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[1]乌日吉木斯,刘啸轩,苏悦,等.白细胞介素-18在小鼠缺血性脑卒中的损伤作用及其机制[J].天津医科大学学报,2021,27(06):603-607.
 WU Ri-jimusi,LIU Xiao-xuan,SU Yue,et al.The injury effect of interleukin-18 in the mice with ischemic stroke and its mechanism[J].Journal of Tianjin Medical University,2021,27(06):603-607.
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白细胞介素-18在小鼠缺血性脑卒中的损伤作用及其机制(PDF)
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《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]

卷:
27卷
期数:
2021年06期
页码:
603-607
栏目:
基础医学
出版日期:
2021-11-15

文章信息/Info

Title:
The injury effect of interleukin-18 in the mice with ischemic stroke and its mechanism
文章编号:
1006-8147(2021)06-0603-05
作者:
乌日吉木斯1刘啸轩1苏悦1阎涛12
(天津医科大学总医院1.神经病学研究所;2.神经内科,天津300052)
Author(s):
WU Ri-jimusi1LIU Xiao-xuan1SU Yue1YAN Tao12
(1. Tianjin Neurological Institute;2. Department of Neurology,General Hospital,Tianjin Medical University, Tianjin 300052, China)
关键词:
缺血性脑卒中白细胞介素-18炎症小胶质细胞小鼠
Keywords:
ischemic strokeinterleukin-18inflammationmicrogliamice
分类号:
R743.3
DOI:
-
文献标志码:
A
摘要:
目的:探讨白细胞介素(IL)-18在小鼠缺血性脑卒中的损伤作用及其机制。方法:采用C57BL/6J成年雄性小鼠构建光化学法诱导局灶性大脑皮层缺血性脑卒中模型,随机分为对照组、脑梗死组、IL-18分泌型结合蛋白(IL-18BP)治疗组,每组18只。术后14 d进行神经功能评分并进行HE染色测量小鼠脑梗死面积。术后3 d实时荧光定量PCR检测小鼠脑组织中肿瘤坏死因子-α(TNF-α)、IL-1β、IL-6和IL-10的表达,流式细胞术检测小鼠脑组织中小胶质细胞表型。结果:与脑梗死组相比,IL-18BP治疗组神经功能显著改善并且脑梗死面积显著降低(t=2.750、2.235,均P<0.05)。IL-18BP治疗组脑组织中TNF-α、IL-1β和IL-6的表达显著降低(t=3.091、2.328、3.443,均P<0.05),IL-10的表达升高(t=4.997,P<0.05)。与脑梗死组相比,IL-18BP治疗组脑组织中M1型小胶质细胞数量明显降低(t=4.779,P<0.05),M2型小胶质细胞数量明显升高(t=2.619,P<0.05)。结论:在缺血性脑卒中,IL-18可介导免疫炎性损伤并发挥调节作用。
Abstract:
Objective:To investigate the injury effect of interleukin-18(IL-18) in mice with ischemic stroke and its mechanism. Methods: C57BL/6J adult male mice were used to construct a photochemically induced ischemic stroke model,and they were randomly divided into sham group,stroke group,and IL-18BP (IL-18 secretion bound protein) treatment group,18 mice in each group. Neurological function score was performed 14 days after operation,and cerebral infarct size was measured by H&E staining. The expression of inflammatory factors such as tumor necrosis factor-α(TNF-α),interleukin-1β(IL-1β),interleukin-6(IL-6) and interleukin-10(IL-10)in the brain tissues of mice was detected by Quantitative Real-time PCR 3 days after operation,and the microglial cell phenotype in the brain tissues of mice was detected by flow cytometry. Results: Compared with stroke group,neurological function was significantly improved and cerebral infarct size was significantly reduced(t=2.235,P<0.05)in the IL-18BP treatment group.The expression of TNF-α,IL-1β and IL-6 in the IL-18BP treatment group was significantly decreased(t=3.091,2.328,3.443,all P<0.05),while the expression of IL-10 was increased(t=4.997,P<0.05).Compared with stroke group,the number of M1-type microglia was significantly decreased(t=4.779,P<0.05) and the number of M2 microglia was significantly increased(t=2.619,P<0.05) in the IL-18BP treatment group. Conclusion: In ischemic stroke,IL-18 mediates immune inflammatory injury and plays a key regulatory role.

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备注/Memo

备注/Memo:
基金项目 天津市自然科学基金重点项目(17JCZDJC36100) 作者简介 乌日吉木斯(1996-),女,硕士在读,研究方向:神经病学;通信作者:阎涛,E-mail:taoyan@tmu.edu.cn。
更新日期/Last Update: 2021-11-15