Nitrosyl heme production compared in endotoxemic and hemorrhagic shock

被引:18
作者
Davies, NA
Brealey, DA
Stidwill, R
Singer, M
Svistunenko, DA
Cooper, CE [1 ]
机构
[1] Univ Essex, Dept Biol Sci, Colchester CO4 3SQ, Essex, England
[2] UCL, Bloomsbury Inst Intens Care Med, Wolfson Inst Biomed Res, London, England
[3] UCL, Dept Med, London, England
基金
英国惠康基金;
关键词
sepsis; hemorrhage; endotoxin; nitric oxide; electron paramagnetic resonance; nitrosyl hemoglobin; cytochrome P450; mitochondria; free radicals;
D O I
10.1016/j.freeradbiomed.2004.09.026
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
We compared nitric oxide production and nitrosyl hemoglobin steady state concentrations during the early phases of endotoxemic and hemorrhagic shock of equivalent severity. Sprague Dawley rats were randomly assigned to (1) sham-operated control, (2) hemorrhage, and (3) intravenous endotoxin. Electron paramagnetic resonance spectroscopy was used to measure NO in the vasculature (binding to hemoglobin) and in the liver (binding to cytochrome P450). Despite similar changes in cardiorespiratory variables and identical microvascular pO(2), nitrosyl hemoglobin concentrations were significantly higher in endotoxemic rats than in rats in hemorrhagic shock, suggesting increased rates of NO production. A substantial venous minus arterial concentration gradient was observed for nitrosyl hemoglobin. This increased in line with the plasma total nitrite + nitrate concentration. Nitrosyl hemoglobin formation is likely to occur predominantly in the venous pool, suggesting that removal of NO from hemoglobin in the presence of oxygen may be faster than previously thought. In the liver, an increase in intracellular heme-NO complexes was detected in endotoxemic rats compared with rats in hemorrhagic shock; this was associated with increased reduction of the mitochondrial respiratory chain and is suggestive of NO inhibition of mitochondrial respiration. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:41 / 49
页数:9
相关论文
共 51 条
[41]   Comparative study of tyrosine radicals in hemoglobin and myoglobins treated with hydrogen peroxide [J].
Svistunenko, DA ;
Dunne, J ;
Fryer, M ;
Nicholls, P ;
Reeder, BJ ;
Wilson, MT ;
Bigotti, MG ;
Cutruzzolà, F ;
Cooper, CE .
BIOPHYSICAL JOURNAL, 2002, 83 (05) :2845-2855
[42]   NITRIC OXIDE-MEDIATED HYPOREACTIVITY TO NORADRENALINE PRECEDES THE INDUCTION OF NITRIC-OXIDE SYNTHASE IN ENDOTOXIN-SHOCK [J].
SZABO, C ;
MITCHELL, JA ;
THIEMERMANN, C ;
VANE, JR .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 108 (03) :786-792
[43]   PLATELET-ACTIVATING-FACTOR CONTRIBUTES TO THE INDUCTION OF NITRIC-OXIDE SYNTHASE BY BACTERIAL LIPOPOLYSACCHARIDE [J].
SZABO, C ;
WU, CC ;
MITCHELL, JA ;
GROSS, SS ;
THIEMERMANN, C ;
VANE, JR .
CIRCULATION RESEARCH, 1993, 73 (06) :991-999
[44]   VASCULAR HYPOREACTIVITY TO VASOCONSTRICTOR AGENTS AND HEMODYNAMIC DECOMPENSATION IN HEMORRHAGIC-SHOCK IS MEDIATED BY NITRIC-OXIDE [J].
THIEMERMANN, C ;
SZABO, C ;
MITCHELL, JA ;
VANE, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (01) :267-271
[45]   The biological lifetime of nitric oxide:: Implications for the perivascular dynamics of NO and O2 [J].
Thomas, DD ;
Liu, ZP ;
Kantrow, SP ;
Lancaster, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (01) :355-360
[46]  
VANDERKOOI JM, 1987, J BIOL CHEM, V262, P5476
[47]  
WANG Q, 1991, LIFE SCI PHARM LETT, V49, P55
[48]   Selective inhibition of the activity of inducible nitric oxide synthase prevents the circulatory failure, but not the organ injury/dysfunction, caused by endotoxin [J].
Wray, GM ;
Millar, CG ;
Hinds, CJ ;
Thiemermann, C .
SHOCK, 1998, 9 (05) :329-335
[49]   Measurements of nitric oxide on the heme iron and β-93 thiol of human hemoglobin during cycles of oxygenation and deoxygenation [J].
Xu, XL ;
Cho, M ;
Spencer, NY ;
Patel, N ;
Huang, Z ;
Shields, H ;
King, SB ;
Gladwin, MT ;
Hogg, N ;
Kim-Shapiro, DB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (20) :11303-11308
[50]   Significance of NO in hemorrhage-induced hemodynamic alterations, organ injury, and mortality in rats [J].
Yao, YM ;
Bahrami, S ;
Lichtfried, G ;
Redl, H ;
Schlag, G .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1996, 270 (05) :H1616-H1623