Liao Wenting, Jin Qiwen, Liu Junning, Ruan Yiling, Li Xinran, Shen Yueyue, Zhang Zhicheng, Wang Yong, Wu Shengming, Zhang Junying, Kang Lifeng, Wu Chunyong
Department of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing, China.
Institute of Forensic Science, Nanjing Municipal Public Security Bureau, Nanjing, China.
Front Pharmacol. 2021 Mar 29;12:599180. doi: 10.3389/fphar.2021.599180. eCollection 2021.
Acute liver failure (ALF) is a serious clinical disorder with high fatality rates. Mahuang decoction (MHD), a well-known traditional Chinese medicine, has multiple pharmacological effects, such as anti-inflammation, anti-allergy, anti-asthma, and anti-hyperglycemia. In this study, we investigated the protective effect of MHD against ALF. In the lipopolysaccharide and D-galactosamine (LPS/D-GalN)-induced ALF mouse model, the elevated activities of the serum alanine and aspartate transaminases as well as the liver pathological damage were markedly alleviated by MHD. Subsequently, a metabolomics study based on the ultrahigh performance liquid chromatograph coupled with Q Exactive Orbitrap mass spectrometry was carried to clarify the therapeutic mechanisms of MHD against ALF. A total of 36 metabolites contributing to LPS/D-GalN-induced ALF were identified in the serum samples, among which the abnormalities of 27 metabolites were ameliorated by MHD. The analysis of metabolic pathways revealed that the therapeutic effects of MHD are likely due to the modulation of the metabolic disorders of tricarboxylic acid (TCA) cycle, retinol metabolism, tryptophan metabolism, arginine and proline metabolism, nicotinate and nicotinamide metabolism, phenylalanine metabolism, phenylalanine, tyrosine and tryptophan synthesis, as well as cysteine and methionine metabolism. This study demonstrated for the first time that MHD exerted an obvious protective effect against ALF mainly through the regulation of TCA cycle and amino acid metabolism, highlighting the importance of metabolomics to investigate the drug-targeted metabolic pathways.
急性肝衰竭(ALF)是一种死亡率很高的严重临床病症。麻黄汤(MHD)是一种著名的传统中药,具有多种药理作用,如抗炎、抗过敏、抗哮喘和抗高血糖。在本研究中,我们研究了MHD对ALF的保护作用。在脂多糖和D-半乳糖胺(LPS/D-GalN)诱导的ALF小鼠模型中,MHD显著减轻了血清丙氨酸和天冬氨酸转氨酶活性的升高以及肝脏病理损伤。随后,进行了一项基于超高效液相色谱与Q Exactive Orbitrap质谱联用的代谢组学研究,以阐明MHD对ALF的治疗机制。在血清样本中总共鉴定出36种导致LPS/D-GalN诱导的ALF的代谢物,其中27种代谢物的异常被MHD改善。代谢途径分析表明,MHD的治疗作用可能是由于对三羧酸(TCA)循环、视黄醇代谢、色氨酸代谢、精氨酸和脯氨酸代谢、烟酸和烟酰胺代谢、苯丙氨酸代谢、苯丙氨酸、酪氨酸和色氨酸合成以及半胱氨酸和甲硫氨酸代谢的代谢紊乱的调节。本研究首次证明MHD主要通过调节TCA循环和氨基酸代谢对ALF发挥明显的保护作用,突出了代谢组学在研究药物靶向代谢途径方面的重要性。