Investigation of the hepatoprotective effect of Corydalis saxicola Bunting on carbon tetrachloride-induced liver fibrosis in rats by 1H-NMR-based metabonomics and network pharmacology approaches

被引:40
|
作者
Liu, Xu-Wen [1 ]
Tang, Chao-Ling [1 ,2 ]
Zheng, Hua [3 ]
Wu, Jin-Xia [1 ]
Wu, Fang [1 ]
Mo, Yi-Yi [1 ]
Liu, Xi [1 ]
Zhu, Hong-Jia [1 ]
Yin, Chun-Li [1 ]
Cheng, Bang [1 ]
Ruan, Jun-Xiang [1 ]
Song, Fang-Ming [1 ]
Chen, Zhao-Ni [1 ]
Song, Hui [1 ]
Guo, Hong-Wei [1 ]
Liang, Yong-Hong [1 ]
Su, Zhi-Heng [1 ]
机构
[1] Guangxi Med Univ, Pharmaceut Coll, Nanning 530021, Peoples R China
[2] Hainan Med Coll, Affiliated Hosp 1, Dept Pharm, Haikou 571000, Hainan, Peoples R China
[3] Guangxi Med Univ, Life Sci Inst, Nanning 530021, Peoples R China
关键词
Corydalis saxicola bunting; Liver fibrosis; Metabonomics(1)H-NMR; Network pharmacology; Carbon tetrachloride; CHAIN AMINO-ACIDS; HEPATOTOXICITY; ALKALOIDS; EXPRESSION; CIRRHOSIS; DISEASE; CELLS; MICE;
D O I
10.1016/j.jpba.2018.06.065
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Liver fibrosis is a common consequence of chronic liver diseases resulting from multiple etiologies. Furthermore, prolonged unresolved liver fibrosis may gradually progress to cirrhosis, and eventually evolve into hepatocellular carcinoma (HCC). Corydalis saxicola Bunting (CS), a type of traditional Chinese folk medicine, has been reported to have hepatoprotective effects on the liver. However, the exact mechanism of how it cures liver fibrosis requires further elucidation. In this work, an integrated approach combining proton nuclear magnetic resonance (1 H-NMR)-based metabonomics and network pharmacology was adopted to elucidate the anti-fibrosis mechanism of CS. Metabonomic study of serum biochemical changes by carbon tetrachloride (CCI4)-induced liver fibrosis in rats after CS treatment were performed using IFI-NMR analysis. Metabolic profiling by means of partial least squares-discriminate analysis (PLSDA) indicated that the metabolic perturbation caused by CC14 was reduced after CS treatment. As a result, lipids, leucine, alanine, acetate, O-acetyl-glycoprotein and creatine were significantly restored after CS treatment, which regulated valine, leucine and isoleucine metabolism; arginine and proline metabolism; lipid metabolism and pyruvate metabolism. Additionally, 157 potential targets of CS and 265 targets of liver fibrosis were identified by means of network pharmacology. Subsequently, 5 target proteins, which are the intersection of potential CS targets and liver fibrosis targets, indicated that CS has potential anti-fibrosis effects through regulating alanine aminotransferase (ALT) activity, the farnesoid X receptor (FXR), cyclooxygenase-2 (COX-2), matrix metalloproteinase-1 (MMP-1) and angiotensinogen. Chelerythrine and sanguinarine were the potential active compounds in CS for treating liver fibrosis through regulating ALT activity. This study is the first report to study the anti-fibrosis effects of CS on the basis of combining a metabonomics and network pharmacology approaches, and it may be a potentially powerful tool to study the efficacy and mechanisms of traditional Chinese folk medicines. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:252 / 261
页数:10
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