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Ovine conceptus secretory proteins and bovine recombinant interferon alpha (1)-1 decrease endometrial oxytocin receptor concentrations in cyclic and progesterone-treated ovariectomized ewes.

作者信息

Vallet J L, Lamming G E

机构信息

AFRC Research Group on Hormones and Farm Animal Reproduction, University of Nottingham, Sutton Bonington, Loughborough.

出版信息

J Endocrinol. 1991 Dec;131(3):475-82. doi: 10.1677/joe.0.1310475.

DOI:10.1677/joe.0.1310475
PMID:1664451
Abstract

A series of experiements was performed to determine whether proteins produced by the sheep conceptus (oCSP) during the time of maternal recognition of pregnancy or bovine recombinant interferon alpha 1-1 (brIFN) decrease oxytocin receptor concentrations in the endometrium of cyclic or ovariectomized progesterone-treated ewes. In experiment 1, cyclic ewes received intrauterine infusions of serum proteins (oSP), oCSP or brIFN on days 12, 13 and 14 of the oestrous cycle. Ewes then received an oxytocin challenge (1 microgram in 0.9% NaCl), and blood samples were taken just before and every 10 min for 1 h after the challenge; these were measured for 13,14-dihydro-15-ketoprostaglandin F 2 alpha (PGFM), the stable metabolite of prostaglandin F 2 alpha. Endometrial oxytocin receptor concentrations were then measured. The oCSP and brIFN treatments suppressed both endometrial oxytocin receptor concentrations and oxytocin-induced increases in PGFM concentrations. In experiment 2, ewes were ovariectomized and then pretreated with a fluorogestone acetate-releasing intravaginal device for 10 days followed by oestradiol (25 micrograms i.m. twice daily for 2 days). Ewes were then treated with progesterone (10 mg i.m. twice daily for 12 days). Ewes received intrauterine infusions of oSP, oCSP and brIFN on days 10, 11 and 12 of progesterone treatment. On the day after the last progesterone treatment, ewes were challenged with oxytocin and blood samples collected to measure PGFM. Endometrial oxytocin receptors were also measured. Treatment with oCSP, but not brIFN, suppressed endometrial concentrations of oxytocin receptor, and neither oCSP nor brIFN altered oxytocin-induced increases in PGFM concentrations.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

相似文献

1
Ovine conceptus secretory proteins and bovine recombinant interferon alpha (1)-1 decrease endometrial oxytocin receptor concentrations in cyclic and progesterone-treated ovariectomized ewes.
J Endocrinol. 1991 Dec;131(3):475-82. doi: 10.1677/joe.0.1310475.
2
Effects of ovine conceptus secretory proteins and progesterone on oxytocin-stimulated endometrial production of prostaglandin and turnover of inositol phosphate in ovariectomized ewes.绵羊孕体分泌蛋白和孕酮对去卵巢母羊中催产素刺激的子宫内膜前列腺素生成及肌醇磷酸代谢的影响。
J Reprod Fertil. 1992 May;95(1):19-29. doi: 10.1530/jrf.0.0950019.
3
Effect of ovine conceptus secretory proteins and purified ovine trophoblast protein-1 on interoestrous interval and plasma concentrations of prostaglandins F-2 alpha and E and of 13,14-dihydro-15-keto prostaglandin F-2 alpha in cyclic ewes.绵羊孕体分泌蛋白和纯化的绵羊滋养层蛋白-1对周期性发情母羊发情间期以及前列腺素F-2α、E和13,14-二氢-15-酮前列腺素F-2α血浆浓度的影响。
J Reprod Fertil. 1988 Nov;84(2):493-504. doi: 10.1530/jrf.0.0840493.
4
Ovine trophoblast protein-one inhibits development of endometrial responsiveness to oxytocin in ewes.
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Administration of recombinant bovine interferon-alpha I at the time of maternal recognition of pregnancy inhibits prostaglandin F2 alpha secretion and causes luteal maintenance in cyclic ewes.在母羊识别妊娠时给予重组牛α-干扰素I可抑制前列腺素F2α的分泌,并使周期发情母羊的黄体得以维持。
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6
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Changes in progesterone and oestrogen receptor mRNA and protein and oxytocin receptors in endometrium of ewes after intrauterine injection of ovine trophoblast interferon.
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Intrauterine injection of ovine interferon-tau alters oestrogen receptor and oxytocin receptor expression in the endometrium of cyclic ewes.子宫内注射绵羊干扰素-tau会改变周期性母羊子宫内膜中雌激素受体和催产素受体的表达。
J Mol Endocrinol. 1995 Oct;15(2):203-20. doi: 10.1677/jme.0.0150203.
10
Increases in the oxytocin-induced prostaglandin F2 alpha response and reduction in the concentrations of endometrial oxytocin receptors in ewes in response to progesterone.
J Reprod Fertil. 1992 May;95(1):11-8. doi: 10.1530/jrf.0.0950011.

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