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首页> 外文期刊>Prostaglandins and Other Lipid Mediators >In vivo intra-luteal implants of prostaglandin (PG) E 1 or E 2 (PGE 1, PGE 2) prevent luteolysis in cows. II: MRNA for PGF 2α, EP1, EP2, EP3 (A-D), EP3A, EP3B, EP3C, EP3D, and EP4 prostanoid receptors in luteal tissue
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In vivo intra-luteal implants of prostaglandin (PG) E 1 or E 2 (PGE 1, PGE 2) prevent luteolysis in cows. II: MRNA for PGF 2α, EP1, EP2, EP3 (A-D), EP3A, EP3B, EP3C, EP3D, and EP4 prostanoid receptors in luteal tissue

机译:体内前列腺素(PG)E 1或E 2(PGE 1,PGE 2)的黄体内植入物可防止母牛的黄体溶解。 II:黄体组织中PGF2α,EP1,EP2,EP3(A-D),EP3A,EP3B,EP3C,EP3D和EP4前列腺素受体的MRNA

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摘要

Previously, it was reported that chronic intra-uterine infusion of PGE 1 or PGE 2 every 4 h inhibited luteolysis in ewes by altering luteal mRNA for luteinizing hormone (LH) receptors and unoccupied and occupied luteal LH receptors. However, estradiol-17β or PGE 2 given intra-uterine every 8 h did not inhibit luteolysis in cows, but infusion of estradiol + PGE 2 inhibited luteolysis. In contrast, intra-luteal implants containing PGE 1 or PGE 2 in Angus or Brahman cows also inhibited the decline in circulating progesterone, mRNA for LH receptors, and loss of unoccupied and occupied receptors for LH to prevent luteolysis. The objective of this experiment was to determine how intra-luteal implants of PGE 1 or PGE 2 alter mRNA for prostanoid receptors and how this could influence luteolysis in Brahman or Angus cows. On day-13 Angus cows received no intra-luteal implant and corpora lutea were retrieved or Angus and Brahman cows received intra-luteal silastic implants containing Vehicle, PGE 1, or PGE 2 and corpora lutea were retrieved on day-19. Corpora lutea slices were analyzed for mRNA for prostanoid receptors (FP, EP1, EP2, EP3 (A-D), EP3A, EP3B, EP3C, EP3D, and EP4) by RT-PCR. Day-13 Angus cow luteal tissue served as pre-luteolytic controls. mRNA for FP receptors decreased in day-19 Vehicle controls compared to day-13 Vehicle controls regardless of breed. PGE 1 and PGE 2 up-regulated FP gene expression on day-19 compared to day-19 Vehicle controls regardless of breed. EP1 mRNA was not altered by any treatment. PGE 1 and PGE 2 down-regulated EP2 and EP4 mRNA compared to day-19 Vehicle controls regardless of breed. PGE 1 or PGE 2 up-regulated mRNA EP3B receptor subtype compared to day-19 Vehicle control cows regardless of breed. The similarities in relative gene expression profiles induced by PGE 1 and PGE 2 support their agonistic effects. We conclude that both PGE 1 and PGE 2 may prevent luteolysis by altering expression of mRNA for prostanoid receptors, which is correlated with changes in luteal mRNA for LH receptors reported previously in these same cows to prevent luteolysis.
机译:以前,有报道说,每隔4小时向子宫内输注PGE 1或PGE 2会通过改变黄体生成激素(LH)受体的黄体mRNA和未占用和占据的黄体LH受体而抑制母羊的黄体溶解。然而,每隔8 h宫内给予雌二醇17β或PGE 2不会抑制母牛的黄体溶解,但是输注雌二醇+ PGE 2会抑制黄体溶解。相比之下,安格斯或婆罗门牛中含有PGE 1或PGE 2的黄体内植入物也抑制循环孕酮的下降,LH受体的mRNA以及LH的未占用和占据的受体的丢失,从而防止黄体溶解。本实验的目的是确定黄体内植入的PGE 1或PGE 2如何改变前列腺素受体的mRNA,以及这如何影响婆罗门或安格斯牛的黄体溶解。在第13天,未接受黄体内植入物的安格斯牛和黄体被取回,或者接受包含媒介物,PGE 1或PGE 2和黄体的黄体内硅质植入物的安格斯和婆罗门牛在第19天被取回。通过RT-PCR分析黄体切片的类前列腺素受体(FP,EP1,EP2,EP3(A-D),EP3A,EP3B,EP3C,EP3D和EP4)的mRNA。第13天安格斯牛黄体组织用作黄体溶解前对照。与第13天的媒介物对照组相比,第19天的媒介物对照组中FP受体的mRNA下降,而与品种无关。与第19天的媒介物对照相比,无论何种品种,PGE 1和PGE 2在第19天上调FP基因表达。 EP1 mRNA没有任何改变。与第19天媒介物对照相比,无论何种品种,PGE 1和PGE 2均下调EP2和EP4 mRNA。与第19天的媒介物对照母牛相比,无论品种如何,PGE 1或PGE 2上调的mRNA EP3B受体亚型。由PGE 1和PGE 2诱导的相对基因表达谱的相似性支持了它们的激动作用。我们得出的结论是,PGE 1和PGE 2均可通过改变前列腺素受体mRNA的表达来预防黄体溶解,这与先前在这些相同母牛中预防黄体溶解的LH受体的黄体mRNA的变化相关。

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