Hemodynamics of the corpus luteum in mares during experimentally impaired luteogenesis and partial luteolysis
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.theriogenology.2017.10.045 http://hdl.handle.net/11449/175460 |
Resumo: | The aim of the current project was to characterize the luteal vascularity and the plasma concentrations of progesterone (P4), prolactin (PRL) and 13,14-dihydro-15-keto-PGF2α (PGFM) in mares with luteal disturbances during early and mid-diestrus. In Experiment 1, twenty-one mares were treated with 2 mL of 0.9% NaCl, or 1 mg Dinoprost, or 10 mg Dinoprost on day two after ovulation (Control-D2, 1/10PGF-D2 and PGF-D2 groups, respectively; n = 7 mares/group). In Experiment 2, similar treatments were performed eight days post-ovulation using a different cohort of 21 mares (Control-D8, 1/10PGF-D8 and PGF-D8 groups, respectively; n = 7 mares/group). Blood samples were collected hourly and power-Doppler examinations of the corpus luteum (CL) were performed every 6 h from H0 (moment immediately before treatment) to H48. Data collection was also done once a day from D0 (day of ovulation) to D20. In Experiment 1, the PGF-D2 and 1/10PGF-D2 groups had lower increase of plasma concentration of P4 until H48 and reduced maximum P4 concentrations on D8-D11 than mares from the Control-D2 group. However, no differences among groups were detected for luteal vascularity during early and mid-diestrus. In Experiment 2, complete and partial luteolysis were detected in mares from the PGF-D8 and 1/10PGF-D8 groups, respectively. Luteal vascularity and plasma P4 concentrations differed among Control-D8, PGF-D8 and 1/10PGF-D8 groups on H48. Partially regressed CLs (1/10PGF-D8 group) generated more Doppler signals than completed regressed CLs (PGF-D8 group) between D10 and D13. In both experiments, a transient increase in PRL activity was observed in parallel to the PGFM pulse in mares receiving 1 or 10 mg Dinoprost. The use of prostaglandin on D2 at conventional or 1/10 of the dose impaired the luteal development in mares. Moreover, the low dose of prostaglandin lead to partial regression of mature CLs. The blood supply was reduced in partially regressed CLs, but not in CLs undergoing impaired luteogenesis. |
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Hemodynamics of the corpus luteum in mares during experimentally impaired luteogenesis and partial luteolysisDiestrusDoppler ultrasonographyPGFMProgesteroneProlactinThe aim of the current project was to characterize the luteal vascularity and the plasma concentrations of progesterone (P4), prolactin (PRL) and 13,14-dihydro-15-keto-PGF2α (PGFM) in mares with luteal disturbances during early and mid-diestrus. In Experiment 1, twenty-one mares were treated with 2 mL of 0.9% NaCl, or 1 mg Dinoprost, or 10 mg Dinoprost on day two after ovulation (Control-D2, 1/10PGF-D2 and PGF-D2 groups, respectively; n = 7 mares/group). In Experiment 2, similar treatments were performed eight days post-ovulation using a different cohort of 21 mares (Control-D8, 1/10PGF-D8 and PGF-D8 groups, respectively; n = 7 mares/group). Blood samples were collected hourly and power-Doppler examinations of the corpus luteum (CL) were performed every 6 h from H0 (moment immediately before treatment) to H48. Data collection was also done once a day from D0 (day of ovulation) to D20. In Experiment 1, the PGF-D2 and 1/10PGF-D2 groups had lower increase of plasma concentration of P4 until H48 and reduced maximum P4 concentrations on D8-D11 than mares from the Control-D2 group. However, no differences among groups were detected for luteal vascularity during early and mid-diestrus. In Experiment 2, complete and partial luteolysis were detected in mares from the PGF-D8 and 1/10PGF-D8 groups, respectively. Luteal vascularity and plasma P4 concentrations differed among Control-D8, PGF-D8 and 1/10PGF-D8 groups on H48. Partially regressed CLs (1/10PGF-D8 group) generated more Doppler signals than completed regressed CLs (PGF-D8 group) between D10 and D13. In both experiments, a transient increase in PRL activity was observed in parallel to the PGFM pulse in mares receiving 1 or 10 mg Dinoprost. The use of prostaglandin on D2 at conventional or 1/10 of the dose impaired the luteal development in mares. Moreover, the low dose of prostaglandin lead to partial regression of mature CLs. The blood supply was reduced in partially regressed CLs, but not in CLs undergoing impaired luteogenesis.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Department of Animal Reproduction and Veterinary Radiology School of Veterinary Medicine and Animal Science UNESPDepartment of Veterinary Clinical Medicine College of Veterinary Medicine University of IllinoisSchool of Animal Sciences Louisiana State University Agricultural CenterDepartment of Animal Reproduction and Veterinary Radiology School of Veterinary Medicine and Animal Science UNESPFAPESP: # 1070/2012FAPESP: 2012/122868-6Universidade Estadual Paulista (Unesp)University of IllinoisLouisiana State University Agricultural CenterFerreira, J. C. [UNESP]Filho, L.F. Novaes [UNESP]Boakari, Y. L. [UNESP]Canesin, H. S. [UNESP]Thompson, D. L.Lima, F. S.Meira, C. [UNESP]2018-12-11T17:15:55Z2018-12-11T17:15:55Z2018-02-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article78-84application/pdfhttp://dx.doi.org/10.1016/j.theriogenology.2017.10.045Theriogenology, v. 107, p. 78-84.0093-691Xhttp://hdl.handle.net/11449/17546010.1016/j.theriogenology.2017.10.0452-s2.0-850334057962-s2.0-85033405796.pdf00429054157111990000-0002-2245-800XScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengTheriogenologyinfo:eu-repo/semantics/openAccess2024-09-09T14:00:57Zoai:repositorio.unesp.br:11449/175460Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-09T14:00:57Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Hemodynamics of the corpus luteum in mares during experimentally impaired luteogenesis and partial luteolysis |
