in vivo, 40 metabolites of liver microsomes, and 43 metabolites of intestinal flora in vitro. Distinct metabolic patterns were observed between intestinal flora and liver microsomes - the former primarily catalyzed phase I transformations (hydroxylation, methylation, dehydroxylation, demethylation, and reduction), while the latter also executed phase II metabolism, with glucuronidation being the predominant conjugation reaction. The metabolic profiling and pathways of active components in GYD were systematically analyzed, which was helpful in clarifying its potential mechanism and clinical application.
归芍异功汤(GYD)是一种经典的健脾益气方剂,数千年来一直用于临床治疗脾虚证。然而,其体内外代谢特征仍不清楚。本研究建立了一种基于超高效液相色谱-四极杆飞行时间质谱联用(UPLC-Q-TOF/MS)和自动数据处理(MetaboLynx)的快速可靠分析方法,以研究GYD在体内外的代谢产物和代谢途径。根据质子化离子的特征,检测并初步鉴定了11种前体(人参皂苷Re、人参皂苷Rg1、人参皂苷Rb1、白术内酯I、白术内酯III、芍药苷、甘草酸、茯苓酸、甘草苷、川陈皮素和阿魏酸)及其相应代谢产物。共鉴定出81种代谢产物,包括53种体内代谢产物、40种肝微粒体代谢产物和43种体外肠道菌群代谢产物。肠道菌群和肝微粒体之间观察到明显的代谢模式差异——前者主要催化I相转化(羟基化、甲基化、脱羟基化、去甲基化和还原),而后者也进行II相代谢,其中葡萄糖醛酸化是主要的结合反应。系统分析了GYD中活性成分的代谢谱和代谢途径,有助于阐明其潜在机制和临床应用。