首页> 外文期刊>Prostaglandins and Other Lipid Mediators >Prostaglandin E1 (PGE1), but not prostaglandin E2 (PGE2), alters luteal and endometrial luteinizing hormone (LH) occupied and unoccupied LH receptors and mRNA for LH receptors in ovine luteal tissue to prevent luteolysis.
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Prostaglandin E1 (PGE1), but not prostaglandin E2 (PGE2), alters luteal and endometrial luteinizing hormone (LH) occupied and unoccupied LH receptors and mRNA for LH receptors in ovine luteal tissue to prevent luteolysis.

机译:前列腺素E1(PGE1)而非前列腺素E2(PGE2)会改变绵羊黄体组织中黄体和子宫内膜促黄体生成激素(LH)的占有和未占有LH受体以及LH受体的mRNA,以防止黄体溶解。

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Loss of luteal progesterone secretion at the end of the ovine estrous cycle is via uterine PGF(2)alpha secretion. However, uterine PGF(2)alpha secretion is not decreased during early pregnancy in ewes. Instead, the embryo imparts a resistance to PGF(2)alpha. Prostaglandins E (PGE; PGE(1)+PGE(2)) are increased in endometrium and uterine venous blood during early pregnancy in ewes to prevent luteolysis. Chronic intrauterine infusion of PGE(1) or PGE(2) prevents spontaneous or IUD, estradiol-17beta, or PGF(2)alpha-induced premature luteolysis in nonbred ewes. The objective was to determine whether chronic intrauterine infusion of PGE(1) or PGE(2) affected mRNA for LH receptors, occupied and unoccupied receptors for LH in luteal and caruncular endometrium, and luteal function. Ewes received Vehicle, PGE(1), or PGE(2) every 4h from days 10 to 16 of the estrous cycle via a cathether installed in the uterine lumen ipsilateral to the luteal-containing ovary. Jugular venous blood was collected daily for analysis of progesterone and uterine venous blood was collected on day-16 for analysis of PGF(2)alpha and PGE. Corpora lutea and caruncular endometrium were collected from day-10 preluteolytic control ewes and day-16 ewes treated with Vehicle, PGE(1) or PGE(2) for analysis of the mRNA for LH receptors and occupied and unoccupied receptors for LH. Luteal weights on day-16 in ewes treated with PGE(1) or PGE(2) and day-10 control ewes were similar (P>or=0.05), but were greater (PPGE(2)>Vehicle-treated ewes. Concentrations of PGF(2)alpha and PGE in uterine venous plasma on day-16 were similar (P>or=0.05) in the three treatment groups. Luteal mRNA for LH receptors and unoccupied and occupied LH receptors were similar (P>or=0.05) in day-10 control ewes and day-16 ewes treated with PGE(2) and were lower (P
机译:在绵羊发情周期结​​束时黄体孕酮分泌的丢失是通过子宫PGF(2)alpha分泌引起的。但是,子宫PGF(2)alpha分泌不会减少早期妊娠母羊。而是,胚胎赋予对PGF(2)alpha的抵抗力。在母羊早期妊娠期间,子宫内膜和子宫静脉血中的前列腺素E(PGE; PGE(1)+ PGE(2))增多,以防止黄体溶解。长期宫内输注PGE(1)或PGE(2)可防止非繁殖母羊自发或宫内节育器,雌二醇-17β或PGF(2)α诱导的过早黄体溶解。目的是确定宫内输注PGE(1)或PGE(2)是否会影响LH受体的mRNA,黄体和黄体子宫内膜LH的占有和未占用受体以及黄体功能。从动情周期的第10天到第16天,母羊每隔4小时通过安装在含黄体卵巢同侧子宫腔中的导管接受车辆,PGE(1)或PGE(2)。每天收集颈静脉血用于孕酮分析,并在第16天收集子宫静脉血用于PGF(2)alpha和PGE分析。从接受溶媒,PGE(1)或PGE(2)处理的第10天黄体溶解前对照母羊和第16天母羊中收集黄体和绒毛膜内膜,以分析LH受体的mRNA和LH受体的未占用。用PGE(1)或PGE(2)处理的母羊和第10天的对照母羊在第16天的黄体重相似(P> = 0.05),但比第16天更大(P <或= 0.05)车辆处理过的母羊。各治疗组之间第10至16天的孕酮谱有差异(P <或= 0.05):PGE(1)> PGE(2)>经车辆处理的母羊。在三个治疗组中,第16天子宫静脉血浆中PGF(2)α和PGE的浓度相似(P>或= 0.05)。在PGE(2)处理的第10天对照母羊和第16天母羊中,LH受体和未占用和占用的LH受体的促黄体mRNA相似(P> or = 0.05),而在PGE(2)处理后较低。 16车辆处理过的母羊。 PGE(2)防止LH受体以及被占领和未被占领的LH受体第16天黄体mRNA丢失(P <或= 0.05)。在接受PGE(1)处理的母羊的第16天,LH受体的黄体和食管组织mRNA以及被占领和未被占领的LH受体的mRNA均高于任何处理组(P <或= 0.05)。在第16天接受媒介物或PGE(2)处理的母羊中,与第10天对照母羊相比,在棒状体中LH受体和LH的占有和未占有受体的mRNA更大(P <或= 0.05)。结论是PGE(1)和PGE(2)具有一些共同的防止黄体溶解的机制。然而,只有PGE(1)增加了LH受体的黄体和子宫内膜mRNA以及LH受体的占有和未占有。 PGE(2)可防止LH受体的黄体mRNA和LH的被占领和未被占用的受体减少,而不会改变LH受体的子宫内膜mRNA或LH的被占领和未被占用的受体。

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