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首页> 外文期刊>Czech Journal of Animal Science >Peroxisome proliferator activated receptor ligands affect porcine endometrial steroids production during the estrous cycle and early pregnancy: an in vitro study
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Peroxisome proliferator activated receptor ligands affect porcine endometrial steroids production during the estrous cycle and early pregnancy: an in vitro study

机译:过氧化物酶体增殖物激活的受体配体在动情周期和怀孕初期影响猪子宫内膜类固醇的产生:一项体外研究

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摘要

In the present study, we investigated the effect of PPAR ligands on progesterone (P4) and 17β-estradiol (E2) secretion, as well as 3β-hydroxysteroid dehydrogenase/Δ(5)-Δ(4) isomerase (3β-HSD) mRNA expression, in porcine endometrial slices collected on days 10–12 and 14–16 of the estrous cycle or early pregnancy. The explants were incubated in vitro for 6 h in the presence of PPARα ligands – WY-14643 (agonist) and MK 886 (antagonist); PPARβ ligands – L-165041 (agonist) and GW 9662 (antagonist); PPARγ ligands – 15d-prostaglandin J2 and rosiglitazone (agonists) and T0070907 (antagonist). During the estrous cycle, all PPAR ligands inhibited P4 secretion during the mid-luteal phase (days 10–12). During early pregnancy, a stimulatory effect of PPARα agonist was observed during maternal recognition of pregnancy (days 10–12), while an inhibitory effect was observed at the beginning of implantation (days 14–16). PPAR ligands inhibited the expression of 3β-HSD mRNA on days 14–16 of the estrous cycle (β and γ isoforms) or pregnancy (α, β, γ isoforms) but did not affect gene expression on days 10–12 of the estrous cycle or early pregnancy. An inhibitory effect of PPARα, PPARγ, and PPARβ on E2 secretion was observed during maternal recognition of pregnancy, but a stimulatory effect was observed during mid- (γ isoform) or late-luteal (β isoform) phases of the estrous cycle. Our study indicates, for the first time, that PPARs are engaged in P4 and E2 production in porcine endometrium. It is possible that the diverse receptivity of endometrial tissue to the PPAR ligands can be associated with the reproductive status of gilts.
机译:在本研究中,我们研究了PPAR配体对孕酮(P 4 )和17β-雌二醇(E 2 )分泌以及3β-羟基类固醇脱氢酶/ Δ(5)-Δ(4)异构酶(3β-HSD)mRNA表达,在动情周期或怀孕初期第10-12天和14-16天收集的猪子宫内膜切片中。外植体在PPARα配体WY-14643(激动剂)和MK 886(拮抗剂)存在下体外孵育6小时。 PPARβ配体– L-165041(激动剂)和GW 9662(拮抗剂); PPARγ配体– 15d-前列腺素J 2 和罗格列酮(激动剂)和T0070907(拮抗剂)。在发情周期中,所有PPAR配体在黄体中期(第10-12天)均抑制P 4 分泌。在怀孕早期,在孕妇识别怀孕期间(第10-12天)观察到PPARα激动剂有刺激作用,而在植入开始时(第14-16天)观察到有抑制作用。 PPAR配体在发情周期的14–16天(β和γ亚型)或妊娠(α,β,γ异构体)抑制3β-HSDmRNA的表达,但在发情周期的10–12天不影响基因表达。或早孕。在母体识别怀孕期间观察到PPARα,PPARγ和PPARβ对E 2 分泌的抑制作用,但在中(γ亚型)或黄体后期(β亚型)中观察到刺激作用。发情周期的各个阶段。我们的研究首次表明,PPAR参与了猪子宫内膜的P 4 和E 2 生产。子宫内膜组织对PPAR配体的不同接受可能与后备母猪的生殖状态有关。

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