Spatial and temporal patterns of oxidative stress in the brain of gerbils submitted to different duration of global cerebral ischemia

被引:30
作者
Selakovic, Vesna [2 ]
Korenic, Andrej [1 ]
Radenovic, Lidija [1 ]
机构
[1] Univ Belgrade, Dept Physiol & Biochem, Fac Biol, Belgrade 11000, Serbia
[2] MMA, Inst Med Res, Belgrade, Serbia
关键词
Brain; Gerbils; Nitric oxide; Reactive oxygen species; Stroke; Reperfusion; LIPID-PEROXIDATION; NITRIC-OXIDE; TIME-COURSE; SUPEROXIDE; DAMAGE; INJURY; MITOCHONDRIA; DISEASE; GLUTATHIONE; REGIONS;
D O I
10.1016/j.ijdevneu.2011.02.009
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The present study was undertaken to examine spatial and temporal patterns of oxidative stress rate in the brain of Mongolian gerbils submitted to different duration of global ischemia/reperfusion. The common carotid arteries of gerbils were occluded for 5, 10, or 15 min. We followed the temporal ischemia-induced oxidative stress rate, the most important factor that exacerbates brain damage by reperfusion, starting from 24 h up to 28 days after reperfusion. The spatial ischemia-induced oxidative stress distribution was measured parallely in different brain regions: forebrain cortex, striatum, hippocampus and cerebellum. Post-ischemic effects were followed in vivo by monitoring the neurological status of whole animals and at the intracellular level by standard biochemical assays in different brain regions. We measured superoxide production, superoxide dismutase activity, nitric oxide production, index of lipid peroxidation, and reduced glutathione. Our results revealed a pattern of dynamic changes in each oxidative stress parameter that corresponded with ischemia duration in all tested brain structures. The highest levels were obtained in the first 24 h after the insult. After that, they slowly returned to nearly control values 28 days after reperfusion (with the exception of SOD activity that returned to control values at fourth day after reperfusion). The most sensitive oxidative stress parameter was index of lipid peroxidation. Our study confirmed spatial distribution of ischemia-induced oxidative stress. Tested brain structures showed different sensitivity to each oxidative stress parameter, although their basal levels were similar. These new findings could be valuable for creation and strategy of post-ischemic therapy. (C) 2011 ISDN. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:645 / 654
页数:10
相关论文
共 37 条
[1]   Down regulation of cerebellar serotonergic receptors in streptozotocin induced diabetic rats: Effect of pyridoxine and Aegle marmelose [J].
Abraham, Pretty Mary ;
Paul, Jes ;
Paulose, C. S. .
BRAIN RESEARCH BULLETIN, 2010, 82 (1-2) :87-94
[2]  
Anderson M.E., 1985, HDB METHODS OXYGEN R, P317
[3]   APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE [J].
BECKMAN, JS ;
BECKMAN, TW ;
CHEN, J ;
MARSHALL, PA ;
FREEMAN, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1620-1624
[4]   Xanthine oxidase-derived superoxide causes reoxygenation injury of ischemic cerebral endothelial cells [J].
Beetsch, JW ;
Park, TS ;
Dugan, LL ;
Shah, AR ;
Gidday, JM .
BRAIN RESEARCH, 1998, 786 (1-2) :89-95
[5]   Behavioral effects and oxidative status in brain regions of adult rats exposed to BDE-99 [J].
Belles, Montserrat ;
Alonso, Virginia ;
Linares, Victoria ;
Albina, Maria L. ;
Sirvent, Juan J. ;
Domingo, Jose L. ;
Sanchez, Domenec J. .
TOXICOLOGY LETTERS, 2010, 194 (1-2) :1-7
[6]   PTU-induced hypothyroidism modulates antioxidant defence status in the developing cerebellum [J].
Bhanja, S. ;
Chainy, G. B. N. .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2010, 28 (03) :251-262
[7]   Nitric oxide acutely inhibits neuronal energy production [J].
Brorson, JR ;
Schumacker, PT ;
Zhang, H .
JOURNAL OF NEUROSCIENCE, 1999, 19 (01) :147-158
[8]   Time course of oxidative damage in different brain regions following transient cerebral ischemia in gerbils [J].
Candelario-Jalil, E ;
Mhadu, NH ;
Al-Dalain, SM ;
Martínez, G ;
León, OS .
NEUROSCIENCE RESEARCH, 2001, 41 (03) :233-241
[9]   Reactive oxygen radicals in signaling and damage in the ischemic brain [J].
Chan, PH .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2001, 21 (01) :2-14
[10]   Differential role of superoxide and glutathione in S-nitrosoglutathione-mediated apoptosis:: a rationale for mild forms of familial amyotrophic lateral sclerosis associated with less active Cu,Zn superoxide dismutase mutants [J].
Ciriolo, MR ;
Aquilano, K ;
De Martino, A ;
Carrì, MT ;
Rotilio, G .
JOURNAL OF NEUROCHEMISTRY, 2001, 77 (06) :1433-1443