POLYETHYLENE GLYCOL-CONJUGATED SUPEROXIDE-DISMUTASE IN FOCAL CEREBRAL ISCHEMIA-REPERFUSION

被引:98
作者
HE, YY
HSU, CY
EZRIN, AM
MILLER, MS
机构
[1] BAYLOR COLL MED, DIV RESTORAT NEUROL, 1 BAYLOR PLAZA, HOUSTON, TX 77030 USA
[2] STERLING WINTHROP RES INST, RENSSELAER, NY 12144 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1993年 / 265卷 / 01期
关键词
FREE RADICALS; INFARCTION; RAT; STROKE; 2,3,5-TRIPHENYLTETRAZOLIUM CHLORIDE;
D O I
10.1152/ajpheart.1993.265.1.H252
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Generation of free radicals during reperfusion after organ ischemia has been implicated in the pathogenesis of ischemic injury. We have previously shown that a combination of intravenous polyethylene glycol-conjugated superoxide dismutase (PEG-SOD) and catalase (PEG-CAT), at a dose of 10,000 U/kg each, is effective in reducing infarct size in a focal cerebral ischemia model in the rat. It is not clear whether PEG-SOD alone is sufficient to reduce ischemic brain injury. In this study we determined the therapeutic efficacy of PEG-SOD and its dose-response curve. In a range of 1,000-30,000 U/kg, PEG-SOD exhibited a U-shaped dose-response curve. Only 10,000 U/kg significantly reduced infarct size [control 121 +/- 12 mm3 (mean +/- SE), n = 35; PEG-SOD 95 +/- 10 mm3, n = 36, P < 0.05]. PEG-SOD at the doses tested did not have significant acute hemodynamic effects but had a tendency to improve postischemic hypotension. This beneficial effect of PEG-SOD on blood pressure did not appear to fully account for the treatment effect of PEG-SOD on infarct size. The narrow therapeutic dose range of PEG-SOD in this study and similar findings of SOD in other investigations may contribute to the inconsistent protective effects of SOD preparations in ischemia-reperfusion injury in the literature.
引用
收藏
页码:H252 / H256
页数:5
相关论文
共 32 条
[1]   EFFECT OF A SUPEROXIDE-DISMUTASE DERIVATIVE ON COLD-INDUCED BRAIN EDEMA [J].
ANDO, Y ;
INOUE, M ;
HIROTA, M ;
MORINO, Y ;
ARAKI, S .
BRAIN RESEARCH, 1989, 477 (1-2) :286-291
[2]  
BECKMAN JS, 1988, J BIOL CHEM, V263, P6884
[3]   REPERFUSION ARRHYTHMIAS - DOSE-RELATED PROTECTION BY ANTI-FREE RADICAL INTERVENTIONS [J].
BERNIER, M ;
MANNING, AS ;
HEARSE, DJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (05) :H1344-H1352
[4]   PROTECTIVE EFFECTS OF LIPOSOME-ENTRAPPED SUPEROXIDE-DISMUTASE ON POSTTRAUMATIC BRAIN EDEMA [J].
CHAN, PH ;
LONGAR, S ;
FISHMAN, RA .
ANNALS OF NEUROLOGY, 1987, 21 (06) :540-547
[5]   REDUCTION OF ACTIVITIES OF SUPEROXIDE-DISMUTASE BUT NOT OF GLUTATHIONE-PEROXIDASE IN RAT-BRAIN REGIONS FOLLOWING DECAPITATION ISCHEMIA [J].
CHAN, PH ;
CHU, L ;
FISHMAN, RA .
BRAIN RESEARCH, 1988, 439 (1-2) :388-390
[6]   A MODEL OF FOCAL ISCHEMIC STROKE IN THE RAT - REPRODUCIBLE EXTENSIVE CORTICAL INFARCTION [J].
CHEN, ST ;
HSU, CY ;
HOGAN, EL ;
MARICQ, H ;
BALENTINE, JD .
STROKE, 1986, 17 (04) :738-743
[7]   EFFECT OF SUPEROXIDE-DISMUTASE ON MYOCARDIAL INFARCT SIZE IN THE CANINE HEART AFTER 6 HOURS OF REGIONAL ISCHEMIA AND REPERFUSION - A DEMONSTRATION OF MYOCARDIAL SALVAGE [J].
CHI, L ;
TAMURA, Y ;
HOFF, PT ;
MACHA, M ;
GALLAGHER, KP ;
SCHORK, MA ;
LUCCHESI, BR .
CIRCULATION RESEARCH, 1989, 64 (04) :665-675
[8]  
Elstner E.F., 1983, METHOD ENZYMAT AN, P293
[9]   SUPEROXIDE-DISMUTASE AND CATALASE FAILED TO IMPROVE NEUROLOGIC OUTCOME AFTER COMPLETE CEREBRAL-ISCHEMIA IN THE DOG [J].
FORSMAN, M ;
FLEISCHER, JE ;
MILDE, JH ;
STEEN, PA ;
MICHENFELDER, JD .
ACTA ANAESTHESIOLOGICA SCANDINAVICA, 1988, 32 (02) :152-155
[10]   POLYETHYLENE-GLYCOL CONJUGATED SUPEROXIDE-DISMUTASE FAILS TO AUGMENT BRAIN SUPEROXIDE-DISMUTASE ACTIVITY IN PIGLETS [J].
HAUN, SE ;
KIRSCH, JR ;
HELFAER, MA ;
KUBOS, KL ;
TRAYSTMAN, RJ .
STROKE, 1991, 22 (05) :655-659