VASODILATORY AND TOXIC EFFECTS OF SPIN TRAPS ON AEROBIC CARDIAC-FUNCTION

被引:64
作者
KONOREV, EA
BAKER, JE
JOSEPH, J
KALYANARAMAN, B
机构
[1] MED COLL WISCONSIN,BIOPHYS RES INST,8701 WATERTOWN PLANK RD,MILWAUKEE,WI 53226
[2] MED COLL WISCONSIN,DEPT CARDIOTHORAC SURG,MILWAUKEE,WI 53226
关键词
SPIN TRAPS; ISOLATED RAT HEART; FREE RADICAL; VENTRICULAR FUNCTION; CORONARY FLOW;
D O I
10.1016/0891-5849(93)90003-D
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
The objective of this study was to compare the effect of several structurally related nitrone and nitroso spin traps on the function of the isolated bicarbonate-buffer perfused rat heart model. Spin traps investigated were alpha-phenyl-tert-butyl N-nitrone (PBN), alpha-(4-pyridyl-1-oxide)-N-tert-butyl nitrone (POBN), 2-methyl-2-nitroso propane (MNP), 2-hydroxymethyl-2-nitroso propane (MNP/OH), nitrosobenzene (NB), dibromonitrosobenzene-sulfonic acid (DBNBS), and 5,5-dimethyl-1-pyrroline-N-oxide (DMPO). During perfusion of hearts with increasing concentrations of spin traps, ventricular pressure, coronary flow rate, and heart rate were continuously recorded. The extent of contractile recovery was subsequently measured upon return to spin-trap free perfusion. The percentage of maximum increase in coronary flow with PBN, POBN, MNP, MNP-OH, NB, DBNBS, and DMPO were 11, 40, 45, 66, 28, 28, and 29%, respectively. Thus, all nitroso and nitrone spin traps studied acted as vasodilators. Over the dose range studied, POBN, MNP, MNP/OH, and DMPO did not exert any chronotropic effect. PBN, NB, and DBNBS exerted a negative chronotropic effect at higher concentrations. All spin traps studied, with the exception of DMPO, exerted a negative inotropic effect at the higher concentrations studied. We conclude that all spin traps examined acted as coronary vasodilators. Their negative chronotropic and inotropic effects were minimal in comparison and only manifest at the higher concentrations studied.
引用
收藏
页码:127 / 137
页数:11
相关论文
共 44 条
  • [1] IDENTIFICATION OF FREE-RADICALS IN MYOCARDIAL-ISCHEMIA REPERFUSION BY SPIN TRAPPING WITH NITRONE DMPO
    ARROYO, CM
    KRAMER, JH
    DICKENS, BF
    WEGLICKI, WB
    [J]. FEBS LETTERS, 1987, 221 (01): : 101 - 104
  • [2] SPIN TRAPPING OF OXYGEN AND CARBON-CENTERED FREE-RADICALS IN ISCHEMIC CANINE MYOCARDIUM
    ARROYO, CM
    KRAMER, JH
    LEIBOFF, RH
    MERGNER, GW
    DICKENS, BF
    WEGLICKI, WB
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1987, 3 (05) : 313 - 316
  • [3] PROTECTION FROM REPERFUSION INJURY IN THE ISOLATED RAT-HEART BY POSTISCHEMIC DEFEROXAMINE AND OXYPURINOL ADMINISTRATION
    BADYLAK, SF
    SIMMONS, A
    TUREK, J
    BABBS, CF
    [J]. CARDIOVASCULAR RESEARCH, 1987, 21 (07) : 500 - 506
  • [4] BATES JN, 1991, BASIC RES CARDIOL, V86, P17
  • [5] APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE
    BECKMAN, JS
    BECKMAN, TW
    CHEN, J
    MARSHALL, PA
    FREEMAN, BA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) : 1620 - 1624
  • [6] BLASIG IE, 1987, BIOMED BIOCHIM ACTA, V46, pS539
  • [7] VALUE OF THE QRS DURATION VERSUS THE SERUM DRUG LEVEL IN PREDICTING SEIZURES AND VENTRICULAR ARRHYTHMIAS AFTER AN ACUTE OVERDOSE OF TRICYCLIC ANTIDEPRESSANTS
    BOEHNERT, MT
    LOVEJOY, FH
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1985, 313 (08) : 474 - 479
  • [8] DEMONSTRATION OF FREE-RADICAL GENERATION IN STUNNED MYOCARDIUM OF INTACT DOGS WITH THE USE OF THE SPIN TRAP ALPHA-PHENYL N-TERT-BUTYL NITRONE
    BOLLI, R
    PATEL, BS
    JEROUDI, MO
    LAI, EK
    MCCAY, PB
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (02) : 476 - 485
  • [9] DIRECT EVIDENCE THAT OXYGEN-DERIVED FREE-RADICALS CONTRIBUTE TO POSTISCHEMIC MYOCARDIAL DYSFUNCTION IN THE INTACT DOG
    BOLLI, R
    JEROUDI, MO
    PATEL, BS
    DUBOSE, CM
    LAI, EK
    ROBERTS, R
    MCCAY, PB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (12) : 4695 - 4699
  • [10] Buettner G.R, 1982, SUPEROXIDE DISMUTASE, V2, P63