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暴露于外源性促性腺激素释放激素和前列腺素F(2α)后牛黄体的体内和体外反应。

In vivo and in vitro responses of the bovine corpus luteum after exposure to exogenous gonadotropin-releasing hormone and prostaglandin F(2α).

作者信息

Bertrand J E, Stormshak F

机构信息

Department of Biochemistry/Biophysics, Oregon State University, Corvallis, OR.

出版信息

Endocrine. 1996 Apr;4(2):165-73. doi: 10.1007/BF02782761.

Abstract

Administration of gonadotropin-releasing hormone (GnRH) early in the estrous cycle has been shown to cause subsequent altered luteal function. To determine whether membrane-related events may be involved in GnRH-attenuated luteal function, corpora lutea (CL) were removed from beef heifers on day seven of the estrous cycle after iv injection of GnRH or saline on day two of the cycle (n=5/group). Luteal slices were incubated with saline (control), luteinizing hormone (LH), or 8-bromo-cAMP for 2h. In vivo administration of GnRH reduced LH and cAMP-stimulated progesterone production by tissue (p<0.01), but basal progesterone production was not affected (p>0.05). Luteal adenylyl cyclase activity did not differ between saline and GnRH-treated animals (p>0.05). Then to examine if early administration of GnRH alters response of the CL to prostaglandin (PG) F(2α), beefheifers were injected with GnRH as described above (n=4/group), and then injected with PGF(2α) on day eight and the CL removed 60 min later. Blood samples were collected for oxytocin (OT) analysis at frequent intervals after PGF(2α) injection and for progesterone at 0 and 60 min. Induction of the early response gene c-jun or release of OT by PGF(2α) was not altered by GnRH injection (p>0.05). Injection of PGF(2α) decreased serum progesterone by 60 min postinjection (p<0.05), but concentrations of this steroid were unaffected by GnRH (p>0.05). Collectively, these data suggest that GnRH-induced alteration of bovine luteal function may be owing to events distal to cAMP synthesis that do not interfere with PGF(2α)-induced expression of c-jun or OT release, cellular phenomena involved in luteolysis.

摘要

在发情周期早期给予促性腺激素释放激素(GnRH)已被证明会导致随后黄体功能改变。为了确定与膜相关的事件是否可能参与GnRH减弱的黄体功能,在发情周期第2天静脉注射GnRH或生理盐水后,于发情周期第7天从肉牛小母牛身上取出黄体(CL)(每组n = 5)。将黄体切片与生理盐水(对照)、促黄体生成素(LH)或8-溴-cAMP孵育2小时。体内给予GnRH可降低组织中LH和cAMP刺激的孕酮生成(p<0.01),但基础孕酮生成不受影响(p>0.05)。生理盐水处理组和GnRH处理组动物的黄体腺苷酸环化酶活性没有差异(p>0.05)。然后,为了研究早期给予GnRH是否会改变黄体对前列腺素(PG)F2α的反应,按上述方法给肉牛小母牛注射GnRH(每组n = 4),然后在第8天注射PGF2α,60分钟后取出黄体。在注射PGF2α后频繁采集血样用于催产素(OT)分析,并在0和60分钟时采集用于孕酮分析。GnRH注射不会改变PGF2α诱导的早期反应基因c-jun的诱导或OT的释放(p>0.05)。注射PGF2α可使注射后60分钟时血清孕酮降低(p<0.05),但该类固醇的浓度不受GnRH影响(p>0.05)。总体而言,这些数据表明,GnRH诱导的牛黄体功能改变可能是由于cAMP合成远端的事件,这些事件不会干扰PGF2α诱导的c-jun表达或OT释放,而这些细胞现象参与黄体溶解过程。

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