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3-羟基邻氨基苯甲酸是色氨酸经吲哚胺2,3-双加氧酶途径产生的代谢产物之一,它通过增强血红素加氧酶-1的表达来抑制诱导型一氧化氮合酶的表达。

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.

作者信息

Oh Gi-Su, Pae Hyun-Ock, Choi Byung-Min, Chae Soo-Cheon, Lee Ho-Sub, Ryu Do-Gon, Chung Hun-Taeg

机构信息

Genomic Research Center for Immune Disorders, Department of Microbiology and Immunology, Wonkwang University School of Medicine, Iksan, Chonbuk 570-749, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2004 Aug 6;320(4):1156-62. doi: 10.1016/j.bbrc.2004.06.061.

Abstract

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.

摘要

诱导型一氧化氮(NO)合酶(iNOS)、血红素加氧酶(HO)-1和吲哚胺2,3-双加氧酶(IDO)在受到干扰素(IFN)-γ和脂多糖(LPS)刺激的小鼠巨噬细胞中同时表达。iNOS产生的NO抑制IDO表达,同时诱导HO-1表达。抗氧化剂3-羟基邻氨基苯甲酸(HA)是色氨酸经IDO途径的代谢产物之一,此前有报道称其可抑制iNOS表达。由于HO-1表达可抑制iNOS表达,我们研究了HA是否能通过影响经IFN-γ加LPS刺激的小鼠RAW 264.7巨噬细胞中的HO-1表达来抑制iNOS表达。用外源性HA处理可剂量依赖性地抑制iNOS表达,并同时增强HO-1表达。HA对iNOS表达的这种抑制作用可通过阻断HO-1活性而逆转,且已证实是由于HO-1产生的一氧化碳(CO)所致。此外,阻断iNOS活性或添加外源性CO均可进一步增强IDO表达和活性。这些结果首次表明,HA能够通过增强HO-1表达来抑制iNOS表达,从而导致IDO表达和活性进一步增加。

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