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促性腺激素释放激素刺激大鼠垂体前叶组织中肌醇磷酸的形成。

Gonadotropin releasing hormone stimulates the formation of inositol phosphates in rat anterior pituitary tissue.

作者信息

Schrey M P

出版信息

Biochem J. 1985 Mar 1;226(2):563-9. doi: 10.1042/bj2260563.

Abstract

The production of inositol phosphates in response to gonadotropin releasing hormone (GnRH) was studied in rat anterior pituitary tissue preincubated with [3H]inositol. Prelabelled paired hemipituitaries from prepubertal female rats were incubated in the presence or absence of GnRH in medium containing 10 mM-Li+ X Li+, which inhibits myo-inositol-1-phosphatase, greatly amplified the stimulation of inositol phosphate production by GnRH (10(-7) M) to 159, 198 and 313% of paired control values for inositol 1-phosphate, inositol bisphosphate and inositol trisphosphate respectively after 20 min. The percentage distribution of [3H]inositol within the phosphoinositides was 91.3, 6.3 and 2.4 for phosphatidylinositol, phosphatidylinositol 4-phosphate and phosphatidylinositol 4,5-bisphosphate respectively and was unaffected by GnRH. The stimulation of inositol trisphosphate production by GnRH was evident after 5 min incubation, was dose-dependent with a half-maximal effect around 11 nM, and was not inhibited by removal of extracellular Ca2+. Elevation of cytosolic Ca2+ by membrane depolarization with 50 mM-K+ had no significant effect on inositol phosphate production. These findings are consistent with the hypothesis that GnRH action in the anterior pituitary involves the hydrolysis of phosphatidylinositol 4,5-bisphosphate. The resulting elevation of inositol trisphosphate may in turn lead to intracellular Ca2+ mobilization and subsequent stimulation of gonadotropin secretion.

摘要

用[3H]肌醇预孵育大鼠垂体前叶组织,研究促性腺激素释放激素(GnRH)刺激下肌醇磷酸的生成。将青春期前雌性大鼠预先标记的成对半垂体,在含有10 mM-Li+的培养基中,于有无GnRH的情况下进行孵育。Li+可抑制肌醇-1-磷酸酶,能极大增强GnRH(10(-7) M)对肌醇磷酸生成的刺激作用。孵育20分钟后,与成对对照值相比,肌醇一磷酸、肌醇二磷酸和肌醇三磷酸分别增加到159%、198%和313%。[3H]肌醇在磷脂酰肌醇、磷脂酰肌醇4-磷酸和磷脂酰肌醇4,5-二磷酸中的分布百分比分别为91.3%、6.3%和2.4%,且不受GnRH影响。孵育5分钟后,GnRH对肌醇三磷酸生成的刺激作用明显,呈剂量依赖性,半数最大效应约为11 nM,且不受细胞外Ca2+去除的抑制。用50 mM-K+使细胞膜去极化从而升高胞质Ca2+,对肌醇磷酸的生成无显著影响。这些发现与以下假设一致:GnRH在垂体前叶的作用涉及磷脂酰肌醇4,5-二磷酸的水解。由此导致的肌醇三磷酸升高可能进而引起细胞内Ca2+动员,并随后刺激促性腺激素分泌。

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本文引用的文献

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LHRH rapidly stimulates phosphatidylinositol metabolism in enriched gonadotrophs.
Mol Cell Endocrinol. 1984 Jul;36(3):157-64. doi: 10.1016/0303-7207(84)90031-5.

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