Inhibition of UVA irradiation-modulated signaling pathways by rutaecarpine, a quinazolinocarboline alkaloid, in human keratinocytes

被引:24
作者
Beak, SM
Paek, SH
Jahng, Y
Lee, YS
Kim, JA [1 ]
机构
[1] Yeungnam Univ, Coll Pharm, Kyongsan 712749, South Korea
[2] Duksung Womens Univ, Coll Pharm, Seoul 132714, South Korea
基金
新加坡国家研究基金会;
关键词
rutaecarpine; reactive oxygen species; matrix metalloproteinase; HaCaT human keratinocyte;
D O I
10.1016/j.ejphar.2004.07.065
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Matrix metalloproteinases (MMPs), a key component in photoaging of the skin due to exposure to ultraviolet A, appear to be increased by ultraviolet A irradiation-associated generation of reactive oxygen species. In this study, we investigated the effects of synthetic rutaecarpine, which is also found in Evodia rutaecarpa, on the ultraviolet A-induced changes in the expression of gelatinases: matrix metalloproteinase (MMP)-2 and MMP-9 using HaCaT human keratinocytes as a model cellular system. Ultraviolet A irradiation of HaCaT cells increased the gelatinolytic activities of MMP-2 and MMP-9, which was significantly suppressed by the pretreatment with rutaecarpine. In addition, rutaecarpine significantly suppressed the ultraviolet A-induced enhanced expression of MMP-2 and MMP-9 proteins and mRNAs. Rutaecarpine also inhibited the H2O2-induced increase in the expression of MMP-2 and MMP-9. Furthermore, rutaecarpine decreased the ultraviolet A-induced increased generation of reactive oxygen species. Taken together, these results suggest that rutaecarpine inhibited ultraviolet A-induced reactive oxygen species generation, resulting in the enhanced expression of MMP-2 and MMP-9 in human skin cells. These results further suggest that ruetaecarpine may be useful in the prevention of ultraviolet A-induced photoaging. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:19 / 25
页数:7
相关论文
共 31 条
[11]  
Hanson KM, 2002, PHOTOCHEM PHOTOBIOL, V76, P57, DOI 10.1562/0031-8655(2002)076<0057:OAQOUI>2.0.CO
[12]  
2
[13]  
HERRON GS, 1986, J BIOL CHEM, V261, P2814
[14]   Matrix metalloproteinases [J].
Johnson, LL ;
Dyer, R ;
Hupe, DJ .
CURRENT OPINION IN CHEMICAL BIOLOGY, 1998, 2 (04) :466-471
[15]   Differential regulation of MMP-2 and MMP-9 gelatinases in cultured human keratinocytes [J].
Kobayashi, T ;
Hattori, S ;
Nagai, Y ;
Tajima, S ;
Nishikawa, T .
DERMATOLOGY, 1998, 197 (01) :1-5
[16]   DNA damage, death receptor activation and reactive oxygen species contribute to ultraviolet radiation-induced apoptosis in an essential and independent way [J].
Kulms, D ;
Zeise, E ;
Pöppelmann, B ;
Schwarz, T .
ONCOGENE, 2002, 21 (38) :5844-5851
[17]  
Lee SH, 2001, HETEROCYCLES, V55, P1555
[18]   Inhibition of ultraviolet-A-modulated signaling pathways by asiatic acid and ursolic acid in HaCaT human keratinocytes [J].
Lee, YS ;
Jin, DQ ;
Beak, SM ;
Lee, ES ;
Kim, JA .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2003, 476 (03) :173-178
[19]   DETECTION OF HYDROGEN-PEROXIDE AND HYDROXYL RADICALS IN MURINE SKIN FIBROBLASTS UNDER UVB IRRADIATION [J].
MASAKI, H ;
ATSUMI, T ;
SAKURAI, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 206 (02) :474-479
[20]   A new class of COX-2 inhibitor, rutaecarpine from Evodia rutaecarpa [J].
Moon, TC ;
Murakami, M ;
Kudo, I ;
Son, KH ;
Kim, HP ;
Kang, SS ;
Chang, HW .
INFLAMMATION RESEARCH, 1999, 48 (12) :621-625