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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/14661
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dc.contributor.authorAtli, Mehmet O.-
dc.contributor.authorBender, Robb W.-
dc.contributor.authorMehta, Vatsal-
dc.contributor.authorBastos, Michele R.-
dc.contributor.authorLuo, Wenxiang-
dc.contributor.authorVezina, Chad M.-
dc.contributor.authorWiltbank, Milo C.-
dc.date.accessioned2013-09-30T18:28:53Z-
dc.date.accessioned2014-05-20T13:42:10Z-
dc.date.accessioned2016-10-25T16:57:04Z-
dc.date.available2013-09-30T18:28:53Z-
dc.date.available2014-05-20T13:42:10Z-
dc.date.available2016-10-25T16:57:04Z-
dc.date.issued2012-04-01-
dc.identifierhttp://dx.doi.org/10.1095/biolreprod.111.094870-
dc.identifier.citationBiology of Reproduction. Madison: Soc Study Reproduction, v. 86, n. 4, p. 13, 2012.-
dc.identifier.issn0006-3363-
dc.identifier.urihttp://hdl.handle.net/11449/14661-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/14661-
dc.description.abstractNatural luteolysis involves multiple pulses of prostaglandin F2alpha (PGF) released by the nonpregnant uterus. This study investigated expression of 18 genes from five distinct pathways, following multiple low-dose pulses of PGF. Cows on Day 9 of the estrous cycle received four intrauterine infusions of 0.25 ml of phosphate-buffered saline (PBS) or PGF (0.5 mg of PGF in 0.25 ml of PBS) at 6-h intervals. A luteal biopsy sample was collected 30 min after each PBS or PGF infusion. There were four treatment groups: Control (n = 5; 4 PBS infusions), 4XPGF (4 PGF infusions; n = 5), 2XPGF-non-regressed (2 PGF infusions; n = 5; PGF-PBS-PGF-PBS; no regression after treatments), and 2XPGF-regressed (PGF-PBS-PGF-PBS; regression after treatments; n = 5). As expected, the first PGF pulse increased mRNA for the immediate early genes JUN, FOS, NR4A1, and EGR1 but unexpectedly also increased mRNA for steroidogenic (STAR) and angiogenic (VEGFA) pathways. The second PGF pulse induced immediate early genes and genes related to immune system activation (IL1B, FAS, FASLG, IL8). However, mRNA for VEGFA and STAR were decreased by the second PGF infusion. After the third and fourth PGF pulses, a distinctly luteolytic pattern of gene expression was evident, with inhibition of steroidogenic and angiogenic pathways, whereas, there was induction of pathways for immune system activation and production of PGF. The pattern of PGF-induced gene expression was similar in corpus luteum not destined for luteolysis (2X-non-regressed) after the first PGF pulse but was very distinct after the second PGF pulse. Thus, although the initial PGF pulse induced mRNA for many pathways, the second and later pulses of PGF appear to have set the distinct pattern of gene expression that result in luteolysis.en
dc.description.sponsorshipNational Institutes of Health-
dc.description.sponsorshipWisconsin Experiment Station-
dc.description.sponsorshipCouncil of Higher Education, Turkey-
dc.format.extent13-
dc.language.isoeng-
dc.publisherSoc Study Reproduction-
dc.sourceWeb of Science-
dc.subjectcorpus luteumen
dc.subjectgene expressionen
dc.subjecthormone actionen
dc.subjectluteolysisen
dc.subjectmRNAen
dc.subjectprostaglandinsen
dc.titlePatterns of Gene Expression in the Bovine Corpus Luteum Following Repeated Intrauterine Infusions of Low Doses of Prostaglandin F2alphaen
dc.typeoutro-
dc.contributor.institutionUniv Wisconsin-
dc.contributor.institutionDicle Univ-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv Wisconsin, Endocrinol Reprod Physiol Program, Madison, WI 53706 USA-
dc.description.affiliationUniv Wisconsin, Dept Dairy Sci, Madison, WI 53706 USA-
dc.description.affiliationDicle Univ, Dept ObGyn, Fac Vet Med, Diyarbakir, Turkey-
dc.description.affiliationUniv Wisconsin, Sch Vet Med, Dept Comparat Biosci, Madison, WI 53706 USA-
dc.description.affiliationSão Paulo State Univ, Dept Anim Reprod & Vet Radiol, São Paulo, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Dept Anim Reprod & Vet Radiol, São Paulo, Brazil-
dc.description.sponsorshipIdNIH: R01-HD050616-
dc.identifier.doi10.1095/biolreprod.111.094870-
dc.identifier.wosWOS:000306549500018-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofBiology of Reproduction-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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