REVERSAL OF DOPAMINE-REFRACTORY SEPTIC SHOCK BY DIETHYLDITHIOCARBAMATE, AN INHIBITOR OF ENDOTHELIUM-DERIVED RELAXING FACTOR

被引:11
|
作者
BRONER, CW
SHENEP, JL
STOKES, DC
FAIRCLOUGH, D
HILDNER, WK
STORGION, SA
REHG, JE
机构
[1] ST JUDE CHILDRENS RES HOSP, DIV BIOSTAT, MEMPHIS, TN 38101 USA
[2] ST JUDE CHILDRENS RES HOSP, DIV COMPARAT MED, MEMPHIS, TN 38101 USA
[3] LEBONHEUR CHILDRENS HOSP & MED CTR, MEMPHIS, TN USA
[4] UNIV TENNESSEE, DEPT PEDIAT, DIV CRIT CARE, KNOXVILLE, TN 37996 USA
[5] ST JUDE CHILDRENS RES HOSP, DEPT INFECT DIS, MEMPHIS, TN 38101 USA
[6] ST JUDE CHILDRENS RES HOSP, DIV CARDIOPULM MED, MEMPHIS, TN 38101 USA
来源
JOURNAL OF INFECTIOUS DISEASES | 1993年 / 167卷 / 01期
关键词
D O I
10.1093/infdis/167.1.141
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Septic shock occurs when endotoxin and other bacterial substances induce the release of host products that act in concert to alter the circulation. Recently, investigators have speculated that endothelium-derived relaxing factor (EDRF), a potent endotoxin-inducible vasodilator, plays an important role in the pathogenesis of septic shock. Diethyldithiocarbamate (DTC), a copper chelator lacking intrinsic vasoactivity, inactivates EDRF. Intravenous DTC was compared with placebo and dopamine in 12 matched sets of 3 rabbits with induced Escherichia coli sepsis. Median levels of bacteremia and endotoxemia were similar in the 3 treatment groups. DTC-treated animals had higher mean arterial pressure and lower heart rates and blood lactate concentrations than either placebo- or dopamine-treated animals (P = .013, P < .001, and P = .001, respectively). These effects were independent of plasma catecholamine concentrations. DTC can reverse septic shock that is refractory to conventional therapy, and these results suggest that EDRF is an important mediator of septic shock.
引用
收藏
页码:141 / 147
页数:7
相关论文
共 50 条
  • [41] CALCIUM AND ACTIVATION OF THE RELEASE OF ENDOTHELIUM-DERIVED RELAXING FACTOR
    RUBANYI, GM
    VANHOUTTE, PM
    ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1988, 522 : 226 - 233
  • [42] ENDOTHELIUM-DERIVED RELAXING FACTOR MODULATES RENIN SECRETION
    VIDALRAGOUT, M
    LORENZ, RR
    BENTLEY, M
    ROMERO, JC
    VANHOUTTE, PM
    CLINICAL RESEARCH, 1988, 36 (03): : A546 - A546
  • [43] THE ENDOTHELIUM-DERIVED RELAXING FACTOR IN CARDIOVASCULAR-DISEASE
    LAHERA, V
    MEDICINA CLINICA, 1991, 96 (03): : 95 - 97
  • [44] ENDOTHELIUM-DERIVED RELAXING FACTOR - NITRIC-OXIDE
    BUSSE, R
    BIOLOGICAL CHEMISTRY HOPPE-SEYLER, 1991, 372 (04): : 242 - 242
  • [45] EDRF (ENDOTHELIUM-DERIVED RELAXING FACTOR) - ENDOGENOUS NITROVASODILATOR
    FORSTERMANN, U
    DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, 1988, 113 (31-32) : 1215 - 1217
  • [46] DETAILED EXAMINATION OF VASCULAR-LESIONS TRIGGERED BY AN INHIBITOR OF ENDOTHELIUM-DERIVED RELAXING FACTOR
    TAGAMI, M
    IKEDA, K
    NARA, Y
    FUJINO, H
    KUBOTA, A
    NUMANO, F
    YAMORI, Y
    LABORATORY INVESTIGATION, 1995, 72 (02) : 174 - 182
  • [47] ALPHA-2-ADRENOCEPTORS AND ENDOTHELIUM-DERIVED RELAXING FACTOR
    VANHOUTTE, PM
    MILLER, VM
    AMERICAN JOURNAL OF MEDICINE, 1989, 87 (3C): : S1 - S5
  • [48] ENDOTHELIUM-DERIVED RELAXING FACTOR IS IDENTIFIED AS NITRIC-OXIDE
    MONCADA, S
    HERMAN, AG
    VANHOUTTE, P
    TRENDS IN PHARMACOLOGICAL SCIENCES, 1987, 8 (10) : 365 - &
  • [50] ENDOTHELIUM-DERIVED RELAXING FACTOR AND THE VASCULAR REPLY TO SYSTEMIC HYPERTENSION
    KING, AJ
    MERCER, P
    TROY, JL
    BRENNER, BM
    JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 1991, 2 (06): : 1072 - 1077