Investigating the mechanisms of Modified Xiaoyaosan (tiaogan-liqi prescription) in suppressing the progression of atherosclerosis, by means of integrative pharmacology and experimental validation

被引:7
作者
Chen, Mingtai [1 ,2 ,3 ]
Luo, Yong [4 ]
Men, Ling [5 ]
Lin, Bo [6 ]
Lin, Haidan [1 ]
Li, Ying [1 ]
Zhong, Guofu [6 ]
Zhong, Xiaoling [7 ]
Fu, Wenjun [4 ]
Zhou, Hua [2 ,3 ]
Tong, Guangdong [2 ,3 ,8 ]
Liu, Qiang [1 ]
Luan, Jienan [1 ]
机构
[1] Shenzhen Tradit Chinese Med Hosp, Dept Cardiovasc Dis, Shenzhen, Peoples R China
[2] Macau Univ Sci & Technol, Fac Chinese Med, Macau, Peoples R China
[3] Macau Univ Sci & Technol, State Key Lab Qual Res Chinese Med, Macau, Peoples R China
[4] Guangzhou Univ Chinese Med, Sch Basic Med Sci, Ctr Integrat Med, Guangzhou, Guangdong, Peoples R China
[5] Shenzhen Tradit Chinese Med Hosp, Nephrol Dept, Shenzhen, Peoples R China
[6] Shenzhen Tradit Chinese Med Hosp, Intens Care Unit, Shenzhen, Peoples R China
[7] Shenzhen Tradit Chinese Med Hosp, Reprod Hlth Dept, Shenzhen, Peoples R China
[8] Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Dept Liver Dis, Shenzhen, Peoples R China
来源
AGING-US | 2021年 / 13卷 / 08期
关键词
atherosclerosis; traditional Chinese medicine; Modified Xiaoyaosan prescription; integrative pharmacology; network analysis; INHIBITION; CYTOKINES; DISEASE; PROTEIN; ATORVASTATIN; DECREASES;
D O I
10.18632/aging.202832
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Atherosclerosis (AS)-related diseases remain among the leading causes of death worldwide. Modified Xiaoyaosan (also called Tiaogan-Liqi prescription, TGLQ), a traditional Chinese medical formulation, has been widely applied in the treatment of AS-related diseases. The aim of this study was to investigate the underlying pharmacological mechanisms of TGLQ in acting on AS. A total of 548 chemical compounds contained in TGLQ, and 969 putative targets, were collected from the Computation Platform for Integrative Pharmacology of Traditional Chinese Medicine, while 1005 therapeutic targets for the treatment of AS were obtained from the DisGeNET, TTD and CTD databases. Moreover, the 63 key targets were screened by the intersection of the targets above, and by network topological analysis. Further functional enrichment analysis showed that the key targets were significantly associated with regulation of the immune system and inflammation, improvement of lipid and glucose metabolism, regulation of the neuroendocrine system and anti-thrombosis effect. The in vivo experiments confirmed that TGLQ could reduce plasma lipid profiles and plasma inflammatory cytokines, and also inhibit AS plaque formation, within the AS model ApoE-/- mice. The in vitro experiments validated the hypothesis that TGLQ could significantly reduce intracellular lipid accumulation, suppress the production of inflammatory cytokines of macrophages induced by oxidized-LDL, and inhibit the protein expression of heat shock protein 90 and toll-like receptor 4. This study identified a list of key targets of TGLQ in the treatment of AS by applying an integrative pharmacology approach, which was validated by in vivo and in vitro experimentation.
引用
收藏
页码:11411 / 11432
页数:22
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