Effects of cathepsins B and L inhibition on postischemic protein alterations in the brain

被引:24
作者
Anagli, John [1 ,3 ]
Abounit, Kadija [1 ]
Stemmer, Paul [4 ]
Han, Yuxia [2 ]
Allred, Lisa [1 ]
Weinsheimer, Shantel [1 ]
Movsisyan, Ashkhen [1 ,3 ]
Seyfried, Donald [2 ]
机构
[1] Henry Ford Hosp, Dept Pathol, Detroit, MI 48202 USA
[2] Henry Ford Hosp, Dept Neurosurg, Detroit, MI 48202 USA
[3] Henry Ford Hosp, Proteom Core Facil, Detroit, MI 48202 USA
[4] Wayne State Univ, Prot Interact & Proteom Facil Core, Inst Environm Hlth Sci, Detroit, MI 48202 USA
关键词
albumin; cathepsin B; middle cerebral artery occlusion; neuroprotection; protease inhibitor; rat;
D O I
10.1016/j.bbrc.2007.11.104
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
The effects of selective inhibition of cathepsins B and L on postischemic protein alterations in the brain were investigated in a rat model of middle cerebral artery occlusion (MCAO). Cathepsin B activity increased predominantly in the subcortical region of the ischemic hemisphere where the levels of collapsing mediator response protein 2, heat shock cognate 70 kDa protein, 60 kDa heat shock protein, protein disulfide isomerase A3 and albumin, were found to be significantly elevated. Postischemic treatment with Cbz-Phe-Ser(OBzl)-CHN2, cysteine protease inhibitor 1 (CP-1),reduced infarct volume, neurological deficits and cathepsin B activity as well as the amount of heat shock proteins and albumin found in the brain. Our data strongly suggests that the decrease in heat shock protein levels and the significant reduction of serum albumin leakage into the brain following acute treatment with CP-1 is indicative of less secondary ischemic damage, which ultimately, is related to less cerebral tissue loss and improved neurological recovery of the animals. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:86 / 91
页数:6
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