dc.creatorSalazar, Inés
dc.creatorTarragó-Litvak, Laura
dc.creatorLitvak, Simón
dc.creatorGil, Lionel
dc.date.accessioned2019-01-29T14:47:11Z
dc.date.available2019-01-29T14:47:11Z
dc.date.created2019-01-29T14:47:11Z
dc.date.issued1985
dc.identifierBiochemical Pharmacology, Volumen 34, Issue 6, 2018, Pages 755-762
dc.identifier00062952
dc.identifier10.1016/0006-2952(85)90754-3
dc.identifierhttps://repositorio.uchile.cl/handle/2250/160569
dc.description.abstractWhen benzo[a]pyrene (B[a]P) was administered intraperitoneally to rats 48 hr before they were killed, the DNA-synthesizing capability of isolated rat liver nuclei was decreased as compared with control animals. B[a]P also inhibited in vitro DNA synthesis in nuclei purified from control animals; this effect was enhanced by NADPH. DNA polymerases solubilized from purified nuclei of B[a]P-treated animals were less active than those of control animals. DNA polymerase α was more inhibited than DNA polymerase β. Purified rat liver nuclei devoid of cytoplasmic contamination possess an NADPH-dependent B[a]P hydroxylase activity. The observed inhibition of DNA synthesis in nuclei isolated from B[a]P-treated rats was increased by NADPH. Moreover, there was an increased inhibition of DNA polymerase activity by nuclear membranes obtained from B[a]P-treated animals when the incubations were performed in the presence of NADPH. Also, the derivative B[a]P-trans-9,10-dihydrodiol was a potent inhibitor
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceBiochemical Pharmacology
dc.subjectBiochemistry
dc.subjectPharmacology
dc.titleEffect of benzo[a]pyrene on DNA synthesis and DNA polymerase activity of rat liver nuclei
dc.typeArtículo de revista


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