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[垂体腺苷酸环化酶激活多肽mRNA在妊娠大鼠黄体中的表达与调控]

[Expression and regulation of pituitary adenylate cyclase-activating polypeptide mRNA in pregnant rat corpus luteum].

作者信息

Zhao Wei, Cheng Dan-Ling, Zheng Hui-Li, Zhu Hui, Ni Jiang

机构信息

Department of Physiology, Harbin Medical University, Harbin 150086, China.

出版信息

Zhongguo Ying Yong Sheng Li Xue Za Zhi. 2010 Aug;26(3):313-7.

Abstract

OBJECTIVE

To investigate the expression changes and regulation of pituitary adenylate cyclase-activating polypeptide (PACAP) mRNA in corpus luteum during pregnancy.

METHODS

Pregnant rats' ovaries were collected at different time points. The techniques of RT-PCR and in situ hybridization were used to observe expression changes of PACAP mRNA in rat ovaries during pregnancy. To further explore the regulation mechanism of PACAP mRNA expression in corpus luteum, luteal cells were cultured in vitro. Immature (25 - 28 days old) female Sprague-Dawley rats were injected subcutaneously with 50IU pregnant mare serum gonadotrophin (PMSG), and 25IU human chorionic gonadotrophin (hCG) 48 h later, to induce follicular development and luteum formation. On day 6 after hCG administration (the day of hCG administration was the first day), the rats were killed by guillotine and the ovarian luteal cells were collected. After incubation for 24 h, luteal cells were administration with various factors for 24 h. And then expression changes of PACAP mRNA in luteal cells after administration with different factors were detected by RT-PCR, and radioimmunoassay was used to analyze progesterone levels.

RESULTS

With the development of pregnancy, the expression of PACAP mRNA increased gradually, reached the peak at pregnancy 19 d, and then decreased. Compared with control group, platelet activating factor (PAF), forskolin and PMA could obviously stimulate PACAP mRNA expression in luteal cells which were cultured with corresponding factors for 24 h. At the same time, progesterone levels in culture media were also elevated.

CONCLUSION

PACAP, acting as a local ovary regulator, was closely related to the maintenance of medium-term and late pregnancy. PAF could directly stimulate PACAP mRNA expression in luteal cells, and protein kinase C (PKC) and protein kinase A (PKA) signal pathways could both participate in this process.

摘要

目的

研究孕期黄体中垂体腺苷酸环化酶激活多肽(PACAP)mRNA的表达变化及调控机制。

方法

在不同时间点收集妊娠大鼠的卵巢。采用逆转录-聚合酶链反应(RT-PCR)和原位杂交技术观察孕期大鼠卵巢中PACAP mRNA的表达变化。为进一步探讨黄体中PACAP mRNA表达的调控机制,进行体外培养黄体细胞。选用未成熟(25 - 28日龄)雌性Sprague-Dawley大鼠,皮下注射50IU孕马血清促性腺激素(PMSG),48小时后再注射25IU人绒毛膜促性腺激素(hCG),以诱导卵泡发育和黄体形成。在注射hCG后第6天(注射hCG当天为第1天),断头处死大鼠并收集卵巢黄体细胞。培养24小时后,用各种因子处理黄体细胞24小时。然后通过RT-PCR检测不同因子处理后黄体细胞中PACAP mRNA的表达变化,并用放射免疫分析法分析孕酮水平。

结果

随着孕期的发展,PACAP mRNA的表达逐渐增加,在妊娠19天时达到峰值,随后下降。与对照组相比,血小板活化因子(PAF)、福斯高林和佛波酯(PMA)能明显刺激用相应因子培养24小时的黄体细胞中PACAP mRNA的表达。同时,培养基中的孕酮水平也升高。

结论

PACAP作为一种局部卵巢调节因子,与妊娠中晚期的维持密切相关。PAF可直接刺激黄体细胞中PACAP mRNA的表达,蛋白激酶C(PKC)和蛋白激酶A(PKA)信号通路均参与此过程。

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