Chlorophyllin suppression of lipopolysaccharide-induced nitric oxide production in RAW 264.7 cells

被引:26
作者
Cho, KJ
Han, SH
Kim, BY
Hwang, SG
Park, KK
Yang, KH
Chung, AS
机构
[1] Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon 305701, South Korea
[2] Konkuk Univ, Coll Anim Husb, Anim Resources Res Ctr, Seoul 143701, South Korea
[3] Yonsei Univ, Coll Dent, Dept Oral Biol, Seoul 120752, South Korea
关键词
chlorophyllin; nitric oxide; lipopolysaccharide; NF-kappa B;
D O I
10.1006/taap.2000.8958
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chlorophyllin (CHL), a water-soluble derivative of chlorophyll, functions as an anticarcinogen and antioxidant. In the present study, we investigated the effect of CHL on nitric oxide production in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. Treatment with CHL inhibited nitric oxide production in the LPS-stimulated RAW 264.7 cells in a dose-related manner. Competitive RT-PCR analysis, using a DNA competitor as an internal standard, demonstrated that the treatment with 1, 10, and 50 mu M CHL decreased LPS-induced iNOS mRNA expression in a concentration-dependent manner. Since the expression of the iNOS gene is mainly regulated by NF-kappa B, we then examined the effects of CHL on the NF-kappa B DNA binding activity, using an electrophoretic mobility shift assay. CHL down-regulated the NF-kappa B DNA binding on its cognate recognition site at the concentrations just noted. Employing a transfection and reporter gene expression system with p(NF-kappa B)(3)-chloramphenicol acetyl transferase (CAT), the treatment of CHL produced a dose-dependent inhibition of CAT activity in RAW 264.7 cells. Furthermore, CHL partially restored LPS-decreased I kappa B alpha, an inhibitory protein against NF-kappa B activation, in the cytosolic extract from the LPS-treated cells determined by immunoblot analysis. CHL also protected the hydroxyl radical-induced cytotoxicity in RAW 264.7 cells, indicating its antioxidant effect. These results suggest that CHL suppresses the nitric oxide production and iNOS mRNA expression mediated by the inhibition of NF-kappa B activation, and its action mechanism may be based on its antioxidant effect. (C) 2000 Academic Press.
引用
收藏
页码:120 / 127
页数:8
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