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金丝桃苷保护大鼠脑缺血再灌注损伤的机制研究
引用本文:江飞飞, 陈志志, 徐晏雯, 万浩芳, 林海燕. 金丝桃苷保护大鼠脑缺血再灌注损伤的机制研究[J]. 中国现代应用药学, 2021, 38(12): 1448-1453. DOI: 10.13748/j.cnki.issn1007-7693.2021.12.007
作者姓名:江飞飞  陈志志  徐晏雯  万浩芳  林海燕
作者单位:衢州市人民医院神经内科, 浙江 衢州 324000;浙江中医药大学, 杭州 310006
基金项目:浙江省自然科学基金探索项目(LQ20H270017)
摘    要:目的 探究金丝桃苷(hyperoside,Hyp)对脑缺血再灌注大鼠脑组织的保护作用及相关机制.方法 采用线栓法建立大脑中动脉闭塞/再灌注(middle cerebral artery occlusion/reperfusion,MCAO/R)大鼠模型,分成假手术组、模型组、Hyp低、中、高剂量组(30,60,120 ...

关 键 词:金丝桃苷  脑缺血再灌注  抗炎  抗凋亡  TLR4/COX-2信号通路
收稿时间:2020-08-30

Study on Mechanism of Hyperoside Protecting Cerebral Ischemia Reperfusion Injury in Rats
JIANG Feifei, CHEN Zhizhi, XU Yanwen, WAN Haofang, LIN Haiyan. Study on Mechanism of Hyperoside Protecting Cerebral Ischemia Reperfusion Injury in Rats[J]. Chinese Journal of Modern Applied Pharmacy, 2021, 38(12): 1448-1453. DOI: 10.13748/j.cnki.issn1007-7693.2021.12.007
Authors:JIANG Feifei  CHEN Zhizhi  XU Yanwen  WAN Haofang  LIN Haiyan
Affiliation:Department of Neurology, Quzhou City People''s Hospital, Quzhou 324000, China;Zhejiang Chinese Medical University, Hangzhou 310006, China
Abstract:OBJECTIVE To investigate the protective effect and mechanism of hyperoside(Hyp) on brain tissue of cerebral ischemia-reperfusion rats. METHODS Rat models of middle cerebral artery occlusion/reperfusion(MCAO/R) were established by bolt-line method and divided into sham operation group, model group and Hyp low, medium and high dose group(30, 60, 120 mg·kg-1). The rats were evaluated by Zea Longa for neurological function and the brain water content was measured. The volume of cerebral infarction in rats was determined by TTC staining, inflammatory factors were detected by ELISA, pathological morphology of neurons in the hippocampus CA1 was observed by HE staining, apoptosis of brain cells was observed by TUNEL staining, and the expressions of TLR4, COX-2 and apoptosis-related proteins were detected by Western blotting. RESULTS Hyp intervention could significantly improve the Zea Longa score of MCAO/R rats(P<0.05), reduce brain water content and cerebral infarction volume, significantly reduce the expression of inflammatory factors(TNF-α, IL-1β, IL-6, ICAM-1, VCAM-1)(P<0.05 or P<0.01), effectively improve the pathological blood changes and apoptosis of neurons in the hippocampus CA1 region, significantly inhibit the expression of TLR4, COX-2, NF-kB, caspase-3, caspase-9 and Bax protein (P<0.05 or P<0.01), and upregulated the expression of Bcl-2 protein(P<0.05). CONCLUSION The protective effect of Hyp on cerebral ischemia-reperfusion injury is related to anti-inflammatory, anti-apoptotic and inhibition of TLR4/COX-2 signaling pathway.
Keywords:hypericin|brain tissue of cerebral ischemia-reperfusion|anti-inflammatory|anti-apoptosis|TLR4/COX-2 signaling pathway
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