Anti-tumor necrosis factor-alpha improves myocardial recovery after ischemia and reperfusion

被引:134
作者
Gurevitch, J
Frolkis, I
Yuhas, Y
LifschitzMercer, B
Berger, E
Paz, Y
Matsa, M
Kramer, A
Mohr, R
机构
[1] ELIAS SOURASKY TEL AVIV MED CTR,INST PATHOL,DIAGNOST & RES CANC CTR,IL-64239 TEL AVIV,ISRAEL
[2] FELSENSTEIN MED RES CTR,PETAH TIQWA,ISRAEL
关键词
D O I
10.1016/S0735-1097(97)00328-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. This study sought to assess the importance of locally released or paracrine myocardial tumor necrosis factor alpha (TNF-alpha) in the evolution of postischemic myocardial dysfunction and to use immunohistochemical studies to localize TNF-alpha within the myocardium. Background. TNF alpha is implicated as a systemic mediator in the development of myocardial ischemia-reperfusion injury by promoting leukocyte myocardial infiltration, and it has been shown to originate from noncardiac peripheral mononuclear cells. We have recently documented in a blood-free environment the release of TNF-alpha from the ischemic-reperfused myocardium. Methods. Isolated rat hearts undergoing 1 h of global cardioplegia-induced ischemia and 30 min of reperfusion mere investigated with use of the modified Langendorff model. Hearts were randomly divided into three subgroups: group A, control group; and groups B and C, isolated hearts receiving cardioplegic solution containing monoclonal hamster antimurine TNF-alpha antibodies (group B) or hamster IgG (group C). Results. Significant amounts of TNF-alpha were detected in group A and group C effluent on 1 min of reperfusion (752 +/- 212 and 958 +/- 409 pmol/ml, respectively). However, in group B, TNF-alpha,vas below detectable levels. In this group, postischemic left ventricular peak systolic pressures, first derivative of the rise in left ventricular pressure (dP/dt(max)), pressure-time integral, coronary flow and O-2 consumption improved (analysis of variance [ANOVA] p < 0.0001 for all variables) compared with values in groups A and C; creatine kinase levels decreased (p < 0.005); and myocardial structure was preserved. Immunohistochemical staining localized TNF-alpha to cardiac myocytes and to endothelial cells. Conclusions. Anti-TNF-alpha neutralizes local TNF-alpha release from cardiac myocytes after ischemia and improves myocardial recovery during reperfusion, indicating that postischemic paracrine TNF-alpha release plays an active role in myocardial dysfunction. (C) 1997 by the American College of Cardiology.
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收藏
页码:1554 / 1561
页数:8
相关论文
共 36 条
  • [1] ARBUSTINI E, 1991, AM J PATHOL, V139, P709
  • [2] CAPUTI A P, 1992, Pharmacological Research, V26, P150, DOI 10.1016/1043-6618(92)90640-W
  • [3] ENDOTOXIN-INDUCED SERUM FACTOR THAT CAUSES NECROSIS OF TUMORS
    CARSWELL, EA
    OLD, LJ
    KASSEL, RL
    GREEN, S
    FIORE, N
    WILLIAMSON, B
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (09) : 3666 - 3670
  • [4] DINERMAN JL, 1991, J AM COLL CARDIOL, V17, P1445
  • [6] NEGATIVE INOTROPIC EFFECTS OF CYTOKINES ON THE HEART MEDIATED BY NITRIC-OXIDE
    FINKEL, MS
    ODDIS, CV
    JACOB, TD
    WATKINS, SC
    HATTLER, BG
    SIMMONS, RL
    [J]. SCIENCE, 1992, 257 (5068) : 387 - 389
  • [7] INHIBITION OF TUMOR-NECROSIS-FACTOR PREVENTS MYOCARDIAL DYSFUNCTION DURING BURN SHOCK
    GIROIR, BP
    HORTON, JW
    WHITE, DJ
    MCINTYRE, KL
    LIN, CQ
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (01): : H118 - H124
  • [8] Tumor necrosis factor-alpha is released from the isolated heart undergoing ischemia and reperfusion
    Gurevitch, J
    Frolkis, I
    Yuhas, Y
    Paz, Y
    Matsa, M
    Mohr, R
    Yakirevich, V
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1996, 28 (01) : 247 - 252
  • [9] HERSKOWITZ A, 1995, AM J PATHOL, V146, P419
  • [10] NEUTROPHIL ADHERENCE TO RAT CARDIAC MYOCYTE BY PROINFLAMMATORY CYTOKINES
    IKEDA, U
    IKEDA, M
    KANO, S
    SHIMADA, K
    [J]. JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1994, 23 (04) : 647 - 652