Time course of inducible nitric oxide synthase activity following endotoxin administration in dogs

被引:55
作者
Preiser, JC
Zhang, HB
Vray, B
Hrabak, A
Vincent, JL [1 ]
机构
[1] Free Univ Brussels, Erasme Univ Hosp, Dept Intens Care, Brussels, Belgium
[2] Free Univ Brussels, Erasme Univ Hosp, Dept Immunol, Brussels, Belgium
来源
NITRIC OXIDE-BIOLOGY AND CHEMISTRY | 2001年 / 5卷 / 02期
关键词
septic shock; endotoxic shock; multiple organ dysfunction; bioassay; lipopolysaccharide;
D O I
10.1006/niox.2001.0342
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
An increased production of nitric oxide (NO) via the inducible isoform of NO synthase (iNOS) has been incriminated in the pathogenesis of septic shock. Since the time course of iNOS activity is not known during endotoxic shock in dogs, we measured iNOS activity, estimated by the rate of conversion of C-14-arginine to C-14-citrulline in the absence of calcium, in the heart, lung, liver, kidney, and gut at 1, 2, 3, 4, and 6 h after a bolus of Escherichia coli endotoxin (2 mg/kg, iv), in the dog. This model, including generous fluid administration, is associated with typical features of human septic shock, including low systemic vascular resistance, altered myocardial function and limited oxygen extraction capability. An increase in iNOS activity was observed at 4 h in the liver (0.24 vs 0.04 mU/mg/ min) and at 6 h in the heart (0.26 vs 0.09 mU/mg/ min). These findings may contribute to a better delineation of the involvement of NO in endotoxic shock, and to the evaluation of the therapeutic effects of NO inhibitors. (C) 2001 Academic Press.
引用
收藏
页码:208 / 211
页数:4
相关论文
共 14 条
[1]   Differential regulation of inducible nitric oxide synthase production in bovine and caprine macrophages [J].
Adler, H ;
Adler, B ;
Peveri, P ;
Werner, ER ;
Wachter, H ;
Peterhans, E ;
Jungi, TW .
JOURNAL OF INFECTIOUS DISEASES, 1996, 173 (04) :971-978
[2]   INTERLEUKIN-1 ACTIVATES SOLUBLE GUANYLATE-CYCLASE IN HUMAN VASCULAR SMOOTH-MUSCLE CELLS THROUGH A NOVEL NITRIC OXIDE-INDEPENDENT PATHWAY [J].
BEASLEY, D ;
MCGUIGGIN, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (01) :71-80
[3]   DIFFERENTIAL HEMODYNAMIC-EFFECTS OF L-NMMA IN ENDOTOXEMIC AND NORMAL DOGS [J].
COBB, JP ;
NATANSON, C ;
QUEZADO, ZMN ;
HOFFMAN, WD ;
KOEV, CA ;
BANKS, S ;
CORREA, R ;
LEVI, R ;
ELIN, RJ ;
HOSSEINI, JM ;
DANNER, RL .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1995, 268 (04) :H1634-H1642
[4]   LABORATORY MODELS OF SEPSIS AND SEPTIC SHOCK [J].
FINK, MP ;
HEARD, SO .
JOURNAL OF SURGICAL RESEARCH, 1990, 49 (02) :186-196
[5]   CARDIAC AND REGIONAL HEMODYNAMICS, INDUCIBLE NITRIC-OXIDE SYNTHASE (NOS) ACTIVITY, AND THE EFFECTS OF NOS INHIBITORS IN CONSCIOUS, ENDOTOXAEMIC RATS [J].
GARDINER, SM ;
KEMP, PA ;
MARCH, JE ;
BENNETT, T .
BRITISH JOURNAL OF PHARMACOLOGY, 1995, 116 (03) :2005-2016
[6]   REVERSAL OF ENDOTOXIN-MEDIATED SHOCK BY NG-METHYL-L-ARGININE, AN INHIBITOR OF NITRIC-OXIDE SYNTHESIS [J].
KILBOURN, RG ;
JUBRAN, A ;
GROSS, SS ;
GRIFFITH, OW ;
LEVI, R ;
ADAMS, J ;
LODATO, RF .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 172 (03) :1132-1138
[7]  
Numata M, 1998, J IMMUNOL, V160, P3031
[8]   IS ENDOTOXIN-INDUCED HYPOTENSION RELATED TO NITRIC-OXIDE FORMATION [J].
PREISER, JC ;
ZHANG, H ;
WACHEL, D ;
BOEYNAEMS, JM ;
BUURMAN, W ;
VINCENT, JL .
EUROPEAN SURGICAL RESEARCH, 1994, 26 (01) :10-18
[9]   INDUCTION AND POTENTIAL BIOLOGICAL RELEVANCE OF A CA2+-INDEPENDENT NITRIC-OXIDE SYNTHASE IN THE MYOCARDIUM [J].
SCHULZ, R ;
NAVA, E ;
MONCADA, S .
BRITISH JOURNAL OF PHARMACOLOGY, 1992, 105 (03) :575-580
[10]   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