Investigating the in vivo effect of Tribulus terrestris extract in middle cerebral artery occlusion rats using LC-MS-based metabolomics combined with molecular docking

被引:4
|
作者
Li, Xingxing [1 ,2 ]
Guo, Wenjun [2 ]
Zhao, Liang [1 ,2 ]
Xu, Dandan [2 ]
Xu, Xiaohang [2 ]
Han, Yuqing [2 ]
Wang, Chengyan [2 ]
Jiang, Yingzi [1 ,4 ]
Wang, Yang [3 ,5 ]
Xu, Yajuan [2 ]
机构
[1] Yanbian Univ, Sch Pharmaceut Sci, Yanji, Peoples R China
[2] Jilin Acad Chinese Med Sci, Key Lab Med Mat, Changchun, Peoples R China
[3] Changchun Univ Chinese Med, Jilin Ginseng Acad, Changchun, Peoples R China
[4] Yanbian Univ, Sch Pharmaceut Sci, Yanji 133002, Peoples R China
[5] Changchun Univ Chinese Med, Jilin Ginseng Acad, Changchun 130117, Peoples R China
关键词
metabolomics; middle cerebral artery occlusion; molecular docking; Tribulus terrestris extract; UHPLC-Q-Orbitrap MS; ISCHEMIC-STROKE; URIC-ACID; RISK; INJECTION;
D O I
10.1002/bmc.5614
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Tribulus terrestris L. fruit (TT) is a traditional Chinese herbal medicine used to treat ischemic stroke (IS). This study aimed to investigate the protective effect of TT extract, named TT15, on middle cerebral artery occlusion (MCAO) rats using metabolomics and molecular docking and find the targets of action and the material basis of TT15 against IS. The results of the infarct volume and neurological defect scores confirmed the efficacy of TT15. Serum metabolomics analysis using LC-MS revealed that model group animals experienced a variety of metabolic disturbances when compared to the sham group. TT15 can restore the MCAO-induced serum metabolite changes by modulating multiple metabolic pathways. Six enzymes were highlighted by the metabolite-reaction-enzyme-gene (M-R-E-G) network analysis, which might be the possible targets for the TT15 against IS. Molecular docking analysis was applied to show the binding affinities between active compounds and these enzymes. The representative docking mode with the lowest binding energy between three compounds and phospholipase A 2 (PLA2) and peroxidase (POD) was displayed by the ribbon binding map. This study profiles the metabolic changes in MCAO-induced IS and investigates the efficacy and the corresponding mechanism of TT15 in the treatment of IS.
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页数:11
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