3-hydroxyanthranilic acid, one of metabolites of tryptophan via indoleamine 2,3-dioxygenase pathway, suppresses inducible nitric oxide synthase expression by enhancing heme oxygenase-1 expression

被引:79
作者
Oh, GS
Pae, HO
Choi, BM
Chae, SC
Lee, HS
Ryu, DG
Chung, HT [1 ]
机构
[1] Wonkwang Univ, Sch Med, Dept Microbiol & Immunol, Gentom Res Ctr Immune Disorders, Chonbuk 570749, South Korea
[2] Wonkwang Univ, Dept Herbal Resources, Prof Grad Sch Oriental Med, Chonbuk 570749, South Korea
[3] Wonkwang Univ, Hangbang Brain Dis Res Ctr, Chonbuk 570749, South Korea
[4] Wonkwang Univ, Sch Oriental Med, Dept Physiol, Chonbuk 570749, South Korea
关键词
3-hydroxyanthranilic acid; inducible nitric oxide synthase; heme oxygenase-1; indoleamine; 2.3-dioxygenase; nitric oxide; carbon monoxide; macrophages;
D O I
10.1016/j.bbrc.2004.06.061
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
Inducible nitric oxide (NO) synthase (iNOS). heme oxygenase (HO)-1, and indoleamine 2,3-dioxygenase (IDO) are simultaneously expressed in murine macrophages stimulated with interferon (IFN)-gamma and lipopolysaccharide (LPS). NO produced by iNOS suppresses IDO expression and also induces HO-1 expression. The antioxidant 3-hydroxyanthranilic acid (HA), one of metabolites of tryptophan via IDO pathway, has been previously reported to suppress iNOS expression. Because HO-1 expression can suppress iNOS expression, we investigated whether HA could suppress iNOS expression by affecting HO-1 expression in murine RAW 264.7 macrophages stimulated with IFN-gamma plus LPS. Treatment with exogenous HA dose-dependently suppressed iNOS expression and coincidently enhanced HO-1 expression. This suppressive effect of HA on iNOS expression was reversed by blocking HO-1 activity, and proven to be due to carbon monoxide (CO) produced by HO-1. In addition, either blocking of iNOS activity or addition of exogenous CO further enhanced IDO expression and activity. These results show for the first time that HA is able to suppress iNOS expression by enhancing HO-1 expression, thereby resulting in further increases in IDO expression and activity. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1156 / 1162
页数:7
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