Neuroprotective Effect of Xueshuantong for Injection (Lyophilized) in Transient and Permanent Rat Cerebral Ischemia Model

被引:16
|
作者
Wang, Xumei [1 ]
Wang, Shaoxia [1 ]
Wang, Jinxin [1 ]
Guo, Hong [2 ]
Dong, Zhaopeng [3 ]
Chai, Lijuan [2 ]
Hu, Limin [2 ]
Zhang, Yue [2 ]
Wang, Hong [1 ]
Chen, Lu [1 ]
机构
[1] Tianjin Univ Tradit Chinese Med, Tianjin State Key Lab Modern Chinese Med, Tianjin 300193, Peoples R China
[2] Tianjin Univ Tradit Chinese Med, Tianjin Key Lab Chinese Med Pharmacol, Tianjin 300193, Peoples R China
[3] CSPC Zhongnuo Pharmaceut Shijiazhuang Co Ltd, Zhongnuo R&D Dept, Shijiazhuang 050051, Hebei, Peoples R China
关键词
FREE-RADICAL SCAVENGER; TOLL-LIKE RECEPTORS; PLASMINOGEN-ACTIVATOR; STROKE; BRAIN; INJURY; INFLAMMATION; EDARAVONE; THERAPY; NEUROGENESIS;
D O I
10.1155/2015/134685
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Xueshuantong for Injection (Lyophilized) (XST), a Chinese Materia Medica standardized product extracted from Panax notoginseng (Burk.), is used extensively for the treatment of cerebrovascular diseases such as acutely cerebral infarction clinically in China. In the present study, we evaluated the acute and extended protective effects of XST in different rat cerebral ischemic model and explored its effect on peroxiredoxin (Prx) 6-toll-like receptor (TLR) 4 signaling pathway. We found that XST treatment for 3 days could significantly inhibit transient middle cerebral artery occlusion (MCAO) induced infarct volume and swelling percent and regulate them RNA expression of interleukin-1 beta (IL-1 beta), IL-17, IL-23p19, tumor necrosis factor-alpha (TNF alpha), and inducible nitric oxide synthase (iNOS) in brain. Further study demonstrated that treatment with XST suppressed the protein expression of peroxiredoxin (Prx) 6-toll-like receptor (TLR) 4 and phosphorylation level of p38 and upregulated the phosphorylation level of STAT3. In permanent MCAO rats, XST could reduce the infarct volume and swelling percent. Moreover, our results revealed that XST treatment could increase the rats' weight and improve a batch of functional outcomes. In conclusion, the present data suggested that XST could protect against ischemia injury in transient and permanent MCAO rats, which might be related to Prx6-TLR4 pathway.
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页数:13
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