Wei, H., Xiao-jun, X. Attenuation of brain inflammatory response after focal cerebral ischemia/reperfusion with Xuesaitong Injection in rats., Chin. J. Integr. Med. 12, 203–206 (2006). https://doi.org/10.1007/BF02836523
He Wei, Xu Xiao-jun. Attenuation of brain inflammatory response after focal cerebral ischemia/reperfusion with Xuesaitong Injection in rats[J]. Chinese Journal of Integrative Medicine, 2006,12(3):203-206.
Wei, H., Xiao-jun, X. Attenuation of brain inflammatory response after focal cerebral ischemia/reperfusion with Xuesaitong Injection in rats., Chin. J. Integr. Med. 12, 203–206 (2006). https://doi.org/10.1007/BF02836523DOI:
He Wei, Xu Xiao-jun. Attenuation of brain inflammatory response after focal cerebral ischemia/reperfusion with Xuesaitong Injection in rats[J]. Chinese Journal of Integrative Medicine, 2006,12(3):203-206. DOI: 10.1007/BF02836523.
Attenuation of brain inflammatory response after focal cerebral ischemia/reperfusion with Xuesaitong Injection in rats
摘要
Objective: To investigate the neuro-protective effect of Xuesaitong Injection XST on brain inflammatory response after transient focal cerebral ischemia/reperfusion in rats.Methods: Focal cerebral ischemia/reperfusion models of male rats were induced by transient occlusion for 2 h of middle cerebral artery (MCA) which was followed by 24 h reperfusion. XST was administered through intraperitoneal injection of 25 mg/kg or 50 mg/kg at 4 h after the onset of ischemia. After reperfusion for 24 h
the neurological function score was evaluated
the brain edema was detected with dry-wet weight method
the myeloperoxidase (MPO) activity and the expression of intercellular adhesion molecule-1 (ICAM-1) of ischemic cerebral cortex and caudate putamen was determined by spectrophotometry and immunohistochemistry respectively.Results: XST not only lowered neurological function score at the dose of 50 mg/kg
but reduced brain edema and inhibited MPO activity and ICAM-1 expression as compared with the ischemia/reperfusion model group (P < 0.01).Conclusion: XST has a definite effect on inhibiting the expression of ICAM-1 and neutrophil infiltration in rats with cerebral ischemia/reperfusion when treatment started at 4 h after ischemia onset
and also attenuates inflammation in the infarcted cerebral area.
Abstract
Objective: To investigate the neuro-protective effect of Xuesaitong Injection XST on brain inflammatory response after transient focal cerebral ischemia/reperfusion in rats.Methods: Focal cerebral ischemia/reperfusion models of male rats were induced by transient occlusion for 2 h of middle cerebral artery (MCA) which was followed by 24 h reperfusion. XST was administered through intraperitoneal injection of 25 mg/kg or 50 mg/kg at 4 h after the onset of ischemia. After reperfusion for 24 h
the neurological function score was evaluated
the brain edema was detected with dry-wet weight method
the myeloperoxidase (MPO) activity and the expression of intercellular adhesion molecule-1 (ICAM-1) of ischemic cerebral cortex and caudate putamen was determined by spectrophotometry and immunohistochemistry respectively.Results: XST not only lowered neurological function score at the dose of 50 mg/kg
but reduced brain edema and inhibited MPO activity and ICAM-1 expression as compared with the ischemia/reperfusion model group (P < 0.01).Conclusion: XST has a definite effect on inhibiting the expression of ICAM-1 and neutrophil infiltration in rats with cerebral ischemia/reperfusion when treatment started at 4 h after ischemia onset
and also attenuates inflammation in the infarcted cerebral area.
关键词
Xuesaitong Injectiontotal saponins of panax notoginsengCerebral Ischemiabrain injuryneutrophilintercellular adhesion molecule-1
Keywords
Xuesaitong Injectiontotal saponins of panax notoginsengCerebral Ischemiabrain injuryneutrophilintercellular adhesion molecule-1
references
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相关作者
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相关机构
Department of Neurology, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine
Key Laboratory of Neurodegenerative Diseases (Capital Medical University), Ministry of Education
Cerebrovascular Diseases Research Institute, Xuanwu Hospital of Capital Medical University
Department of Neurology, Xuanwu Hospital of Capital Medical University
Faculty of Chinese Medicine, Macau University of Science and Technology, Macao