Temporal profiles of the levels of endogenous antioxidants after four-vessel occlusion in rats

被引:31
作者
Namba, K [1 ]
Takeda, Y [1 ]
Sunami, K [1 ]
Hirakawa, M [1 ]
机构
[1] Okayama Univ, Sch Med, Dept Anesthesiol & Resuscitol, Okayama 7008558, Japan
关键词
free radical; oxygen stress; superoxide dismutase; glutathione; glutathione peroxidase; catalase; four-vessel occlusion; brain ischemia; antioxidants;
D O I
10.1097/00008506-200104000-00010
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
Although it is known that development of lipid peroxidation after ischemia occurs predominantly in vulnerable regions, temporal profiles of antioxidants after ischemia have not been regionally elucidated. After reperfusion periods of 0, 3, 24, and 72 hours following 20 minutes of four-vessel occlusion (n = 6 in each group), the concentration of total glutathione (GSH) and the activities of superoxide dismutase (SOD), catalase, and glutathione peroxidase (GSH-Px) were assayed in the hippocampus, parietal cortex, striatum, thalamus, and brain stem. The levels of all antioxidants were unchanged in all regions without reperfusion; however, the concentration of total GSH significantly decreased in the hippocampus at 3 hours after the onset of reperfusion, and showed a maximum decrease in the hippocampus (68% of the sham-control level), parietal cortex (78% of the sham-control level), and striatum (76% of the sham-control level) after 24 hours of reperfusion. After 72 hours of reperfusion, these regions and the thalamus showed restoration and an increase in the total GSH concentration, respectively. The activities of SOD, GSH-Px, and catalase were stable during the: reperfusion period, but the hippocampus showed significant increases in these enzyme activities and the parietal cortex and striatum showed significant increases in SOD activities at 72 hours after the onset of reperfusion. These results indicate that endogenous antioxidants take 72 hours for restoration in vulnerable regions after 20 minutes of four-vessel occlusion in rats.
引用
收藏
页码:131 / 137
页数:7
相关论文
共 30 条
[1]
The possible role of endogenous glutathione as an anticonvulsant in mice [J].
Abe, K ;
Nakanishi, K ;
Saito, H .
BRAIN RESEARCH, 2000, 854 (1-2) :235-238
[2]
Aebi HE., 1983, Methods of enzymatic analysis, P273
[3]
ANDERSON ME, 1985, METHOD ENZYMOL, V113, P548
[4]
POLYETHYLENE-GLYCOL SUPEROXIDE-DISMUTASE AND CATALASE ATTENUATE INCREASED BLOOD-BRAIN-BARRIER PERMEABILITY AFTER ISCHEMIA IN PIGLETS [J].
ARMSTEAD, WM ;
MIRRO, R ;
THELIN, OP ;
SHIBATA, M ;
ZUCKERMAN, SL ;
SHANKLIN, DR ;
BUSIJA, DW ;
LEFFLER, CW .
STROKE, 1992, 23 (05) :755-762
[5]
REGIONAL DISTRIBUTION OF CATALASE IN THE ADULT-RAT BRAIN [J].
BRANNAN, TS ;
MAKER, HS ;
RAES, IP .
JOURNAL OF NEUROCHEMISTRY, 1981, 36 (01) :307-309
[6]
REGIONAL DISTRIBUTION OF GLUTATHIONE-PEROXIDASE IN THE ADULT-RAT BRAIN [J].
BRANNAN, TS ;
MAKER, HS ;
WEISS, C ;
COHEN, G .
JOURNAL OF NEUROCHEMISTRY, 1980, 35 (04) :1013-1014
[7]
INCREASED LIPID-PEROXIDATION IN VULNERABLE BRAIN-REGIONS AFTER TRANSIENT FOREBRAIN ISCHEMIA IN RATS [J].
BROMONT, C ;
MARIE, C ;
BRALET, J .
STROKE, 1989, 20 (07) :918-924
[8]
THE ENZYME-SUBSTRATE COMPOUNDS OF BACTERIAL CATALASE AND PEROXIDES [J].
CHANCE, B ;
HERBERT, D .
BIOCHEMICAL JOURNAL, 1950, 46 (04) :402-414
[9]
DISTRIBUTION OF SUPEROXIDE-DISMUTASE, GLUTATHIONE-PEROXIDASE AND CATALASE IN DEVELOPING RAT-BRAIN [J].
DELMAESTRO, R ;
MCDONALD, W .
MECHANISMS OF AGEING AND DEVELOPMENT, 1987, 41 (1-2) :29-38
[10]
REGIONAL PROTEIN-SYNTHESIS IN RAT-BRAIN FOLLOWING ACUTE HEMISPHERIC ISCHEMIA [J].
DIENEL, GA ;
PULSINELLI, WA ;
DUFFY, TE .
JOURNAL OF NEUROCHEMISTRY, 1980, 35 (05) :1216-1226