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大鼠生长激素释放因子刺激正中隆起中环状鸟苷酸的形成和磷脂酰肌醇代谢。

Rat growth hormone-releasing factor stimulates cyclic GMP formation and phosphatidylinositol metabolism in the median eminence.

作者信息

Aguila M C, Snyder G D, McCann S M

机构信息

Department of Physiology, University of Texas Southwestern Medical Center, Dallas 75235-9040.

出版信息

Life Sci. 1991;49(1):67-74. doi: 10.1016/0024-3205(91)90580-5.

Abstract

The effects of rat growth hormone releasing factor (rGRF) on somatostatin (SRIF) secretion, cyclic nucleotide production and phosphatidylinositol metabolism were investigated in the median eminence (ME), using an in vitro system. Medium was discarded and replaced by medium containing various concentrations of rGRF or rGRF plus epinephrine (E, 6 x 10(-7) M). rGRF had no effect on basal or E-stimulated release of cAMP. In the same experiments rGRF markedly stimulated SRIF release. These results suggested that cAMP is not involved in the stimulatory effect of GRF on SRIF release. However, GRF significantly stimulated release of both SRIF and cGMP in a dose-related manner. Maximal stimulation was observed at 10(-10) M GRF (p less than 0.005) which also produces maximal SRIF release. 2'0-monobutyrylguanosine 3'5' cyclic phosphate (mbcGMP, 10(-11) to 10(-10) M) stimulated SRIF release from ME fragments (p less than 0.001 at 10(-10) M) whereas the control, sodium butyrate (10(-6) M), had no effect. GRF caused significant elevation of 30.6% in the concentration of labelled inositol phosphates [( 3H]-IPs) in the ME. These data indicate that GRF stimulation of SRIF release is accompanied by increased cGMP production and phosphatidyl-inositol (PI) metabolism but does not alter cAMP production. Because mbcGMP can directly stimulate SRIF release, we suggest that GRF causes a receptor-mediated increase in the metabolism of phosphatidylinositol and cGMP formation. These actions therefore may be among the early metabolic events in the mechanism of GRF-stimulated SRIF release from the ME.

摘要

利用体外系统,研究了大鼠生长激素释放因子(rGRF)对正中隆起(ME)中生长抑素(SRIF)分泌、环核苷酸生成及磷脂酰肌醇代谢的影响。弃去培养基,代之以含有不同浓度rGRF或rGRF加肾上腺素(E,6×10⁻⁷M)的培养基。rGRF对基础或E刺激的cAMP释放无影响。在相同实验中,rGRF显著刺激SRIF释放。这些结果提示,cAMP不参与GRF对SRIF释放的刺激作用。然而,GRF以剂量相关方式显著刺激SRIF和cGMP的释放。在10⁻¹⁰M GRF时观察到最大刺激(p<0.005),此时也产生最大SRIF释放。2′,0-单丁酰鸟苷3′,5′环磷酸酯(mbcGMP,10⁻¹¹至10⁻¹⁰M)刺激ME片段释放SRIF(10⁻¹⁰M时p<0.001),而对照丁酸钠(10⁻⁶M)无作用。GRF使ME中标记的肌醇磷酸酯[(³H]-IPs)浓度显著升高30.6%。这些数据表明,GRF刺激SRIF释放伴随着cGMP生成增加和磷脂酰肌醇(PI)代谢增加,但不改变cAMP生成。由于mbcGMP可直接刺激SRIF释放,我们认为GRF导致受体介导的磷脂酰肌醇代谢增加和cGMP形成增加。因此,这些作用可能是GRF刺激ME释放SRIF机制中的早期代谢事件之一。

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