THE INFLUENCE OF ANTIOXIDANTS AND CYCLOHEXIMIDE ON THE LEVEL OF NITRIC-OXIDE IN THE LIVERS OF MICE IN-VIVO

被引:31
作者
MIKOYAN, VD [1 ]
VOEVODSKAYA, NV [1 ]
KUBRINA, LN [1 ]
MALENKOVA, IV [1 ]
VANIN, AF [1 ]
机构
[1] RUSSIAN ACAD SCI,INST CHEM PHYS,MOSCOW 117977,RUSSIA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 1995年 / 1269卷 / 01期
关键词
ACTIVE OXYGEN SPECIES; ANTIOXIDANT; INDUCIBLE NO SYNTHASE; NITRIC OXIDE;
D O I
10.1016/0167-4889(95)00092-7
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
When injected into mice prior to the NO generation increase induced with lipopolysaccharide (LPS) from Escherichia coli, exogenous antioxidants diethyldithiocarbamate (DETC) or phenazan (sodium 3.5-di-tert-butyl-4-oxiphenylpropionate) as well as the inhibitor of protein biosynthesis, cycloheximide (CHI) attenuated the NO production in mouse liver in vivo. These data demonstrated the key role of free radicals, which were likely, active oxygen species, in the synthesis of inducible NO-synthase (iNOS) responsible for the NO production in this organ. Similar effects of phenazan and CHI were observed in livers of mice treated with gamma-irradiation or LPS + Fe2(+)-citrate, which suggested that these treatments also:induced INOS synthesis through initiating the action of active oxygen species. The rate of NO synthesis was estimated by accumulation of paramagnetic mononitrosyl iron complexes with DETC (MNIC-DETC) detected using the EPR method. The formation of MNIC-DETC complexes was found in the brain of mice pre-treated with LPS + Fe2+-citrate which seemed to be due to iNOS synthesis stimulated by this treatment.
引用
收藏
页码:19 / 24
页数:6
相关论文
共 20 条
[1]   OXIDATIVE STRESS INDUCES NF-KAPPA-B DNA-BINDING AND INDUCIBLE NOS MESSENGER-RNA IN HUMAN EPITHELIAL-CELLS [J].
ADCOCK, IM ;
BROWN, CR ;
KWON, O ;
BARNES, PJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 199 (03) :1518-1524
[2]   NOS MESSENGER-RNA IN THE PARAVENTRICULAR NUCLEUS OF YOUNG AND OLD RATS AFTER IMMOBILIZATION STRESS [J].
CALZA, L ;
GIARDINO, L ;
CECCATELLI, S .
NEUROREPORT, 1993, 4 (06) :627-630
[3]   PYRROLIDINE DITHIOCARBAMATE DIFFERENTIALLY AFFECTS INTERLEUKIN 1-BETA-INDUCED AND CAMP-INDUCED NITRIC-OXIDE SYNTHASE EXPRESSION IN RAT RENAL MESANGIAL CELLS [J].
EBERHARDT, W ;
KUNZ, D ;
PFEILSCHIFTER, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 200 (01) :163-170
[4]   ELECTRON SPIN RESONANCE OF BIS(NN-DIETHYLTHIOCARBAMATO)MITROSYLIRON [J].
GOODMAN, BA ;
RAYNOR, JB ;
SYMONS, MCR .
JOURNAL OF THE CHEMICAL SOCIETY A -INORGANIC PHYSICAL THEORETICAL, 1969, (17) :2572-&
[5]  
HEIKKILA RE, 1976, J BIOL CHEM, V251, P2182
[6]   THE REACTION OF NO WITH SUPEROXIDE [J].
HUIE, RE ;
PADMAJA, S .
FREE RADICAL RESEARCH COMMUNICATIONS, 1993, 18 (04) :195-199
[7]   DIFFERENTIAL INDUCTION OF BRAIN, LUNG AND LIVER NITRIC-OXIDE SYNTHASE BY ENDOTOXIN IN THE RAT [J].
KNOWLES, RG ;
MERRETT, M ;
SALTER, M ;
MONCADA, S .
BIOCHEMICAL JOURNAL, 1990, 270 (03) :833-836
[8]   INVIVO EXPRESSION OF INDUCIBLE NITRIC-OXIDE SYNTHASE IN EXPERIMENTALLY INDUCED NEUROLOGIC DISEASES [J].
KOPROWSKI, H ;
ZHENG, YM ;
HEBERKATZ, E ;
FRASER, N ;
RORKE, L ;
FU, ZF ;
HANLON, C ;
DIETZSCHOLD, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (07) :3024-3027
[9]   IRON POTENTIATES BACTERIAL LIPOPOLYSACCHARIDE-INDUCED NITRIC-OXIDE FORMATION IN ANIMAL ORGANS [J].
KUBRINA, LN ;
MIKOYAN, VD ;
MORDVINTCEV, PI ;
VANIN, AF .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1176 (03) :240-244
[10]   EPR EVIDENCE FOR NITRIC-OXIDE PRODUCTION FROM GUANIDINO NITROGENS OF L-ARGININE IN ANIMAL-TISSUES INVIVO [J].
KUBRINA, LN ;
CALDWELL, WS ;
MORDVINTCEV, PI ;
MALENKOVA, IV ;
VANIN, AF .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1099 (03) :233-237