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未酰化 ghrelin 和 obestatin 对人黄体细胞功能的体外影响。

In vitro effect of unacylated ghrelin and obestatin on human luteal cell function.

机构信息

Cattedra di Fisiopatologia della Riproduzione Umana, Università Cattolica del Sacro Cuore, Rome, Italy.

出版信息

Fertil Steril. 2012 Apr;97(4):991-6. doi: 10.1016/j.fertnstert.2012.01.096. Epub 2012 Jan 29.

DOI:10.1016/j.fertnstert.2012.01.096
PMID:22285751
Abstract

OBJECTIVE

To evaluate whether unacylated ghrelin and obestatin were able to influence human luteal cell function. The effect of these two ghrelin-related peptides on progesterone (P4), prostaglandin (PG) F(2α), PGE(2), and vascular endothelial growth factor (VEGF) release and on VEGF expression in isolated human steroidogenic cells has been investigated.

DESIGN

Prospective laboratory study.

SETTING

University hospital.

PATIENT(S): Corpora lutea were obtained from 23 normally menstruating patients in the midluteal phase of the menstrual cycle.

INTERVENTION(S): Human luteal cells were isolated from corpora lutea, and primary cultures were established.

MAIN OUTCOME MEASURE(S): P4 and PGs release was assayed by enzyme immunoassay, VEGF secretion by ELISA, and VEGF mRNA expression by real-time polymerase chain reaction.

RESULT(S): P4 and VEGF release were significantly reduced by both unacylated ghrelin and obestatin. Moreover, the highest concentration of obestatin was able to reduce the release of PGE(2) and PGF(2α). VEGF mRNA expression was not affected by the incubation with any of these ghrelin-related peptides. As expected, CoCl(2) was able to induce VEGF release and mRNA expression in luteal cells.

CONCLUSION(S): Our results suggest that, similar to ghrelin, both unacylated ghrelin and obestatin might play a role in regulating the luteal cell function that affects both luteal steroidogenesis and luteotrophic/luteolytic imbalance. These results further underline the pivotal correlation between the ghrelin system and reproduction.

摘要

目的

评估酰化 ghrelin 和 obestatin 是否能够影响人黄体细胞功能。研究了这两种 ghrelin 相关肽对孕激素 (P4)、前列腺素 (PG) F2α、PGE2 和血管内皮生长因子 (VEGF) 释放的影响,以及它们对分离的人甾体生成细胞中 VEGF 表达的影响。

设计

前瞻性实验室研究。

设置

大学医院。

患者

从 23 名正常月经周期中期的患者的黄体中获得黄体。

干预

从黄体中分离出人黄体细胞,并建立原代培养。

主要观察指标

通过酶联免疫吸附试验测定 P4 和 PGs 的释放,通过 ELISA 测定 VEGF 的分泌,通过实时聚合酶链反应测定 VEGF mRNA 的表达。

结果

酰化 ghrelin 和 obestatin 均可显著减少 P4 和 VEGF 的释放。此外,最高浓度的 obestatin 能够减少 PGE2 和 PGF2α 的释放。这些 ghrelin 相关肽的孵育并不影响 VEGF mRNA 的表达。正如预期的那样,CoCl2 能够诱导黄体细胞中 VEGF 的释放和 mRNA 的表达。

结论

我们的研究结果表明,与 ghrelin 相似,酰化 ghrelin 和 obestatin 可能在调节黄体细胞功能方面发挥作用,影响黄体甾体生成和黄体营养/黄体溶解的失衡。这些结果进一步强调了 ghrelin 系统与生殖之间的重要相关性。

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