CATECHOL ADRENERGIC AGENTS ENHANCE HYDROXYL RADICAL GENERATION IN XANTHINE-OXIDASE SYSTEMS CONTAINING FERRITIN - IMPLICATIONS FOR ISCHEMIA-REPERFUSION

被引:36
作者
ALLEN, DR
WALLIS, GL
MCCAY, PB
机构
[1] OKLAHOMA MED RES FDN, FREE RADICAL BIOL & AGING RES PROGRAM, OKLAHOMA CITY, OK 73104 USA
[2] UNIV OKLAHOMA, DEPT MED, PULM & CRIT CARE MED SECT, OKLAHOMA CITY, OK 73109 USA
关键词
FERRITIN; IRON; CATECHOLAMINES; ISCHEMIA; FREE RADICALS; XANTHINE OXIDASE;
D O I
10.1006/abbi.1994.1495
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
Iron chelators have been reported to protect tissues against reperfusion injury. This implies that iron is being released into the plasma or is made accessible in tissues for oxidation-reduction reactions. It has been postulated that ferritin is a likely source for this iron. This report demonstrates that adrenergic agents with the catechol structure, which includes the endogenous catecholamines norepinephrine and epinephrine, are capable of releasing iron from ferritin. It is shown that the net release of iron from ferritin by epinephrine is significantly enhanced under anaerobic conditions. The findings suggest that catecholamines can mediate iron release from ferritin under conditions that can occur during ischemia/reperfusion. Catecholamines are also shown to interact with the released iron and xanthine oxidase to produce highly reactive hydroxyl radicals. The implications of this interaction for ischemia/reperfusion are discussed. (C) 1994 Academic Press, Inc.
引用
收藏
页码:235 / 243
页数:9
相关论文
共 45 条
[1]   IMPROVEMENT OF POSTISCHEMIC MYOCARDIAL-FUNCTION AND METABOLISM INDUCED BY ADMINISTRATION OF DEFEROXAMINE AT THE TIME OF REFLOW - THE ROLE OF IRON IN THE PATHOGENESIS OF REPERFUSION INJURY [J].
AMBROSIO, G ;
ZWEIER, JL ;
JACOBUS, WE ;
WEISFELDT, ML ;
FLAHERTY, JT .
CIRCULATION, 1987, 76 (04) :906-915
[2]   PROTECTION FROM REPERFUSION INJURY IN THE ISOLATED RAT-HEART BY POSTISCHEMIC DEFEROXAMINE AND OXYPURINOL ADMINISTRATION [J].
BADYLAK, SF ;
SIMMONS, A ;
TUREK, J ;
BABBS, CF .
CARDIOVASCULAR RESEARCH, 1987, 21 (07) :500-506
[3]   SUPEROXIDE-DEPENDENT AND SUPEROXIDE-INDEPENDENT MECHANISMS OF IRON MOBILIZATION FROM FERRITIN BY XANTHINE-OXIDASE - IMPLICATIONS FOR OXYGEN-FREE-RADICAL-INDUCED TISSUE DESTRUCTION DURING ISCHEMIA AND INFLAMMATION [J].
BIEMOND, P ;
SWAAK, AJG ;
BEINDORFF, CM ;
KOSTER, JF .
BIOCHEMICAL JOURNAL, 1986, 239 (01) :169-173
[4]   RELEASE OF IRON FROM FERRITIN BY XANTHINE-OXIDASE - ROLE OF THE SUPEROXIDE RADICAL [J].
BOLANN, BJ ;
ULVIK, RJ .
BIOCHEMICAL JOURNAL, 1987, 243 (01) :55-59
[5]  
BOLANN BJ, 1990, FEBS LETT, P899
[6]   EFFECT OF SUPEROXIDE-DISMUTASE ON THE AUTOXIDATION OF VARIOUS HYDROQUINONES - A POSSIBLE ROLE OF SUPEROXIDE-DISMUTASE AS A SUPEROXIDE SEMIQUINONE OXIDOREDUCTASE [J].
CADENAS, E ;
MIRA, D ;
BRUNMARK, A ;
LIND, C ;
SEGURAAGUILAR, J ;
ERNSTER, L .
FREE RADICAL BIOLOGY AND MEDICINE, 1988, 5 (02) :71-79
[7]   RELEASE OF ENDOGENOUS CATECHOLAMINES IN THE ISCHEMIC MYOCARDIUM OF THE RAT .B. EFFECT OF SYMPATHETIC-NERVE STIMULATION [J].
DART, AM ;
SCHOMIG, A ;
DIETZ, R ;
MAYER, E ;
KUBLER, W .
CIRCULATION RESEARCH, 1984, 55 (05) :702-706
[8]  
DINARELLO CA, 1992, CECIL TXB MED, P1571
[9]  
Fairbanks V F, 1983, HEMATOLOGY, P300
[10]   EVIDENCE FOR A ROLE OF IRON-CATALYZED OXIDANTS IN FUNCTIONAL AND METABOLIC STUNNING IN THE CANINE HEART [J].
FARBER, NE ;
VERCELLOTTI, GM ;
JACOB, HS ;
PIEPER, GM ;
GROSS, GJ .
CIRCULATION RESEARCH, 1988, 63 (02) :351-360