Inhibition of UVB-mediated oxidative stress and markers of photoaging in immortalized HaCaT keratinocytes by pomegranate polyphenol extract POMx

被引:96
作者
Abu Zaid, Mohammad
Afaq, Farrukh
Syed, Deeba N.
Dreher, Mark
Mukhtar, Hasan [1 ]
机构
[1] Univ Wisconsin, Dept Dermatol, Madison, WI USA
[2] POM Wonderful Inc, Los Angeles, CA USA
关键词
D O I
10.1111/j.1751-1097.2007.00157.x
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
In recent years there has been an increase in use of botanicals with antioxidant properties as skin photoprotective agents. Pomegranate (Punica granatum L.) fruit possesses strong antioxidant and antiinflammatory properties. Recently, we have shown that pomegranate-derived products rich in anthocyanidins; and ellagitannins inhibit UVB-mediated activation of nuclear factor kappa B and modulate UVA-mediated cell proliferation pathways in normal human epidermal keratinocytes. In this study, we evaluated the effect of polyphenol-rich pomegranate fruit extract (POMx) on UVB-induced oxidative stress and photoaging in human immortalized HaCaT keratinocytes. Our data show that pretreatment of HaCaT cells with POMx (10-40 mu g mL(-1)) inhibited UVB (15-30 mJ cm(-2))-mediated (1) decrease in cell viability, (2) decrease in intracellular glutathione content and (3) increase in lipid peroxidation. Employing immunoblot analysis we found that pretreatment of HaCaT cells with POMx inhibited UVB-induced (1) upregulation of MMP-1, -2, -7 and -9, (2) decrease in TIMP-1, (3) phosphorylation of MAPKs and (iv) phosphorylation of c-jun, whereas no effect was observed on UVB-induced c-fos protein levels. These results suggest that POMx protects HaCaT cells against UVB-induced oxidative stress and markers of photoaging and could be a useful supplement in skin care products.
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收藏
页码:882 / 888
页数:7
相关论文
共 45 条
[11]   Ultraviolet-B irradiation and matrix metalloproteinases - From induction via signaling to initial events [J].
Brenneisen, P ;
Sies, H ;
Scharffetter-Kochanek, K .
CELL SIGNALING, TRANSCRIPTION, AND TRANSLATION AS THERAPEUTIC TARGETS, 2002, 973 :31-43
[12]   Modulation of skin collagen metabolism in aged and photoaged human skin in vivo [J].
Chung, JH ;
Seo, JY ;
Choi, HR ;
Lee, MK ;
Youn, CS ;
Rhie, GE ;
Cho, KH ;
Kim, KH ;
Park, KC ;
Eun, HC .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2001, 117 (05) :1218-1224
[13]  
DAVIS RJ, 1993, J BIOL CHEM, V268, P14553
[14]   Photochemoprevention of skin cancer by botanical agents [J].
F'guyer, S ;
Afaq, F ;
Mukhtar, H .
PHOTODERMATOLOGY PHOTOIMMUNOLOGY & PHOTOMEDICINE, 2003, 19 (02) :56-72
[15]  
Fisher GJ, 2005, CUTIS, V75, P5
[16]   Retinoic acid inhibits induction of c-Jun protein by ultraviolet radiation that occurs subsequent to activation of mitogen-activated protein kinase pathways in human skin in vivo [J].
Fisher, GJ ;
Talwar, HS ;
Lin, JY ;
Lin, PP ;
McPhillips, F ;
Wang, ZQ ;
Li, XY ;
Wan, YS ;
Kang, SW ;
Voorhees, JJ .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (06) :1432-1440
[17]   Mechanisms of photoaging and chronological skin aging [J].
Fisher, GJ ;
Kang, SW ;
Varani, J ;
Bata-Csorgo, Z ;
Wan, YS ;
Datta, S ;
Voorhees, JJ .
ARCHIVES OF DERMATOLOGY, 2002, 138 (11) :1462-1470
[18]   AGING AND PHOTOAGING OF THE SKIN - OBSERVATIONS AT THE CELLULAR AND MOLECULAR-LEVEL [J].
GILCHREST, BA ;
YAAR, M .
BRITISH JOURNAL OF DERMATOLOGY, 1992, 127 :25-30
[19]   Inflammation, gene mutation and photoimmunosuppression in response to UVR-induced oxidative damage contributes to photocarcinogenesis [J].
Halliday, GA .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2005, 571 (1-2) :107-120
[20]   Molecular mechanisms of skin ageing [J].
Jenkins, G .
MECHANISMS OF AGEING AND DEVELOPMENT, 2002, 123 (07) :801-810