Recombinant adenoviral expression of dominant negative IκBα protects brain from cerebral ischemic injury

被引:43
作者
Xu, L
Zhan, YT
Wang, YB
Feuerstein, GZ
Wang, XK
机构
[1] Bristol Myers Squibb Co, Dept Cardiovasc Sci, Expt Stn, Wilmington, DE 19880 USA
[2] Bristol Myers Squibb Co, Dept Neurosci, Expt Stn, Wilmington, DE 19880 USA
[3] Univ Maryland, Dept Physiol, Baltimore, MD 21201 USA
关键词
adenovirus; cerebral ischemia; inflammation; I kappa B; NF-kappa B; neuroprotection; rat;
D O I
10.1016/S0006-291X(02)02573-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transcription factor NF-kappaB is associated with inflammatory response and cell survival. Under inactive condition, NF-kappaB is sequestered in the cytoplasm by an anchor protein, inhibitor of NF-kappaB (IkappaB). NF-kappaB was shown to be activated during ischemic brain injury. In the present study we have investigated the role of NF-kappaB in ischemic brain injury using a recombinant adenovirus expressing a dominant negative form of IkappaB (Adv/IkappaBdn) to specifically inhibit NF-kappaB activation. Our data demonstrated that cortical injection of Adv/IkappaBdn significantly reduced ischemic brain injury following permanent occlusion of the middle cerebral artery (MCAO) in rats, showing 55% reduction (p < 0.01, n = 8) in total ischemic lesion or 80% reduction (p < 0.001) in the cortical area with AdV/IkappaBdn expression. Similarly, AdV/IkappaBdn expression significantly decreased neurological deficits (37% reduction, over controls, p < 0.01, n = 8). These data provide further evidence for the role of NF-kappaB/IkappaB in ischemic brain injury and suggest that inhibition of NF-kappaB is neuroprotective in focal stroke. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:14 / 17
页数:4
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