Dual inhibitory effects of furonaphthoquinone compound on enzyme activity and lipopolysaccharide-induced expression of cyclooxygenase-2 in macrophages

被引:6
作者
Ahn, KY
Kim, BH [1 ]
Lee, YR
Hwang, DH
Chung, EY
Min, KR
Kim, YS
机构
[1] Chungbuk Natl Univ, Coll Pharm, Cheongju 361763, South Korea
[2] Chungbuk Natl Univ, Res Ctr Bioresource & Hlth, Cheongju 361763, South Korea
[3] Yeungnam Univ, Sch Chem Engn & Technol, Kyongsan 712749, South Korea
关键词
furonaphthoquinone compound; prostaglandin E-2; cyclooxygenase-2; nuclear factor-kappa B;
D O I
10.1016/j.bbrc.2005.08.059
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
2-Methyl-2-(2-methylpropenyl)-2,3-dihydronaphtho[2,3-b]furan-4,9-dione (NFD-37) is a synthetic furonaphthoquinone compound. In the present study, the NFD-37 compound was found to inhibit prostaglandin (PG) E-2 production in lipopolysaccharide (LPS)-stimulated macrophages RAW 264.7. NFD-37 compound exhibited a preferred inhibition on enzyme activity of cyclooxygenase (COX)-2 over COX-1. Further, NFD-37 compound attenuated LPS-induced synthesis of both mRNA and protein of COX-2, and suppressed LPS-induced COX-2 promoter activity in the macrophages, indicating that the furonaphthoquinone compound could down-regulate LPS-induced COX-2 expression at the transcription level. Even though COX-2 promoter behaves as a sophisticated biosensor for host defense, nuclear factor (NF)-kappa B activation has been evidenced to play a major mechanism for LPS-induced COX-2 expression in macrophages. NFD-37 compound exhibited a dose-dependent inhibitory effect on LPS-induced phosphorylation of inhibitory kappa B alpha (I kappa B alpha) protein, and subsequently inhibited I kappa B alpha degradation, DNA binding activity of NF-kappa B complex as well as NF-kappa B transcriptional activity in macrophages RAW 264.7. In another experiment, NFD-37 compound inhibited both COX-2 promoter activity and GST-I kappa B alpha phosphorylation elicited by an expression vector encoding I kappa B kinase beta. Taken together, NFD-37 compound inhibited enzyme activity of COX-2 but also suppressed COX-2 expression depending on NF-kappa B activation, and thus could provide an invaluable tool to investigate pharmacological potential in the excess PG-related disorders. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:93 / 99
页数:7
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