Buyang Huanwu Decoction ameliorates ischemic stroke by modulating multiple targets with multiple components: In vitro evidences

被引:32
作者
Zhang Wei-Wei [1 ,2 ]
Xu Feng [3 ]
Wang Ding [1 ]
Ye Jia [1 ]
Cai Shao-Qing [3 ]
机构
[1] Peking Univ, Sch Pharmaceut Sci, Dept Mol & Cellular Pharmacol, Beijing 100191, Peoples R China
[2] Tsinghua Univ, Beijing Tsinghua Changgung Hosp Med Ctr, Dept Clin Pharm, Beijing 102218, Peoples R China
[3] Peking Univ, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
Buyang Huanwu Decoction; Chemical constituents; Ischemic stroke; Anti-inflammatory-immunity; Neuroprotection; Vasodilation; IT-TOF-MSN; FOCAL CEREBRAL-ISCHEMIA; RAT; IDENTIFICATION; METABOLITES; MECHANISMS; GLUTAMATE; CONSTITUENTS; URINE; HIPPOCAMPUS;
D O I
暂无
中图分类号
R [医药、卫生];
学科分类号
100218 [急诊医学];
摘要
Buyang Huanwu Decoction (BYHWD) is a well-known traditional Chinese medicine prescription which is used to treat ischaemic stroke and stroke-induced disabilities. However, the exact mechanism underlying BYHWD's amelioration of ischaemic stroke and its effective constituents remain unclear. The present study aimed to identify the effective constituents of BYHWD and to further explore its action mechanisms in the amelioration of ischaemic stroke by testing the activities of 15 absorbable chemical constituents of BYHWD with the same methods under the same conditions. The following actions of these 15 compounds were revealed: 1) Ferulic acid, calycosin, formononetin, astrapterocarpan-3-O-beta-D-glucoside, paeonol, calycosin-7-O-beta-D-glucoside, astraisoflavan-7-O-beta-D-glucoside, ligustrazine, and propyl gallate significantly suppressed concanavalin A (Con A)-induced T lymphocyte proliferation; 2) Propyl gallate, calycosin-7-O-beta-D-glucoside, paeonol, and ferulic acid markedly inhibited LPS-induced apoptosis in RAW264.7 cells; 3) Propyl gallate and formononetin significantly inhibited LPS-induced NO release; 4) Hydroxysafflor yellow A and inosine protected PC12 cells against the injuries caused by glutamate; and 5) Formononetin, astragaloside IV, astraisoflavan-7-O-beta-Dglucoside, inosine, paeoniflorin, ononin, paeonol, propyl gallate, ligustrazine, and ferulic acid significantly suppressed the constriction of the thoracic aorta induced by KCl in rats. In conclusion, the results from the present study suggest that BYHWD exerts its ischaemic stroke ameliorating activities by modulating multiple targets with multiple components.
引用
收藏
页码:194 / 202
页数:9
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