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前列腺素F2α作为猪的黄体溶解素:VI. 外源前列腺素F2α从子宫腔进入血管系统移动的激素调节。

Prostaglandin F2 alpha as the luteolysin in swine: VI. Hormonal regulation of the movement of exogenous PGF2 alpha from the uterine lumen into the vasculature.

作者信息

Marengo S R, Bazer F W, Thatcher W W, Wilcox C J, Wetteman R P

出版信息

Biol Reprod. 1986 Mar;34(2):284-92. doi: 10.1095/biolreprod34.2.284.

Abstract

To test the endocrine-exocrine theory of maternal recognition of pregnancy in the pig 16 gilts were assigned randomly to a 2 X 2 factorial involving pretreatment with sesame oil (SO) or estradiol valerate (5 mg; EV) injected on Days 11 through 14 of the estrous cycle and an intrauterine injection of saline (5 ml; SA) or prostaglandin F2 alpha (50 micrograms; PGF) on Day 14. Peripheral blood samples were collected for 120 min postinjection and analyzed for 15-keto-13,14-dihydro-PGF2 alpha (PGFM). PGFM concentrations were lower in EV than SO gilts (438 vs. 844 pg/ml; p less than 0.05). There was heterogeneity of regression between EV and SO gilts (p less than 0.01), with EV gilts having a slower release of PGF from the uterine lumen into the vasculature. Prostaglandin F2 alpha did not increase mean PGFM concentrations (p greater than 0.10), but resulted in an altered temporal pattern of PGFM (p less than 0.05) compared to SA gilts. There was an interaction between the two treatments over time, with EV-PGF gilts demonstrating a slower, more gradual release of PGFM than SO-PGF gilts. To test whether prostaglandins of the E series were involved in this mechanism, gilts were assigned to two 4 X 4 latin squares balanced for residual effects and treated with saline or flunixen meglumine (Banamine). Each gilt was treated with four PGE:PGF infusion sequences (SEQ) in each uterine horn: phosphate-buffered saline (PBS; PBS-SEQ), PGE1 (50 micrograms), PGE2 (50 micrograms), and PGE1 (25 micrograms) + PGE2 (25 micrograms) (PGE-SEQ), with each infusion followed 15 min later by PGF (25 micrograms).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为验证猪妊娠母体识别的内分泌-外分泌理论,将16头后备母猪随机分配至一个2×2析因设计中,该设计涉及在发情周期的第11至14天用芝麻油(SO)或戊酸雌二醇(5毫克;EV)进行预处理,并在第14天进行子宫内注射生理盐水(5毫升;SA)或前列腺素F2α(50微克;PGF)。注射后120分钟采集外周血样本,分析15-酮-13,14-二氢-PGF2α(PGFM)。EV组后备母猪的PGFM浓度低于SO组(438对844皮克/毫升;p<0.05)。EV组和SO组后备母猪之间存在回归异质性(p<0.01),EV组后备母猪的PGF从子宫腔向血管系统的释放较慢。前列腺素F2α未增加平均PGFM浓度(p>0.10),但与SA组后备母猪相比,导致PGFM的时间模式改变(p<0.05)。两种处理随时间存在交互作用,EV-PGF组后备母猪的PGFM释放比SO-PGF组后备母猪更慢、更渐进。为测试E系列前列腺素是否参与该机制,将后备母猪分配至两个4×4拉丁方,平衡残留效应,并分别用生理盐水或氟尼辛葡甲胺(Banamine)处理。每头后备母猪在每个子宫角接受四种PGE:PGF输注序列(SEQ):磷酸盐缓冲盐水(PBS;PBS-SEQ)、PGE1(50微克)、PGE2(50微克)以及PGE1(25微克)+PGE2(25微克)(PGE-SEQ),每次输注15分钟后接着注射PGF(25微克)。(摘要截断于250字)

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