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石榴衍生产品对紫外线B介导的人重组皮肤损伤的保护作用。

Protective effect of pomegranate-derived products on UVB-mediated damage in human reconstituted skin.

作者信息

Afaq Farrukh, Zaid Mohammad Abu, Khan Naghma, Dreher Mark, Mukhtar Hasan

机构信息

Department of Dermatology, University of Wisconsin, Madison, WI 53706, USA.

出版信息

Exp Dermatol. 2009 Jun;18(6):553-61. doi: 10.1111/j.1600-0625.2008.00829.x. Epub 2009 Mar 6.

Abstract

Solar ultraviolet (UV) radiation, particularly its UVB (290-320 nm) component, is the primary cause of many adverse biological effects including photoageing and skin cancer. UVB radiation causes DNA damage, protein oxidation and induces matrix metalloproteinases (MMPs). Photochemoprevention via the use of botanical antioxidants in affording protection to human skin against UVB damage is receiving increasing attention. Pomegranate, from the tree Punica granatum, contains anthocyanins and hydrolysable tannins and possesses strong antioxidant and anti-tumor-promoting properties. In this study, we determined the effect of pomegranate-derived products--POMx juice, POMx extract and pomegranate oil (POMo)--against UVB-mediated damage using reconstituted human skin (EpiDerm(TM) FT-200). EpiDerm was treated with POMx juice (1-2 microl/0.1 ml/well), POMx extract (5-10 microg/0.1 ml/well) and POMo (1-2 microl/0.1 ml/well) for 1 h prior to UVB (60 mJ/cm(2)) irradiation and was harvested 12 h post-UVB to assess protein oxidation, markers of DNA damage and photoageing by Western blot analysis and immunohistochemistry. Pretreatment of Epiderm with pomegranate-derived products resulted in inhibition of UVB-induced (i) cyclobutane pyrimidine dimers (CPD), (ii) 8-dihydro-2'-deoxyguanosine (8-OHdG), (iii) protein oxidation and (iv) proliferating cell nuclear antigen (PCNA) protein expression. We also found that pretreatment of Epiderm with pomegranate-derived products resulted in inhibition of UVB-induced (i) collagenase (MMP-1), (ii) gelatinase (MMP-2, MMP-9), (iii) stromelysin (MMP-3), (iv) marilysin (MMP-7), (v) elastase (MMP-12) and (vi) tropoelastin. Gelatin zymography revealed that pomegranate-derived products inhibited UVB-induced MMP-2 and MMP-9 activities. Pomegranate-derived products also caused a decrease in UVB-induced protein expression of c-Fos and phosphorylation of c-Jun. Collectively, these results suggest that all three pomegranate-derived products may be useful against UVB-induced damage to human skin.

摘要

太阳紫外线(UV)辐射,尤其是其中的UVB(290 - 320纳米)成分,是许多不良生物学效应的主要原因,包括光老化和皮肤癌。UVB辐射会导致DNA损伤、蛋白质氧化并诱导基质金属蛋白酶(MMPs)。通过使用植物抗氧化剂进行光化学预防,以保护人类皮肤免受UVB损伤,正受到越来越多的关注。石榴树(Punica granatum)所产的石榴含有花青素和可水解单宁,并具有强大的抗氧化和抗肿瘤促进特性。在本研究中,我们使用重组人皮肤(EpiDerm™ FT - 200),测定了石榴衍生产品——POMx果汁、POMx提取物和石榴油(POMo)——对UVB介导损伤的影响。在UVB(60 mJ/cm²)照射前1小时,用POMx果汁(1 - 2微升/0.1毫升/孔)、POMx提取物(5 - 10微克/0.1毫升/孔)和POMo(1 - 2微升/0.1毫升/孔)处理EpiDerm,并在UVB照射后12小时收获,通过蛋白质印迹分析和免疫组织化学评估蛋白质氧化、DNA损伤标志物和光老化情况。用石榴衍生产品预处理EpiDerm可导致对UVB诱导的(i)环丁烷嘧啶二聚体(CPD)、(ii)8 - 二氢 - 2'-脱氧鸟苷(8 - OHdG)、(iii)蛋白质氧化和(iv)增殖细胞核抗原(PCNA)蛋白表达的抑制。我们还发现,用石榴衍生产品预处理EpiDerm可导致对UVB诱导的(i)胶原酶(MMP - 1)、(ii)明胶酶(MMP - 2、MMP - 9)、(iii)基质溶解素(MMP - 3)、(iv)膜型基质金属蛋白酶 - 7(MMP - 7)、(v)弹性蛋白酶(MMP - 12)和(vi)原弹性蛋白的抑制。明胶酶谱分析显示,石榴衍生产品可抑制UVB诱导的MMP - 2和MMP - 9活性。石榴衍生产品还导致UVB诱导的c - Fos蛋白表达和c - Jun磷酸化的降低。总体而言,这些结果表明,所有三种石榴衍生产品可能对UVB诱导的人类皮肤损伤有用。

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