Folium Ginkgo extract and tetramethylpyrazine sodium chloride injection (Xingxiong injection) protects against focal cerebral ischaemia/reperfusion injury via activating the Akt/Nrf2 pathway and inhibiting NLRP3 inflammasome activation

被引:25
作者
Zhu, Ting [1 ,2 ,3 ,4 ,5 ]
Fang, Bin-Yu [1 ,2 ,3 ,4 ,6 ]
Meng, Xiang-Bao [1 ,2 ,3 ,4 ]
Zhang, Shu-Xia [1 ,2 ,3 ,4 ]
Wang, Hong [7 ]
Gao, Ge [7 ]
Liu, Fei [7 ]
Wu, Yu [7 ]
Hu, Jin [7 ]
Sun, Gui-Bo [1 ,2 ,3 ,4 ]
Sun, Xiao-Bo [1 ,2 ,3 ,4 ]
机构
[1] Beijing Key Lab Innovat Drug Discovery Tradit Chi, Beijing, Peoples R China
[2] Minist Educ, Key Lab Bioact Subst & Resources Utilizat Chinese, Beijing, Peoples R China
[3] Key Lab New Drug Discovery Based Class Chinese Me, Beijing, Peoples R China
[4] Chinese Acad Med Sci & Peking Union Med Coll, Inst Med Plant Dev, NMPA Key Lab Res & Evaluat Pharmacovigilance, Beijing, Peoples R China
[5] Qingdao Univ, Inst Neuroregenerat & Neurorehabil, Qingdao, Peoples R China
[6] Harbin Univ Commerce, Harbin, Peoples R China
[7] Sihuan Pharmaceut Holdings Grp Ltd, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Ischaemic stroke; apoptosis; inflammation; oxidative stress; ISCHEMIA/REPERFUSION INJURY; REPERFUSION INJURY; OXIDATIVE STRESS; GINSENOSIDE RB1; ISCHEMIC-STROKE; BRAIN; NEUROPROTECTION; ANGIOGENESIS; ASTROCYTES; TARGETS;
D O I
10.1080/13880209.2021.2014895
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Context Folium Ginkgo extract and tetramethylpyrazine sodium chloride injection (Xingxiong injection) is a compound preparation commonly used for treating cerebral ischaemia/reperfusion injury in ischaemic stroke in China. However, its potential mechanisms on ischaemic stroke remain unknown. Objective This study explores the potential mechanisms of Xingxiong injection in vivo or in vitro. Materials and methods Sprague-Dawley (SD) rats were randomly assigned to five groups: the sham (normal saline), the model (normal saline) and the Xingxiong injection groups (12.5, 25 or 50 mL/kg). The rats were subjected to 2 h of middle cerebral artery occlusion (MCAO) followed by reperfusion for 14 d. Xingxiong injection was administered via intraperitoneal (i.p.) injection immediately after ischaemia induction for 14 d. Afterwards, rats were sacrificed at 14 d induced by administration of Xingxiong injection. Results Xingxiong injection significantly reduces infarct volume (23%) and neurological deficit scores (93%) compared with the MCAO/R group. Additionally, Xingxiong injection inhibits the loss in mitochondrial membrane potential (43%) and reduces caspase-3 level (44%), decreases NOX (41%), protein carbonyl (29%), 4-HNE (40%) and 8-OhdG (41%) levels, inhibits the expression of inflammatory factors, such as TNF-alpha (26%), IL-1 beta (34%), IL-6 (39%), MCP-1 (36%), CD11a (41%) and ICAM-1 (43%). Moreover, Xingxiong injection can increase p-Akt/Akt (35%) and Nrf2 (47%) protein expression and inhibit NLRP3 (42%) protein expression. Conclusions Xingxiong injection prevents cerebral ischaemia/reperfusion injury via activating the Akt/Nrf2 pathway and inhibiting NLRP3 inflammasome. These findings provide experimental evidence for clinical use of drugs in the treatment of ischaemic stroke.
引用
收藏
页码:195 / 205
页数:11
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