title |
Hemodynamics of the corpus luteum in mares during experimentally impaired luteogenesis and partial luteolysis |
spellingShingle |
Hemodynamics of the corpus luteum in mares during experimentally impaired luteogenesis and partial luteolysis Ferreira, J. C. [UNESP] Diestrus Doppler ultrasonography PGFM Progesterone Prolactin |
title_short |
Hemodynamics of the corpus luteum in mares during experimentally impaired luteogenesis and partial luteolysis |
title_full |
Hemodynamics of the corpus luteum in mares during experimentally impaired luteogenesis and partial luteolysis |
title_fullStr |
Hemodynamics of the corpus luteum in mares during experimentally impaired luteogenesis and partial luteolysis |
title_full_unstemmed |
Hemodynamics of the corpus luteum in mares during experimentally impaired luteogenesis and partial luteolysis |
title_sort |
Hemodynamics of the corpus luteum in mares during experimentally impaired luteogenesis and partial luteolysis |
author |
Ferreira, J. C. [UNESP] |
author_facet |
Ferreira, J. C. [UNESP] Filho, L.F. Novaes [UNESP] Boakari, Y. L. [UNESP] Canesin, H. S. [UNESP] Thompson, D. L. Lima, F. S. Meira, C. [UNESP] |
author_role |
author |
author2 |
Filho, L.F. Novaes [UNESP] Boakari, Y. L. [UNESP] Canesin, H. S. [UNESP] Thompson, D. L. Lima, F. S. Meira, C. [UNESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) University of Illinois Louisiana State University Agricultural Center |
dc.contributor.author.fl_str_mv |
Ferreira, J. C. [UNESP] Filho, L.F. Novaes [UNESP] Boakari, Y. L. [UNESP] Canesin, H. S. [UNESP] Thompson, D. L. Lima, F. S. Meira, C. [UNESP] |
dc.subject.por.fl_str_mv |
Diestrus Doppler ultrasonography PGFM Progesterone Prolactin |
topic |
Diestrus Doppler ultrasonography PGFM Progesterone Prolactin |
description |
The aim of the current project was to characterize the luteal vascularity and the plasma concentrations of progesterone (P4), prolactin (PRL) and 13,14-dihydro-15-keto-PGF2α (PGFM) in mares with luteal disturbances during early and mid-diestrus. In Experiment 1, twenty-one mares were treated with 2 mL of 0.9% NaCl, or 1 mg Dinoprost, or 10 mg Dinoprost on day two after ovulation (Control-D2, 1/10PGF-D2 and PGF-D2 groups, respectively; n = 7 mares/group). In Experiment 2, similar treatments were performed eight days post-ovulation using a different cohort of 21 mares (Control-D8, 1/10PGF-D8 and PGF-D8 groups, respectively; n = 7 mares/group). Blood samples were collected hourly and power-Doppler examinations of the corpus luteum (CL) were performed every 6 h from H0 (moment immediately before treatment) to H48. Data collection was also done once a day from D0 (day of ovulation) to D20. In Experiment 1, the PGF-D2 and 1/10PGF-D2 groups had lower increase of plasma concentration of P4 until H48 and reduced maximum P4 concentrations on D8-D11 than mares from the Control-D2 group. However, no differences among groups were detected for luteal vascularity during early and mid-diestrus. In Experiment 2, complete and partial luteolysis were detected in mares from the PGF-D8 and 1/10PGF-D8 groups, respectively. Luteal vascularity and plasma P4 concentrations differed among Control-D8, PGF-D8 and 1/10PGF-D8 groups on H48. Partially regressed CLs (1/10PGF-D8 group) generated more Doppler signals than completed regressed CLs (PGF-D8 group) between D10 and D13. In both experiments, a transient increase in PRL activity was observed in parallel to the PGFM pulse in mares receiving 1 or 10 mg Dinoprost. The use of prostaglandin on D2 at conventional or 1/10 of the dose impaired the luteal development in mares. Moreover, the low dose of prostaglandin lead to partial regression of mature CLs. The blood supply was reduced in partially regressed CLs, but not in CLs undergoing impaired luteogenesis. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-12-11T17:15:55Z 2018-12-11T17:15:55Z 2018-02-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.theriogenology.2017.10.045 Theriogenology, v. 107, p. 78-84. 0093-691X http://hdl.handle.net/11449/175460 10.1016/j.theriogenology.2017.10.045 2-s2.0-85033405796 2-s2.0-85033405796.pdf 0042905415711199 0000-0002-2245-800X |
url |
http://dx.doi.org/10.1016/j.theriogenology.2017.10.045 http://hdl.handle.net/11449/175460 |
identifier_str_mv |
Theriogenology, v. 107, p. 78-84. 0093-691X 10.1016/j.theriogenology.2017.10.045 2-s2.0-85033405796 2-s2.0-85033405796.pdf 0042905415711199 0000-0002-2245-800X |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Theriogenology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
78-84 application/pdf |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
_version_ |
1813546566358663168 |