The Experimental Research Center, College of Pharmacy, Anhui University of Chinese Medicine, Hefei 230038, China; Key Laboratory of Chinese Medicinal Formula of Anhui Province, Hefei 230038, China.
Key Laboratory of Chinese Medicinal Formula of Anhui Province, Hefei 230038, China.
J Pharm Biomed Anal. 2019 Feb 5;164:187-195. doi: 10.1016/j.jpba.2018.10.041. Epub 2018 Oct 28.
The direct cause of hepatolenticular degeneration (HLD) is copper metabolic disorder caused by autosomal recessive inheritance. Gandou decoction (GDD), a classical traditional Chinese medicine formula, exhibits unambiguous therapeutic effect on HLD in China for decades. However, the mechanism of effect on HLD is not clear. With this purpose, the effects of copper content and histopathology inspection on the HLD rat model were investigated. Then, metabolomics study based on ultra-performance liquid chromatography quadrupole-time-of-flight mass spectrometry (UPLC-Q-TOF/MS) analysis and multivariate statistical analysis was adopted to further reveal the mechanism of action of GDD against HLD. The results showed that the characteristics of liver tissues after GDD treatment were significantly reversed, close to the control group, suggesting that GDD has a therapeutic effect on HLD. Furthermore, HLD interferes with 2 metabolites of the metabolic pathway in rats. Among them, up-regulation of Lactic acid, Tryptophan, Phenylalanine, Triacylglycerol and down-regulation of Linoleic acid, Alpha Linolenic acid, Phosphatidylcholine, Taurine is particularly significant. Analysis of metabolic pathways by a unique pathway analysis revealed significant changes in several pathways including lipid metabolism, amino metabolism and glucose metabolism in HLD. This study showed that GDD could provide satisfactory therapeutic effects on HLD and metabolomics study can be utilized to further understand the molecular mechanisms.
肝豆状核变性(HLD)的直接病因是常染色体隐性遗传所致的铜代谢障碍。肝豆汤(GDD)是一种经典的中药方剂,在中国治疗 HLD 已有几十年的历史,疗效确切。但其作用机制尚不清楚。本研究以铜含量和组织病理学检查为切入点,观察 GDD 对 HLD 大鼠模型的影响,采用基于超高效液相色谱四极杆飞行时间质谱联用(UPLC-Q-TOF/MS)分析的代谢组学研究和多元统计分析方法,进一步揭示 GDD 抗 HLD 的作用机制。结果表明,GDD 治疗后大鼠肝脏组织的特征明显逆转,接近对照组,提示 GDD 对 HLD 有治疗作用。此外,HLD 干扰了大鼠代谢途径中的 2 种代谢物。其中,乳酸、色氨酸、苯丙氨酸、甘油三酯上调,亚油酸、α-亚麻酸、磷脂酰胆碱、牛磺酸下调尤为显著。通过独特的途径分析对代谢途径进行分析,发现 HLD 中脂质代谢、氨基酸代谢和糖代谢等几个途径发生了显著变化。本研究表明,GDD 可对 HLD 提供满意的治疗效果,代谢组学研究可进一步深入了解其分子机制。