Institute of Human Nutrition and Food Science, Christian-Albrechts-University Kiel, Hermann-Rodewald-Strasse 6, Kiel, Germany.
Br J Nutr. 2012 Feb;107(3):360-3. doi: 10.1017/S0007114511002984. Epub 2011 Jul 12.
There is increasing interest in the gene-regulatory activities of isothiocyanates and flavonoids in human skin. Nrf2 agonists, such as isothiocyanate sulforaphane (SFN), have been shown to promote chemopreventive effects in skin both in vitro and in vivo. Recent data indicate that different secondary plant compounds may either antagonise or enhance SFN-induced Nrf2 activation. We therefore studied the interactions of a flavonoid, cyanidin and the potent Nrf2 inductor SFN in cultured human keratinocytes (HaCaT cells). We observed that cyanidin does not induce the activation of Nrf2 and its target genes, γ-glutamylcysteine synthetase (γGCS), NAD(P)H:quinone oxidoreductase 1 and haem oxygenase-1 in HaCaT cells. Furthermore, SFN-mediated Nrf2 activation and its target gene expression were not further enhanced by the co-application of SFN with cyanidin.
人们对异硫氰酸酯和类黄酮在人类皮肤中的基因调控活性越来越感兴趣。已经表明,Nrf2 激动剂,如异硫氰酸酯萝卜硫素(SFN),在体外和体内都能促进皮肤的化学预防作用。最近的数据表明,不同的次生植物化合物可能拮抗或增强 SFN 诱导的 Nrf2 激活。因此,我们研究了类黄酮花青素和强效 Nrf2 诱导剂 SFN 在培养的人角质形成细胞(HaCaT 细胞)中的相互作用。我们观察到花青素本身不会诱导 Nrf2 及其靶基因γ-谷氨酰半胱氨酸合成酶(γGCS)、NAD(P)H:醌氧化还原酶 1 和血红素加氧酶-1 在 HaCaT 细胞中的激活。此外,SFN 介导的 Nrf2 激活及其靶基因表达也不会因 SFN 与花青素的共同应用而进一步增强。