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多潘立酮对正常男性阿扑吗啡诱导的生长激素分泌的影响。

Effect of domperidone on apomorphine-induced growth hormone secretion in normal men.

作者信息

Lal S, Nair N P, Iskandar H L, Etienne P, Wood P L, Schwartz G, Guyda H

出版信息

J Neural Transm. 1982;54(1-2):75-84. doi: 10.1007/BF01249280.

Abstract

Domperidone, a peripheral dopamine (DA) receptor blocker which poorly crosses the blood-brain barrier and which is inactive towards dopamine-sensitive adenylate cyclase, in a dose (100 micrograms/kg) sufficient to increase serum prolactin levels at least 5-fold, decreased the growth hormone (GH) response to the DA receptor agonist, apomorphine HCI (Apo) (0.5 gm s.c.) in each of six normal men examined. The mean GH increment at 30, 45, 60 and 75 min following Apo injection, the mean individual peak increment and the mean individual GH secretion (ng min) was significantly decreased by domperidone pretreatment (p less than 0.005 -p less than 0.002). These results indicate that in man Apo stimulates GH secretion by an effect on DA receptors which are not linked to adenylate cyclase and which are situated at a locus in the hypothalamic-pituitary axis that lies outside the blood-brain barrier.

摘要

多潘立酮是一种外周多巴胺(DA)受体阻滞剂,它很难穿过血脑屏障,且对多巴胺敏感的腺苷酸环化酶无活性。在六名接受检查的正常男性中,多潘立酮以足以使血清催乳素水平至少升高5倍的剂量(100微克/千克),降低了生长激素(GH)对DA受体激动剂盐酸阿扑吗啡(Apo)(0.5克皮下注射)的反应。多潘立酮预处理显著降低了Apo注射后30、45、60和75分钟时的平均GH增加值、平均个体峰值增加值以及平均个体GH分泌量(纳克/分钟)(p小于0.005 - p小于0.002)。这些结果表明,在人类中,Apo通过作用于与腺苷酸环化酶不相关且位于血脑屏障外的下丘脑 - 垂体轴位点的DA受体来刺激GH分泌。

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