Microglial response to early ischemia‐induced changes in the rat spinal cord

K. Saganová, J. Mars̆ala, T. Ondrejčák, I. Vanický, J. Gálik
{"title":"Microglial response to early ischemia‐induced changes in the rat spinal cord","authors":"K. Saganová, J. Mars̆ala, T. Ondrejčák, I. Vanický, J. Gálik","doi":"10.1002/NRC.10094","DOIUrl":null,"url":null,"abstract":"We examined the early microglial response to spinal cord ischemia induced by occlusion of the descending aorta for 15 min, or more limited aortic occlusion (8, 10, 12 min( linked with blood volume reduction. The recovery of motor function and activation of microglia labeled by Griffonia simplicifolia B4-isolectin (GSA I-B4-HRP) were assessed up to 7 days post-ischemia. Activation of resident microglia characterized by both increased lectin binding and altered morphology was observed >48 hrs post-ischemia. Massive infiltration of the microglia/macrophages related to the severity of ischemic insult appeared at day 3. Our data suggest that (1) ischemia of different degrees gives rise to a generalized microglial response at the early post-ischemic phase; (2) graded activation of microglia/macrophases as a response to ischemic neuronal injury occurs within 48–72 hrs of post-ischemic reperfusion; (3) lectin labeling of microglia can serve for continuous study of the evolution of pathological changes associated with transient spinal cord ischemia.","PeriodicalId":19198,"journal":{"name":"Neuroscience Research Communications","volume":"38 1","pages":"179-188"},"PeriodicalIF":0.0000,"publicationDate":"2003-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuroscience Research Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/NRC.10094","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

We examined the early microglial response to spinal cord ischemia induced by occlusion of the descending aorta for 15 min, or more limited aortic occlusion (8, 10, 12 min( linked with blood volume reduction. The recovery of motor function and activation of microglia labeled by Griffonia simplicifolia B4-isolectin (GSA I-B4-HRP) were assessed up to 7 days post-ischemia. Activation of resident microglia characterized by both increased lectin binding and altered morphology was observed >48 hrs post-ischemia. Massive infiltration of the microglia/macrophages related to the severity of ischemic insult appeared at day 3. Our data suggest that (1) ischemia of different degrees gives rise to a generalized microglial response at the early post-ischemic phase; (2) graded activation of microglia/macrophases as a response to ischemic neuronal injury occurs within 48–72 hrs of post-ischemic reperfusion; (3) lectin labeling of microglia can serve for continuous study of the evolution of pathological changes associated with transient spinal cord ischemia.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
小胶质细胞对早期缺血引起的大鼠脊髓变化的反应
我们检查了早期小胶质细胞对降主动脉阻断15分钟或更有限的主动脉阻断(8、10、12分钟)引起的脊髓缺血的反应(与血容量减少有关)。在缺血后7天,观察运动功能的恢复情况和单纯Griffonia B4-isolectin (GSA I-B4-HRP)标记的小胶质细胞活化情况。缺血后>48小时,观察到以凝集素结合增加和形态改变为特征的常驻小胶质细胞活化。第3天出现与缺血性损伤严重程度相关的小胶质细胞/巨噬细胞的大量浸润。我们的数据表明:(1)不同程度的缺血会在缺血后早期引起广泛的小胶质细胞反应;(2)在缺血再灌注后48-72小时内,小胶质细胞/大相对缺血性神经元损伤的反应发生分级激活;(3)对小胶质细胞进行凝集素标记,可为持续研究短暂性脊髓缺血相关病理变化的演变提供依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Advance on the diagnostic potential of biological markers in the early detection of Alzheimer Disease The potential role played by artificial adaptive systems in enhancing our understanding of Alzheimer disease: The experience gained within Italian Interdisciplinary network on Alzheimer disease Phosphorylation of the amyloid precursor protein (APP): Is this a mechanism in favor or against Alzheimer's disease? Behavioural and psychological symptoms of dementia: clinical aspects Oxidative stress in Alzheimer's disease: a selective status report
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1