Enhanced glial activation and expression of specific CNS inflammation-related molecules in aged versus young rats following cortical stab injury

被引:102
作者
Kyrkanides, S
O'Banion, MK
Whiteley, PE
Daeschner, JC
Olschowka, JA
机构
[1] Univ Rochester, Dept Neurobiol & Anat, Rochester, NY 14642 USA
[2] Univ Rochester, Sch Med & Dent, Dept Neurol, Rochester, NY 14642 USA
[3] Roche Biosci, Dept Inflammatory Dis, Palo Alto, CA 94394 USA
关键词
microglia; astrocytes; aging; brain trauma; neurodegenerative disease;
D O I
10.1016/S0165-5728(01)00404-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aging is associated with increased glial responsiveness that may enhance the brain's susceptibility to injury and disease. To determine whether unique age-related molecular responses occur in brain injury, we assessed m-RNA levels of representative central nervous system (CNS) inflammation-related molecules in young (3 months) and aged (36 months) Fisher 344/Brown Norwegian F1 hybrid rats following cortical stab. Enhanced glial activation in older animals was accompanied by increased expression of a subset of inflammation-related mRNAs, including IL-1 beta, TNF alpha, IL-6, ICAM-1, inducible nitric oxide synthase (iNOS), metalloprotednase-9 (NEAP-9), and complement 3 alpha -chain 1 (C3 alpha1). Recognition of these age-specific differences may guide development of novel treatment regimes for older individuals. (C) 2001 Elsevier Science BY. All rights reserved.
引用
收藏
页码:269 / 277
页数:9
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