{"title":"Inhibitory effect of tannic acid on iron–dextran-augmented and 7,12-dimethyl benz(a)anthracene-initiated skin carcinogenesis","authors":"Hossein Babaei, Ali Reza Mohajjel Nayebi, Hassan Rezazadeh, Mohamed Abdulla","doi":"10.1002/jtra.10049","DOIUrl":null,"url":null,"abstract":"Tannic acid (TA) is naturally occurring polyphenol present in fruits and vegetables. In this study we report that TA inhibits the carcinogenic effect of 7,12-dimethylbenz(a)anthracene (DMBA) in normal and iron-overloaded mice skin. Albino Swiss mice were given iron–dextran and pretreated with a single topical application of tannic acid; after 1 h, tumors were initiated by multiple topically application of DMBA. Appearance, number, and percent tumor incidence were recorded. When compared with the control group, the pretreated groups showed a significantly higher inhibition of tumor incidence. The induction of [3H]thymidine incorporation in cutaneous DNA and lipid peroxidation was inhibited in TA-pertreated animals as compared with the normal control group. Based on this study, we propose that TA significantly inhibits the augmentation potential of iron–dextran. A depletion in lipid peroxidation levels in TA-pretreated groups indicates that excessive generated oxidants in the mice skin tissues may be quenched by TA and because of the chelation of redox active iron and its faster elimination from the body. In conclusion, our data suggest that TA may be an effective chemopreventive agent and may offer protection against iron mediated skin cancer. J. Trace Elem. Exp. Med. 17:21–29, 2004. © 2004 Wiley-Liss, Inc.","PeriodicalId":101243,"journal":{"name":"The Journal of Trace Elements in Experimental Medicine","volume":"17 1","pages":"21-29"},"PeriodicalIF":0.0000,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jtra.10049","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Trace Elements in Experimental Medicine","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jtra.10049","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
单宁酸对铁-葡聚糖增强和7,12-二甲基苯(a)蒽引发的皮肤癌变的抑制作用
单宁酸(TA)是存在于水果和蔬菜中的天然多酚。在本研究中,我们报道了TA抑制7,12-二甲基苯(a)蒽(DMBA)在正常和铁过载小鼠皮肤中的致癌作用。给予Albino Swiss小鼠铁-葡聚糖,并用单次局部应用单宁酸进行预处理;1小时后,通过多次局部应用DMBA引发肿瘤。记录肿瘤的外观、数量和发病率。与对照组相比,预处理组对肿瘤发生率的抑制作用显著更高。与正常对照组相比,TA处理动物的[3H]胸苷掺入皮肤DNA和脂质过氧化的诱导受到抑制。基于这项研究,我们提出TA显著抑制铁-葡聚糖的增强潜力。TA预处理组脂质过氧化水平的降低表明,由于氧化还原活性铁的螯合作用及其更快地从体内清除,小鼠皮肤组织中过量产生的氧化剂可能被TA猝灭。总之,我们的数据表明TA可能是一种有效的化学预防剂,并可能对铁介导的皮肤癌症提供保护。J.Trace Elem。Exp.Med.17:21-292004。©2004 Wiley-Liss,股份有限公司。
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