Controlled reperfusion of cardiac grafts from non-heart-beating donors

被引:9
作者
Cope, JT [1 ]
Mauney, MC [1 ]
Banks, D [1 ]
Binns, OAR [1 ]
deLima, NF [1 ]
Buchanan, SA [1 ]
Shockey, KS [1 ]
Wilson, SW [1 ]
Kron, IL [1 ]
Tribble, CG [1 ]
机构
[1] UNIV VIRGINIA,CTR HLTH SCI,DEPT SURG,DIV THORAC & CARDIOVASC SURG,CHARLOTTESVILLE,VA 22908
关键词
D O I
10.1016/0003-4975(96)00541-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Hearts harvested from non-heart-beating donors sustain severe injury during procurement and implantation, mandating interventions to preserve their function. We tested the hypothesis that limiting oxygen delivery during initial reperfusion of such hearts would reduce free-radical injury. Methods. Rabbits sustained hypoxic arrest after ventilatory withdrawal, followed by 20 minutes of in vivo ischemia. Hearts were excised and reperfused with blood under conditions of high arterial oxygen tension (PaO2) (approximately 400 mm Hg), high pressure (80 mm Hg), and low pressure (40 mm Hg), with or without free-radical scavenger infusion. Non-heart-beating donor groups were defined by the initial reperfusion conditions: high PaO2/high pressure (n = 8), low PaO2/high pressure (n = 7), high PaO2/low pressure (n = 8), low PaO2/low pressure (n = 7), and high PaO2/high pressure/free-radical scavenger infusion (n = 7). Results. After 45 minutes of reperfusion, low PaO2/high pressure and high PaO2/low pressure had a significantly higher left ventricular developed pressure (63.6 +/- 5.6) and 63.1 +/- 5.6 mm Hg, respectively) than high PaO2/high pressure (40.9 +/- 4.5 mm Hg; p < 0.0000001 versus both). However, high PaO2/high pressure/free-radical scavenger infusion displayed only a trend toward improved ventricular recovery compared with high PaO2/high pressure. Conclusion. Initially reperfusing nonbeating cardiac grafts at low PaO2 or low pressure improves recovery, but may involve mechanisms other than decreased free-radical injury.
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收藏
页码:1418 / 1423
页数:6
相关论文
共 19 条
[1]   EVIDENCE FOR A REVERSIBLE OXYGEN RADICAL MEDIATED COMPONENT OF REPERFUSION INJURY - REDUCTION BY RECOMBINANT HUMAN SUPEROXIDE-DISMUTASE ADMINISTERED AT THE TIME OF REFLOW [J].
AMBROSIO, G ;
WEISFELDT, ML ;
JACOBUS, WE ;
FLAHERTY, JT .
CIRCULATION, 1987, 75 (01) :282-291
[2]   MARKED REDUCTION OF FREE-RADICAL GENERATION AND CONTRACTILE DYSFUNCTION BY ANTIOXIDANT THERAPY BEGUN AT THE TIME OF REPERFUSION - EVIDENCE THAT MYOCARDIAL STUNNING IS A MANIFESTATION OF REPERFUSION INJURY [J].
BOLLI, R ;
JEROUDI, MO ;
PATEL, BS ;
ARUOMA, OI ;
HALLIWELL, B ;
LAI, EK ;
MCCAY, PB .
CIRCULATION RESEARCH, 1989, 65 (03) :607-622
[3]   NITRIC-OXIDE ATTENUATES CARDIAC MYOCYTE CONTRACTION [J].
BRADY, AJB ;
WARREN, JB ;
POOLEWILSON, PA ;
WILLIAMS, TJ ;
HARDING, SE .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (01) :H176-H182
[4]   SUCCESSFUL TRANSPLANTATION OF HEARTS HARVESTED 30 MINUTES AFTER DEATH FROM EXSANGUINATION [J].
GUNDRY, SR ;
DEBEGONA, JA ;
KAWAUCHI, M ;
BAILEY, LL .
ANNALS OF THORACIC SURGERY, 1992, 53 (05) :772-775
[5]  
GUNDRY SR, 1993, ARCH SURG-CHICAGO, V128, P989
[6]  
HOSENPUD JD, 1994, J HEART LUNG TRANSPL, V13, P561
[7]   STUDIES OF HYPOXEMIC/REOXYGENATION INJURY - WITHOUT AORTIC CLAMPING .13. INTERACTION BETWEEN OXYGEN-TENSION AND CARDIOPLEGIC COMPOSITION IN LIMITING NITRIC-OXIDE PRODUCTION AND OXIDANT DAMAGE [J].
IHNKEN, K ;
MORITA, K ;
BUCKBERG, GD ;
SHERMAN, MP ;
IGNARRO, LJ ;
YOUNG, HH .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1995, 110 (04) :1274-1286
[8]   THE RELATION OF FREE-RADICAL PRODUCTION TO HYPEROXIA [J].
JAMIESON, D ;
CHANCE, B ;
CADENAS, E ;
BOVERIS, A .
ANNUAL REVIEW OF PHYSIOLOGY, 1986, 48 :703-719
[9]   TRANSMURAL GRADIENT IN HIGH-ENERGY PHOSPHATE CONTENT IN PATIENTS WITH CORONARY-ARTERY DISEASE [J].
JONES, RN ;
PEYTON, RB ;
SABINA, RL ;
SWAIN, JL ;
HOLMES, EW ;
SPRAY, TL ;
VANTRIGT, P ;
WECHSLER, AS .
ANNALS OF THORACIC SURGERY, 1981, 32 (06) :546-552
[10]   PROTECTION AGAINST POSTISCHEMIC MYOCARDIAL DYSFUNCTION IN ANESTHETIZED RABBITS WITH SCAVENGERS OF OXYGEN-DERIVED FREE-RADICALS - SUPEROXIDE-DISMUTASE PLUS CATALASE, N-2-MERCAPTOPROPIONYL GLYCINE AND CAPTOPRIL [J].
KOERNER, JE ;
ANDERSON, BA ;
DAGE, RC .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1991, 17 (02) :185-191