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生长激素释放激素刺激体外灌流大鼠垂体细胞释放环磷酸腺苷。

Growth hormone-releasing hormone stimulates cAMP release in superfused rat pituitary cells.

作者信息

Horváth J E, Groot K, Schally A V

机构信息

Endocrine, Polypeptide and Cancer Institute, New Orleans, LA.

出版信息

Proc Natl Acad Sci U S A. 1995 Mar 14;92(6):1856-60. doi: 10.1073/pnas.92.6.1856.

Abstract

The release of growth hormone (GH) and cAMP was studied in superfused rat pituitary cells by infusing growth hormone-releasing hormone (GHRH) at different doses or a combination of GHRH and somatostatin 14 (SS-14). Three-minute pulses of GHRH caused a dose-dependent GH and cAMP release (effective concentration of 50% of the maximal biological effect is 0.21 nM and 52.5 nM, respectively). The lowest effective doses of GHRH in the superfusion system were 0.03 nM for GH release and 0.3 nM for cAMP discharge when 3-min pulses were applied. The amount of cAMP liberated from the cells was not proportional to GH release: cAMP responses to low doses of GHRH were disproportionally small, and the gradual increase in the release of cAMP after high doses of GHRH was not followed by a parallel rise in GH release. The desensitization induced by repeated pulses or prolonged infusion of GHRH resulted in a greater reduction in GH release than in cAMP liberation. A simultaneous infusion of SS-14 completely blocked GH release stimulated by GHRH but did not inhibit the immediate release of cAMP caused by GHRH. An abrupt decrease in GHRH-stimulated GH release induced by SS-14 was followed by only a minimal reduction in cAMP liberation 9 min later. Our findings indicate that a discharge of cAMP is stimulated after a GHRH pulse, but this effect alone cannot maintain the release of GH. Other steps of the signal transduction mechanisms that are independent of the cAMP route may participate in the process of GH release. The nature of the mechanisms involved in the mediation of GH release may vary with the doses of GHRH used.

摘要

通过以不同剂量注入生长激素释放激素(GHRH)或GHRH与生长抑素14(SS - 14)的组合,研究了在体外灌流的大鼠垂体细胞中生长激素(GH)和环磷酸腺苷(cAMP)的释放情况。GHRH的三分钟脉冲导致了剂量依赖性的GH和cAMP释放(最大生物学效应的50%的有效浓度分别为0.21 nM和52.5 nM)。当施加三分钟脉冲时,在灌流系统中GHRH促进GH释放的最低有效剂量为0.03 nM,促进cAMP释放的最低有效剂量为0.3 nM。从细胞中释放的cAMP量与GH释放不成比例:低剂量GHRH引起的cAMP反应过小,而高剂量GHRH后cAMP释放的逐渐增加并未伴随GH释放的平行增加。重复脉冲或长时间注入GHRH引起的脱敏导致GH释放的减少比cAMP释放的减少更大。同时注入SS - 14完全阻断了GHRH刺激的GH释放,但并未抑制GHRH引起的cAMP的即时释放。SS - 14引起的GHRH刺激的GH释放的突然减少之后,9分钟后cAMP释放仅略有减少。我们的研究结果表明,GHRH脉冲后会刺激cAMP释放,但仅这种作用不能维持GH的释放。信号转导机制中与cAMP途径无关的其他步骤可能参与了GH释放过程。参与介导GH释放的机制的性质可能因所用GHRH的剂量而异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e34/42381/dc13362f7f47/pnas01484-0073-a.jpg

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