EFFECT OF INTERFERON-GAMMA ON NITRIC-OXIDE HEMOGLOBIN PRODUCTION IN ENDOTOXIN-TREATED RATS AND ITS SYNERGISM WITH INTERLEUKIN-1 OR TUMOR-NECROSIS-FACTOR

被引:9
作者
KOSAKA, H
SAKAGUCHI, H
SAWAI, Y
KUMURA, E
SEIYAMA, A
CHEN, SS
SHIGA, T
机构
[1] Department of Physiology, Medical School, Osaka University, Suita, Osaka, 565
关键词
NITRIC OXIDE; HEMOGLOBIN; LIPOPOLYSACCHARIDE; INTERLEUKIN; 1; TUMOR NECROSIS FACTOR; INTERFERON-GAMMA;
D O I
10.1016/0024-3205(94)90020-5
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
We studied the in vivo effect of interferon-gamma (IFN-gamma) on nitric oxide (NO) generation. ESR spectra of nitric oxide hemoglobin (HbNO) appeared after a lag time of 2h in the blood of rats treated with Escherichia coli lipopolysaccharide (LPS). IFN-gamma enhanced LPS-induced HbNO formation in rats without modifying the time lag, although IFN-gamma alone did not include HbNO formation. The plasma nitrate concentration was approximately one order of magnitude higher than the HbNO concentration. On treatment with LPS alone, the amount of tumor necrosis factor (TNF) released decreased after 2 h. Simultaneous addition of IFN-gamma and LPS increased TNF release for at least 8 h. Interleukin 1 (IL-1) release was detected only at 2 h in both groups. We also investigated the in vivo interactions of these cytokines. TNF plus IL-1 induced the greatest HbNO generation, followed by TNF plus IFN-gamma, and then IL-1 plus IFN-gamma. These results suggest that increase of TNF release by IFN-gamma plays a key role in NO generation in LPS-treated rats.
引用
收藏
页码:1523 / 1529
页数:7
相关论文
共 31 条
[1]  
DING AH, 1988, J IMMUNOL, V141, P2407
[2]  
DRAPIER JC, 1988, J IMMUNOL, V140, P2829
[3]   INTERFERON-GAMMA AND TUMOR NECROSIS FACTOR INDUCE THE L-ARGININE-DEPENDENT CYTO-TOXIC EFFECTOR MECHANISM IN MURINE MACROPHAGES [J].
DRAPIER, JC ;
WIETZERBIN, J ;
HIBBS, JB .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (10) :1587-1592
[4]   ENDOTHELIUM-DERIVED RELAXING FACTOR RELEASE ON ACTIVATION OF NMDA RECEPTORS SUGGESTS ROLE AS INTERCELLULAR MESSENGER IN THE BRAIN [J].
GARTHWAITE, J ;
CHARLES, SL ;
CHESSWILLIAMS, R .
NATURE, 1988, 336 (6197) :385-388
[5]   CYTOKINES, ENDOTOXIN, AND GLUCOCORTICOIDS REGULATE THE EXPRESSION OF INDUCIBLE NITRIC-OXIDE SYNTHASE IN HEPATOCYTES [J].
GELLER, DA ;
NUSSLER, AK ;
DISILVIO, M ;
LOWENSTEIN, CJ ;
SHAPIRO, RA ;
WANG, SC ;
SIMMONS, RL ;
BILLIAR, TR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (02) :522-526
[6]   ANALYSIS OF NITRATE, NITRITE, AND [N-15]-LABELED NITRATE IN BIOLOGICAL-FLUIDS [J].
GREEN, LC ;
WAGNER, DA ;
GLOGOWSKI, J ;
SKIPPER, PL ;
WISHNOK, JS ;
TANNENBAUM, SR .
ANALYTICAL BIOCHEMISTRY, 1982, 126 (01) :131-138
[7]   ELECTRON-PARAMAGNETIC STUDIES OF NITRIC-OXIDE HEMOGLOBIN DERIVATIVES - ISOLATED SUBUNITS AND NITRIC-OXIDE HYBRIDS [J].
HENRY, Y ;
BANERJEE, R .
JOURNAL OF MOLECULAR BIOLOGY, 1973, 73 (04) :469-482
[8]   EVIDENCE FOR CYTOKINE-INDUCIBLE NITRIC-OXIDE SYNTHESIS FROM L-ARGININE IN PATIENTS RECEIVING INTERLEUKIN-2 THERAPY [J].
HIBBS, JB ;
WESTENFELDER, C ;
TAINTOR, R ;
VAVRIN, Z ;
KABLITZ, C ;
BARANOWSKI, RL ;
WARD, JH ;
MENLOVE, RL ;
MCMURRY, MP ;
KUSHNER, JP ;
SAMLOWSKI, WE .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (03) :867-877
[9]  
HORI K, 1987, CANCER RES, V47, P5868
[10]   ENDOTHELIUM-DERIVED RELAXING FACTOR PRODUCED AND RELEASED FROM ARTERY AND VEIN IS NITRIC-OXIDE [J].
IGNARRO, LJ ;
BUGA, GM ;
WOOD, KS ;
BYRNS, RE ;
CHAUDHURI, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (24) :9265-9269