dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorUniversidade Estadual de Campinas (UNICAMP)
dc.date.accessioned2015-10-21T13:10:52Z
dc.date.available2015-10-21T13:10:52Z
dc.date.created2015-10-21T13:10:52Z
dc.date.issued2015-06-01
dc.identifierReproductive Toxicology. Oxford: Pergamon-elsevier Science Ltd, v. 53, p. 1-9, 2015.
dc.identifier0890-6238
dc.identifierhttp://hdl.handle.net/11449/128548
dc.identifier10.1016/j.reprotox.2015.02.010
dc.identifierWOS:000356318900001
dc.identifier7263490918934874
dc.identifier1739564105219382
dc.identifier5760560970751598
dc.identifier0000-0003-1452-5708
dc.description.abstractAll-trans retinoic acid (atRA) maintains physiological stability of the prostate, and we reported that ethanol intake increases atRA in the rat prostate; however the mechanisms underlying these changes are unknown. We evaluated the impact of a low- and high-dose ethanol intake (UChA and UChB strains) on atRA metabolism in the dorsal and lateral prostate. Aldehyde dehydrogenase (ALDH) subtype 1A3 was increased in the dorsal prostate of UChA animals while ALDH1A1 and ALDH1A2 decreased in the lateral prostate. In UChB animals, ALDH1A1, ALDH1A2, and ALDH1A3 increased in the dorsal prostate, and ALDH1A3 decreased in the lateral prostate. atRA levels increased with the low activity of CYP2E1 and decreased with high CYP26 activity in the UChB dorsal prostate. Conversely, atRA was found to decrease when the activity of total CYP was increased in the UChA lateral prostate. Ethanol modulates the synthesis and catabolism of atRA in the prostate in a concentration-dependent manner. (C) 2015 Elsevier Inc. All rights reserved.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationReproductive Toxicology
dc.relation2.580
dc.relation0,846
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectEthanol
dc.subjectAll-trans retinoic acid
dc.subjectALDH
dc.subjectCYP
dc.subjectProstate
dc.titleEthanol modulates the synthesis and catabolism of retinoic acid in the rat prostate
dc.typeArtículos de revistas


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