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dc.contributor.authorWiltbank, M. C.
dc.contributor.authorMeidan, R.
dc.contributor.authorOchoa, J. [UNESP]
dc.contributor.authorBaez, G. M.
dc.contributor.authorGiordano, J. O.
dc.contributor.authorFerreira, J. C. P. [UNESP]
dc.contributor.authorSartori, R.
dc.date.accessioned2018-11-26T16:56:30Z
dc.date.available2018-11-26T16:56:30Z
dc.date.issued2016-07-01
dc.identifierhttp://dx.doi.org/10.21451/1984-3143-AR865
dc.identifier.citationAnimal Reproduction. Belo Horizonte: Brazilian Coll Animal Reproduction, v. 13, n. 3, p. 217-233, 2016.
dc.identifier.issn1806-9614
dc.identifier.urihttp://hdl.handle.net/11449/161859
dc.description.abstractIn ruminants, there are specific times during the estrous cycle or pregnancy when the corpus luteum (CL) may undergo regression. This review has attempted to summarize the physiological and cellular mechanisms involved in CL regression or maintenance during four distinct periods. The first period is near day 7 when animals that are ovulating after a period of low circulating progesterone (P4), such as first pubertal ovulation or first postpartum ovulation, are at risk of having a premature increase in Prostaglandin F2 alpha (PGF) secreted from the uterus resulting in early CL regression and a short estrous cycle. The second period is when normal luteolysis occurs at day 18-25 of the cycle or when the CL is rescued by interferon-tau secreted by the elongating embryo. The uterine mechanisms that determine the timing of this luteolysis or the prevention of luteolysis have been generally defined. Induction and activation of endometrial E2 receptors result in induction of endometrial oxytocin receptors that can now be activated by normal pulses of oxytocin. Of particular importance is the observation that the primary mechanisms are only activated through local (ipsilateral) and not a systemic route due to transfer of PGF from the uterine vein to the ovarian artery. In addition at the CL level, studies are providing definition to the cellular and molecular mechanisms that are activated in response to uterine PGF pulses or pregnancy. The third period that is discussed occurs in the second month of pregnancy (day 28-60) when undefined mechanisms result in CL maintenance of an ipsilateral CL but regression of a contralateral (opposite side from pregnancy) CL. The final period that is discussed is regression of the CL just prior to parturition. Although, cortisol from the fetus appears to be the primary initiator of luteolysis, PGF seems to be the final signal that causes regression of the CL. Thus, in all four periods, regression of the CL is likely to be caused by the direct actions of PGF that is secreted from the uterus. The uterine mechanisms that result in secretion of PGF seem to be normally inhibited during the early luteal phase, making short luteal phases not a normal event, and are altered during early pregnancy (day 18-25) resulting in prevention of luteolysis. During much of pregnancy, the mechanisms that cause PGF secretion from the uterus in response to oxytocin are intact but luteolysis does not normally occur, perhaps due to lack of efficient utero-ovarian transfer of PGF.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipBARD
dc.description.sponsorshipWisconsin Experiment Station
dc.format.extent217-233
dc.language.isoeng
dc.publisherBrazilian Coll Animal Reproduction
dc.relation.ispartofAnimal Reproduction
dc.sourceWeb of Science
dc.subjectinterferon-tau
dc.subjectluteolysis
dc.subjectprostaglandin F2 alpha
dc.titleMaintenance or regression of the corpus luteum during multiple decisive periods of bovine pregnancyen
dc.typeArtigo
dcterms.rightsHolderBrazilian Coll Animal Reproduction
dc.contributor.institutionUniv Wisconsin Madison
dc.contributor.institutionHebrew Univ Jerusalem
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionCornell Univ
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.description.affiliationUniv Wisconsin Madison, Dept Dairy Sci, Madison, WI 53706 USA
dc.description.affiliationHebrew Univ Jerusalem, Rehovot, Israel
dc.description.affiliationSao Paulo State Univ, Dept Anim Prod, Botucatu, SP, Brazil
dc.description.affiliationCornell Univ, Dept Anim Sci, Ithaca, NY 14853 USA
dc.description.affiliationUniv Sao Paulo, Dept Anim Sci, ESALQ, Piracicaba, SP, Brazil
dc.description.affiliationUnespSao Paulo State Univ, Dept Anim Prod, Botucatu, SP, Brazil
dc.identifier.doi10.21451/1984-3143-AR865
dc.identifier.wosWOS:000382285100010
dc.rights.accessRightsAcesso restrito
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