Li Haojie, Cao Wenli, Lu Mengxi, Wu Chunxiao, Wang Xinguo, Niu Liying
Shijiazhuang Hospital of Traditional Chinese Medicine, Shijiazhuang, Hebei 050051, China.
Hebei TCM Formula Granule Engineering & Technology Research Center, Hebei University of Chinese Medicine, Shijiazhuang, Hebei 050200, China.
Evid Based Complement Alternat Med. 2017;2017:9038260. doi: 10.1155/2017/9038260. Epub 2017 Dec 11.
Total glucosides of paeony (TGP) have been confirmed to be hepatoprotective. However, the underlying mechanism is largely unclear. In this study, we investigated the metabolic profiles of urine and serum in rats with carbon tetrachloride- (CCl-) induced experimental liver injury and TGP administration by using ultra-performance liquid chromatography-mass spectrometry (UPLC-MS). The vehicle or a single dose of TGP was intragastrically administered to Wistar rats once a day for 14 consecutive days. To induce ALI, 50% CCl was injected intraperitoneally into these rats 2 hours after the last time administration of saline of TGP at the 14th day. The results indicated that TGP administration could protect rats from CCl-induced ALI and alanine aminotransferase (ALT) and aspartate aminotransferase (AST) elevation, as well as hepatocyte apoptosis and inflammation. Furthermore, metabolomics analysis showed that TGP treatment significantly attenuated CCl-triggered deregulation of multiple metabolites in both urine and serum, including glycine, alanine, proline, and glutamine. Metabolite set enrichment and pathway analyses demonstrated that amino acid cycling and glutathione metabolism were two main pathways involved in CCl-induced experimental liver injury and TGP administration. Taken together, these findings revealed that regulation of metabolites potentially plays a pivotal role in the protective effect of TGP on ALI.
芍药总苷(TGP)已被证实具有肝脏保护作用。然而,其潜在机制尚不清楚。在本研究中,我们通过超高效液相色谱 - 质谱联用技术(UPLC-MS)研究了四氯化碳(CCl)诱导的实验性肝损伤大鼠及给予TGP后的尿液和血清代谢谱。将溶媒或单剂量的TGP每日一次灌胃给予Wistar大鼠,连续14天。在第14天最后一次给予生理盐水或TGP 2小时后,腹腔注射50% CCl以诱导急性肝损伤(ALI)。结果表明,给予TGP可保护大鼠免受CCl诱导的ALI以及丙氨酸氨基转移酶(ALT)和天冬氨酸氨基转移酶(AST)升高,以及肝细胞凋亡和炎症。此外,代谢组学分析表明,TGP治疗显著减轻了CCl引发的尿液和血清中多种代谢物的失调,包括甘氨酸、丙氨酸、脯氨酸和谷氨酰胺。代谢物集富集和通路分析表明,氨基酸循环和谷胱甘肽代谢是CCl诱导的实验性肝损伤及给予TGP过程中涉及的两个主要通路。综上所述,这些发现揭示了代谢物的调节可能在TGP对ALI的保护作用中起关键作用。