Iron attenuates nitric oxide level and iNOS expression in endotoxin-treated mice

被引:20
作者
Komarov, AM
Mattson, DL
Mak, IT
Weglicki, WB
机构
[1] George Washington Univ, Med Ctr, Div Expt Med, Washington, DC 20037 USA
[2] George Washington Univ, Med Ctr, Dept Physiol, Washington, DC 20037 USA
[3] Med Coll Wisconsin, Dept Physiol, Milwaukee, WI 53226 USA
来源
FEBS LETTERS | 1998年 / 424卷 / 03期
关键词
septic shock; nitric oxide; iron; inducible nitric oxide synthase; nitrosyl iron complex; spin trapping;
D O I
10.1016/S0014-5793(98)00181-1
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 effect of exogenous Fe-citrate complex (Fe doses of 120 and 240 mu mol/kg) on nitric oxide (NO) production in vivo has been studied in blood and liver tissue of endotoxin-treated mice, Fe-citrate complex was administered to mice subcutaneously at the same time with intravenous injection of Escherichia coli lipopolysaccharide (LPS), Iron-dependent decrease in NO2-/NO3- and nitrosyl hemoglobin levels in blood of animals was detected at 6 h after LPS administration, suggesting systemic attenuation of NO generation, NO production in the liver tissue of LPS-treated mice was decreased after Fe administration judging from the amount of mononitrosyl-iron complexes formed in the tissue by diethyldithiocarbamate. The iNOS protein determination in the liver tissue of LPS-treated mice demonstrated iron-dependent inhibition of iNOS expression, We have found previously that exogenous iron does not affect systemic NO level when it is given at 6 h after LPS injection, i.e. after iNOS expression, This is a first report demonstrating iron-dependent iNOS down-regulation in endotoxin-treated mice, (C) 1998 Federation of European Biochemical Societies.
引用
收藏
页码:253 / 256
页数:4
相关论文
共 24 条
[1]   A RAPID METHOD FOR THE ASSAY OF NITRATE IN URINE USING THE NITRATE REDUCTASE ENZYME OF ESCHERICHIA-COLI [J].
BARTHOLOMEW, B .
FOOD AND CHEMICAL TOXICOLOGY, 1984, 22 (07) :541-543
[2]  
Granger DL, 1996, METHOD ENZYMOL, V268, P142
[3]   Molecular control of vertebrate iron metabolism: mRNA-based regulatory circuits operated by iron, nitric oxide, and oxidative stress [J].
Hentze, MW ;
Kuhn, LC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (16) :8175-8182
[4]   INACTIVATION OF BACTERIAL EXOTOXINS AND ENDOTOXIN BY IRON - INVITRO STUDIES [J].
JANOFF, A ;
ZWEIFACH, BW .
JOURNAL OF EXPERIMENTAL MEDICINE, 1960, 112 (01) :23-34
[5]  
Kanner J, 1996, METHOD ENZYMOL, V269, P218
[6]   Iron chelates bind nitric oxide and decrease mortality in an experimental model of septic shock [J].
Kazmierski, WM ;
Wolberg, G ;
Wilson, JG ;
Smith, SR ;
Williams, DS ;
Thorp, HH ;
Molina, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (17) :9138-9141
[7]   LOSS AND DEGRADATION OF ENZYME-BOUND HEME INDUCED BY CELLULAR NITRIC-OXIDE SYNTHESIS [J].
KIM, YM ;
BERGONIA, HA ;
MULLER, C ;
PITT, BR ;
WATKINS, WD ;
LANCASTER, JR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (11) :5710-5713
[8]   Iron potentiates nitric oxide scavenging by dithiocarbamates in tissue of septic shock mice [J].
Komarov, AM ;
Mak, IT ;
Weglicki, WB .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1997, 1361 (03) :229-234
[9]   DETECTION OF NITRIC-OXIDE PRODUCTION IN MICE BY SPIN-TRAPPING ELECTRON-PARAMAGNETIC-RESONANCE SPECTROSCOPY [J].
KOMAROV, AM ;
LAI, CS .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1995, 1272 (01) :29-36
[10]   ALTERED RESPONSES TO BACTERIAL-INFECTION AND ENDOTOXIC-SHOCK IN MICE LACKING INDUCIBLE NITRIC-OXIDE SYNTHASE [J].
MACMICKING, JD ;
NATHAN, C ;
HOM, G ;
CHARTRAIN, N ;
FLETCHER, DS ;
TRUMBAUER, M ;
STEVENS, K ;
XIE, QW ;
SOKOL, K ;
HUTCHINSON, N ;
CHEN, H ;
MUDGETT, JS .
CELL, 1995, 81 (04) :641-650