Acetylated Resveratrol and Oxyresveratrol Suppress UVB-Induced MMP-1 Expression in Human Dermal Fibroblasts

被引:13
作者
Lee, Jae-Eun [1 ]
Oh, Jijeong [1 ]
Song, Daeun [1 ]
Lee, Mijeong [1 ]
Hahn, Dongyup [1 ,2 ]
Boo, Yong Chool [3 ]
Kang, Nam Joo [1 ,2 ]
机构
[1] Kyungpook Natl Univ, Sch Food Sci & Biotechnol, Daegu 41566, South Korea
[2] Kyungpook Natl Univ, Dept Integrat Biol, Daegu 41566, South Korea
[3] Kyungpook Natl Univ, Sch Med, BK21 Plus KNU Biomed Convergence Program, Dept Mol Med,Cell & Matrix Res Inst, Daegu 41944, South Korea
关键词
resveratrol; oxyresveratrol; acetylated derivative; matrix metalloproteinase-1; type I collagen; ultraviolet B; skin aging; MATRIX METALLOPROTEINASES; HUMAN KERATINOCYTES; OXIDATIVE STRESS; ANTIOXIDANT; INHIBITION; DAMAGE; PROLIFERATION; ACTIVATION; MECHANISMS; STRATEGIES;
D O I
10.3390/antiox10081252
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
Resveratrol (RES) and oxyresveratrol (OXYRES) are considered and utilized as active ingredients of anti-aging skin cosmetics. However, these compounds are susceptible to oxidative discoloration and unpleasant odor in solutions, limiting their use in cosmetics. Accordingly, RES and OXYRES were chemically modified to acetylated derivatives with enhanced stability, and their anti-aging effect on the skin and detailed molecular mechanism of their acetylated derivatives were investigated. Acetylated RES and OXYRES lost their acetyl group and exerted an inhibitory effect on H2O2-induced ROS levels in human dermal fibroblast (HDF) cells. In addition, RES, OXYRES, and their acetylated derivatives suppressed UVB-induced matrix metalloproteinase (MMP)-1 expression via inhibition of mitogen-activated protein kinases (MAPKs) and Akt/mTOR signaling pathways. Furthermore, RES, OXYRES, and their acetylated derivatives suppressed type I collagen in TPA-treated HDF cells. Collectively, these results suggest the beneficial effects and underlying molecular mechanisms of RES, OXYRES, and their acetylated derivatives for anti- skin aging applications.
引用
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页数:18
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