Chloroquine inhibits inducible nitric oxide synthase expression in murine peritoneal macrophages

被引:13
作者
Park, YC
Pae, HO
Yoo, JC
Choi, BM
Jue, DM
Chung, HT [1 ]
机构
[1] Wonkwang Univ, Sch Med, Dept Microbiol & Immunol, Iksan 570749, Chonbuk, South Korea
[2] Wonkwang Univ, Sch Med, Med Resources Res Ctr, Iksan 570749, Chonbuk, South Korea
[3] Catholic Univ, Coll Med, Dept Biochem, Seoul, South Korea
来源
PHARMACOLOGY & TOXICOLOGY | 1999年 / 85卷 / 04期
关键词
D O I
10.1111/j.1600-0773.1999.tb00090.x
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Induction of inducible nitric oxide synthase in vivo or in vitro in response to stimuli is only temporary However, chronic localized expression of inducible nitric oxide synthase in certain organs has been associated with the development of autoimmune diseases or chronic inflammatory diseases. Chloroquine is being used as an antiinflammatory drug, and its inhibitory effect on the synthesis of pro-inflammatory cytokines, such as tumour necrosis factor-cc and interferon-gamma, has been reported. In this study, we examined whether chloroquine could inhibit nitric oxide synthesis in murine peritoneal macrophages stimulated with interferon-gamma and lipopolysaccharide. Although prolonged incubation of cells with high concentrations of chloroquine showed some cytotoxicity, the drug itself was not cytotoxic when macrophages were preincubated with chloroquine for 2 hr, washed and stimulated with interferon-gamma and lipopolysaccharide in the absence of chloroquine for another 48 hr. The nitric oxide production from stimulated macrophages was markedly reduced by chloroquine in a dose-dependent manner and induction of inducible nitric oxide synthase mRNA was also suppressed by chloroquine pretreatment. These results show that chloroquine inhibits the induction of inducible nitric oxide synthase from interferon-gamma and lipopolysaccharide-stimulated macrophages, thereby reducing nitric oxide synthesis.
引用
收藏
页码:188 / 191
页数:4
相关论文
共 15 条
[1]
NITRIC-OXIDE SYNTHESIZED FROM L-ARGININE REGULATES VASCULAR TONE IN THE CORONARY CIRCULATION OF THE RABBIT [J].
AMEZCUA, JL ;
PALMER, RMJ ;
DESOUZA, BM ;
MONCADA, S .
BRITISH JOURNAL OF PHARMACOLOGY, 1989, 97 (04) :1119-1124
[2]
AUGUSTIJNS P, 1992, EUR J CLIN PHARMACOL, V42, P429
[3]
Inhibition of macrophage nitric oxide production by tetrahydrocannabinol in vivo and in vitro [J].
Coffey, RG ;
Snella, E ;
Johnson, K ;
Pross, S .
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY, 1996, 18 (12) :749-752
[4]
CORRECTION OF ENDOTHELIAL DYSFUNCTION IN CORONARY MICROCIRCULATION OF HYPERCHOLESTEROLEMIC PATIENTS BY L-ARGININE [J].
DREXLER, H ;
ZEIHER, AM ;
MEINZER, K ;
JUST, H .
LANCET, 1991, 338 (8782-3) :1546-1550
[5]
PHARMACOKINETICS OF CHLOROQUINE IN THAIS - PLASMA AND RED-CELL CONCENTRATIONS FOLLOWING AN INTRAVENOUS-INFUSION TO HEALTHY-SUBJECTS AND PATIENTS WITH PLASMODIUM-VIVAX MALARIA [J].
EDWARDS, G ;
LOOAREESUWAN, S ;
DAVIES, AJ ;
WATTANAGOON, Y ;
PHILLIPS, RE ;
WARRELL, DA .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1988, 25 (04) :477-485
[6]
Human and rat neutrophils constitutively express neural nitric oxide synthase mRNA [J].
Greenberg, SS ;
Ouyang, J ;
Zhao, XF ;
Giles, TD .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 1998, 2 (03) :203-212
[7]
NITRIC-OXIDE SYNTHASES IN MAMMALS [J].
KNOWLES, RG ;
MONCADA, S .
BIOCHEMICAL JOURNAL, 1994, 298 :249-258
[8]
Nitric oxide synthases: Which, where, how, and why? [J].
Michel, T ;
Feron, O .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (09) :2146-2152
[9]
NITRIC-OXIDE SYNTHASES - ROLES, TOLLS, AND CONTROLS [J].
NATHAN, C ;
XIE, QW .
CELL, 1994, 78 (06) :915-918
[10]
CHLOROQUINE INDUCES HUMAN MACROPHAGE KILLING OF HISTOPLASMA-CAPSULATUM BY LIMITING THE AVAILABILITY OF INTRACELLULAR IRON AND IS THERAPEUTIC IN A MURINE MODEL OF HISTOPLASMOSIS [J].
NEWMAN, SL ;
GOOTEE, L ;
BRUNNER, G ;
DEEPE, GS .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (04) :1422-1429