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dc.contributor.authorBabaei, H
dc.contributor.authorNayebi, ARM
dc.contributor.authorRezazadeh, H
dc.contributor.authorAbdulla, M
dc.date.accessioned2018-08-26T08:30:59Z
dc.date.available2018-08-26T08:30:59Z
dc.date.issued2004
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52077
dc.description.abstractTannic 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 I It, 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.
dc.language.isoEnglish
dc.relation.ispartofJOURNAL OF TRACE ELEMENTS IN EXPERIMENTAL MEDICINE
dc.subjecttannic acid
dc.subjectiron overload
dc.subject7,12-dimethylbenz(a)anthracene
dc.subjectskin cancer
dc.titleInhibitory effect of tannic acid on iron-dextran-augmented and 7,12-dimethylbenz(a)anthracene-initiated skin carcinogenesis
dc.typeArticle
dc.citation.volume17
dc.citation.issue1
dc.citation.spage21
dc.citation.epage29
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1002/jtra.10049


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