Plasma Metabolomic Profiling to Reveal Antipyretic Mechanism of Shuang-Huang-Lian Injection on Yeast-Induced Pyrexia Rats

被引:37
作者
Gao, Xiaoyan [1 ]
Guo, Mingxing [1 ]
Li, Qiang [2 ]
Peng, Long [1 ]
Liu, Haiyu [1 ]
Zhang, Li [1 ]
Bai, Xu [3 ]
Wang, Yingxin [4 ]
Li, Jian [5 ]
Cai, Chengke [2 ]
机构
[1] Beijing Univ Chinese Med, Sci Expt Ctr TCM, Beijing, Peoples R China
[2] Beijing Univ Chinese Med, Sch Chinese Mat Med, Beijing, Peoples R China
[3] Waters Technol Shanghai Ltd, Shanghai, Peoples R China
[4] 2nd Tradit Chinese Med Factory Harbin Pharm Grp C, Harbin, Peoples R China
[5] Beijing Univ Chinese Med, Sch Basic Med Sci, Beijing, Peoples R China
来源
PLOS ONE | 2014年 / 9卷 / 06期
基金
美国国家科学基金会;
关键词
BETA-HYDROXYBUTYRIC ACID; DISEASE DIAGNOSIS; MASS-SPECTROMETRY; BAKERS-YEAST; METABONOMICS; FEVER; FAD; FMN; IDENTIFICATION; EXPRESSION;
D O I
10.1371/journal.pone.0100017
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Shuang-huang-lian injection (SHLI) is a famous Chinese patent medicine, which has been wildly used in clinic for the treatment of acute respiratory tract infection, pneumonia, influenza, etc. The existing randomized controlled trial (RCT) studies suggested that SHLI could afford a certain anti-febrile action. However, seldom does research concern the pharmacological mechanisms of SHLI. In the current study, we explored plasma metabolomic profiling technique and selected potential metabolic markers to reveal the antipyretic mechanism of SHLI on yeast-induced pyrexia rat model using UPLC-Q-TOF/MS coupled with multivariate statistical analysis and pattern recognition techniques. We discovered a significant perturbance of metabolic profile in the plasma of fever rats and obvious reversion in SHLI-administered rats. Eight potential biomarkers, i.e. 1) 3-hydeoxybutyric acid, 2) leucine, 3) 16:0 LPC, 4) allocholic acid, 5) vitamin B2, 6) Cys-Lys-His, 7) 18:2 LPC, and 8) 3-hydroxychola-7, 22-dien-24-oic acid, were screened out by OPLS-DA approach. Five potential perturbed metabolic pathways, i.e. 1) valine, leucine, and isoleucine biosynthesis, 2) glycerophospholipid metabolism, 3) ketone bodies synthesis and degradation, 4) bile acid biosynthesis, and 5) riboflavin metabolism, were revealed to relate to the antipyretic mechanisms of SHLI. Overall, we investigated antipyretic mechanisms of SHLI at metabolomic level for the first time, and the obtained results highlights the necessity of adopting metabolomics as a reliable tool for understanding the holism and synergism of Chinese patent drug.
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页数:10
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