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[PMID]: | 27773348 |
[Au] Autor: | Rebordão MR; Galvão A; Pinto-Bravo P; Pinheiro J; Gamboa S; Silva E; Mateus L; Ferreira-Dias G |
[Ad] Endereço: | CIISA, Faculty of Veterinary Medicine, University of Lisbon, Lisbon, Portugal; Department of Animal Science, Coimbra College of Agriculture, Coimbra, Portugal. |
[Ti] Título: | Endometrial prostaglandin synthases, ovarian steroids, and oxytocin receptors in mares with oxytocin-induced luteal maintenance. |
[So] Source: | Theriogenology;87:193-204, 2017 Jan 01. | [Is] ISSN: | 1879-3231 |
[Cp] País de publicação: | United States |
[La] Idioma: | eng |
[Ab] Resumo: | Oxytocin (OXT) has been used to prolong the luteal phase in mares, but its mechanism of action is unknown. The aim of this study was to evaluate the effect of chronic exogenous OXT administration to mid-luteal phase mares on luteal maintenance. Also, endometrial expression of prostaglandin endoperoxide synthase 2 (PTGS2), prostaglandin F α, E and I synthases (AKR1C3, PTGES, and PTGIS), oxytocin receptor (OXTR), progesterone receptor (PGR), and estrogen receptors 1 (ESR1) and 2 (ESR2) were assessed in mares experiencing luteal maintenance 2 weeks after chronic exogenous OXT administration. Control mares (n = 5; C group) received 6 mL of saline im, whereas OXT (60 units/mare) was administered im (n = 6; OXT group), every 12 hours, on days 7 to 14 postovulation. After endometrial biopsy in groups C (Day 10) and OXT (Day 24), luteolysis occurred within 3 or 6 days, respectively. Luteal maintenance took place in 4 of 6 (67%) of OXT-treated mares. Progesterone in C group was the highest on biopsy day (P < 0.05). In OXT mares, PTGS2, ESR1 (P < 0.05), PTGES, PTGIS, PGR, and ESR2 (P < 0.01) gene transcription decreased, whereas OXTR increased (P < 0.05) in comparison with the C group. In OXT-treated mares, endometrial ESR2 protein expression decreased (P < 0.05), but OXTR increased (P < 0.05) compared with control animals. In both experimental groups, PTGS2 was mainly immunolocalized in surface epithelium, whereas AKR1C3, PTGES, PTGIS, and PGR were in surface and glandular epithelia. ESR1 and ESR2 were found in glandular epithelium and OXTR in stromal cells. High immunolabeling for PTGES, PTGIS, PGR, and OXTR and low for ESR2 was detected in endometrium of OXT-group mares with extended diestrus. Prolonged luteal function associated with chronic OXT treatment may be related to different spatial expression of OXTR and PGR in the endometrium. The observed reduction of endometrial ESR2 may be responsible for the maintenance of PGR in luminal and glandular epithelium. Also, ESR2 may attenuate the transcriptional activity of ESR1 in mare endometrium. This study offers new knowledge on the endometrial expression of ovarian steroids and OXT receptors in OXT pharmacologically induced luteal maintenance in the mare. |
[Mh] Termos MeSH primário: |
Corpo Lúteo/efeitos dos fármacos Cavalos/fisiologia Ovário/fisiologia Ocitocina/farmacologia Prostaglandina-Endoperóxido Sintases/metabolismo Receptores de Ocitocina/metabolismo
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[Mh] Termos MeSH secundário: |
Animais Corpo Lúteo/fisiologia Estrogênios/genética Estrogênios/metabolismo Feminino Ocitócicos/farmacologia Progestinas/genética Progestinas/metabolismo Prostaglandina-Endoperóxido Sintases/genética Receptores Estrogênicos/genética Receptores Estrogênicos/metabolismo Receptores de Ocitocina/genética Receptores de Progesterona/genética Receptores de Progesterona/metabolismo
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[Pt] Tipo de publicação: | JOURNAL ARTICLE |
[Nm] Nome de substância:
| 0 (Estrogens); 0 (Oxytocics); 0 (Progestins); 0 (Receptors, Estrogen); 0 (Receptors, Oxytocin); 0 (Receptors, Progesterone); 50-56-6 (Oxytocin); EC 1.14.99.1 (Prostaglandin-Endoperoxide Synthases) |
[Em] Mês de entrada: | 1704 |
[Cu] Atualização por classe: | 171201 |
[Lr] Data última revisão:
| 171201 |
[Sb] Subgrupo de revista: | IM |
[Da] Data de entrada para processamento: | 161025 |
[St] Status: | MEDLINE |
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