dc.creator | Salazar, Inés | |
dc.creator | Tarragó-Litvak, Laura | |
dc.creator | Litvak, Simón | |
dc.creator | Gil, Lionel | |
dc.date.accessioned | 2019-01-29T14:47:11Z | |
dc.date.available | 2019-01-29T14:47:11Z | |
dc.date.created | 2019-01-29T14:47:11Z | |
dc.date.issued | 1985 | |
dc.identifier | Biochemical Pharmacology, Volumen 34, Issue 6, 2018, Pages 755-762 | |
dc.identifier | 00062952 | |
dc.identifier | 10.1016/0006-2952(85)90754-3 | |
dc.identifier | https://repositorio.uchile.cl/handle/2250/160569 | |
dc.description.abstract | When 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.language | en | |
dc.rights | http://creativecommons.org/licenses/by-nc-nd/3.0/cl/ | |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Chile | |
dc.source | Biochemical Pharmacology | |
dc.subject | Biochemistry | |
dc.subject | Pharmacology | |
dc.title | Effect of benzo[a]pyrene on DNA synthesis and DNA polymerase activity of rat liver nuclei | |
dc.type | Artículo de revista | |