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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/14620
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dc.contributor.authorMonteiro, G. A.-
dc.contributor.authorPapa, Frederico Ozanam-
dc.contributor.authorZahn, F. S.-
dc.contributor.authorDell'aqua Junior, José Antônio-
dc.contributor.authorMelo, C. M.-
dc.contributor.authorMaziero, R. R. D.-
dc.contributor.authorAvanzi, B. R.-
dc.contributor.authorAlvarenga, Marco Antonio-
dc.contributor.authorGuasti, P. N.-
dc.date.accessioned2013-09-30T18:28:40Z-
dc.date.accessioned2014-05-20T13:42:05Z-
dc.date.accessioned2016-10-25T16:56:59Z-
dc.date.available2013-09-30T18:28:40Z-
dc.date.available2014-05-20T13:42:05Z-
dc.date.available2016-10-25T16:56:59Z-
dc.date.issued2011-09-01-
dc.identifierhttp://dx.doi.org/10.1016/j.anireprosci.2011.08.002-
dc.identifier.citationAnimal Reproduction Science. Amsterdam: Elsevier B.V., v. 127, n. 3-4, p. 197-201, 2011.-
dc.identifier.issn0378-4320-
dc.identifier.urihttp://hdl.handle.net/11449/14620-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/14620-
dc.description.abstractThe cryopreservation of epididymal sperm is important to preserve genetic material from valuable deceased males. This study evaluated the viability of sperm samples from eight stallions under three conditions: (1) collected using an artificial vagina (EJ-0 h), (2) recovered from the epididymal cauda immediately after orchiectomy (EP-0 h), and (3) recovered from the epididymal cauda after 24 h of storage at 5 degrees C (EP-24 h). To obtain EJ-0 h sperm, two ejaculates were collected from each stallion. After 1 week, the stallions were submitted to bilateral orchiectomy, and one of the removed epididymides was flushed to obtain EP-0 h sperm. The contralateral epididymis was stored at 5 degrees C for 24 h before being flushed to obtain EP-24 h sperm. The sperm samples were analyzed at three different times: immediately after sperm recovery, after dilution in the freezing extender, and post-thawing. A fertility trial was performed using 39 estrous cycles. After ovulation induction with 1 mg of deslorelin acetate (i.m.), mares were inseminated with 800 x 10(6) sperm. The total number of sperm recovered was 7.8 +/- 4.7 x 10(9) for EJ-0 h sperm, 12.9 +/- 9.2 x 10(9) for EP-0 h sperm and 12.0 +/- 8.0 x 10(9) for EP-24 h sperm. The sperm motility, evaluated by total motility, progressive motility and the percentage of rapid cells, was similar among the samples before and after freezing (P > 0.05). However, the plasma membrane integrity was different between EJ-0 h and EP-0 h pre-freezing and between EJ-0 h and EP-24 h post-thawing (P < 0.05). The conception rates were similar between groups inseminated with sperm recovered from the epididymal cauda immediately after orchiectomy (EP-0 h), after 24 h of storage at 5 degrees C of the epididymal cauda (EP-24 h) and with ejaculated sperm (EJ-0 h) (P > 0.05). In conclusion, the viability and fertility of cauda epididymal sperm are similar to those of ejaculated sperm. (C) 2011 Elsevier B.V. All rights reserved.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.format.extent197-201-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectPregnancy rateen
dc.subjectEpididymal spermatozoaen
dc.subjectStallionen
dc.subjectCryopreservationen
dc.subjectSperm viabilityen
dc.titleCryopreservation and fertility of ejaculated and epididymal stallion spermen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUNESP, Sch Vet Med & Anim Sci, Dept Anim Reprod & Vet Radiol, BR-18610970 Botucatu, SP, Brazil-
dc.description.affiliationUnespUNESP, Sch Vet Med & Anim Sci, Dept Anim Reprod & Vet Radiol, BR-18610970 Botucatu, SP, Brazil-
dc.identifier.doi10.1016/j.anireprosci.2011.08.002-
dc.identifier.wosWOS:000296531300012-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofAnimal Reproduction Science-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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