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阿托品对人生长激素释放激素诱导的生长激素分泌的阻断作用并非在垂体水平发挥。

Atropine blockade of growth hormone (GH)-releasing hormone-induced GH secretion in man is not exerted at pituitary level.

作者信息

Casanueva F F, Villanueva L, Dieguez C, Cabranes J A, Diaz Y, Szoke B, Scanlon M F, Schally A V, Fernandez-Cruz A

出版信息

J Clin Endocrinol Metab. 1986 Jan;62(1):186-91. doi: 10.1210/jcem-62-1-186.

Abstract

The role of acetylcholine (Ach) in the regulation of human GH secretion was assessed using atropine, which selectively blocks cholinergic muscarinic receptors. Paired tests were performed in seven normal subjects using GH-releasing hormone (GHRH) 1-44 (1 microgram/kg iv), with and without atropine pretreatment (1 mg im). The GHRH 1-44-induced GH secretory peak [20.7 +/- 4.5 (SEM) ng/ml] was completely blocked by atropine administration (2.3 +/- 0.6 ng/ml) (P less than 0.01). To determine whether this atropine blockade was at the pituitary level, a series of in vitro studies were conducted using monolayer cultures of cells from bovine anterior pituitary glands. GHRH 1-44 (10(-8) M) stimulated bovine GH release (11.1 +/- 1.5 micrograms/ml) as compared to control values (5.1 +/- 0.4 microgram/ml) (P less than 0.01). This response was not altered by 10(-6) M atropine (14.9 +/- 0.9 microgram/ml). Similar results were obtained with GHRH, 10(-9) M, with or without atropine, 10(-7) M. Addition of 10(-6) M Ach to the incubation medium significantly increased bovine GH release (12.7 +/- 1.2 microgram/ml) and the effect of 10(-6) M Ach and 10(-8) M GHRH was additive (20.9 +/- 2.1 micrograms/ml) (P less than 0.01). Similar results were obtained with Ach, 10(-5) M, and GHRH, 10(-9) M. Atropine or eserine alone did not alter basal GH secretion, and atropine blocked Ach-stimulating activity. In conclusion, atropine blockade of GHRH-induced GH secretion appears to be exerted at a site other than pituitary.

摘要

使用选择性阻断胆碱能毒蕈碱受体的阿托品,评估乙酰胆碱(Ach)在调节人体生长激素(GH)分泌中的作用。对7名正常受试者进行配对试验,静脉注射生长激素释放激素(GHRH)1 - 44(1微克/千克),分别在有和没有阿托品预处理(肌肉注射1毫克)的情况下进行。GHRH 1 - 44诱导的GH分泌峰值[20.7±4.5(SEM)纳克/毫升]在给予阿托品后完全被阻断(2.3±0.6纳克/毫升)(P<0.01)。为了确定这种阿托品阻断作用是否在垂体水平,使用来自牛垂体前叶细胞的单层培养物进行了一系列体外研究。与对照值(5.1±0.4微克/毫升)相比,GHRH 1 - 44(10⁻⁸摩尔)刺激牛GH释放(11.1±1.5微克/毫升)(P<0.01)。这种反应不受10⁻⁶摩尔阿托品(14.9±0.9微克/毫升)的影响。对于10⁻⁹摩尔GHRH,无论有无10⁻⁷摩尔阿托品,都得到了类似的结果。向孵育培养基中添加10⁻⁶摩尔Ach可显著增加牛GH释放(12.7±1.2微克/毫升),并且10⁻⁶摩尔Ach和10⁻⁸摩尔GHRH的作用是相加的(20.9±2.1微克/毫升)(P<0.01)。对于10⁻⁵摩尔Ach和10⁻⁹摩尔GHRH,也得到了类似的结果。单独使用阿托品或毒扁豆碱不会改变基础GH分泌,并且阿托品可阻断Ach的刺激活性。总之,阿托品对GHRH诱导的GH分泌的阻断作用似乎是在垂体以外的部位发挥的。

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