Nilsson K O
Acta Endocrinol (Copenh). 1975 Oct;80(2):230-6. doi: 10.1530/acta.0.0800230.
Six healthy adult males were studied to evaluate the effect of apomorphine on growth hormone (GH) secretion under normoglycaemic and hyperglycaemic conditions. Both under normoglycaemia and hyperglycaemia all subjects responded to the subcutaneous injection of 0.75 mg apomorphine hydrochloride with a marked increase in plasma GH concentration reaching a maximum after 30-60 min. In control studies no significant changes in plasma GH were observed following the injection of physiological saline. As apomorphine is considered a selective dopamine receptor stimulating agent, the results support the view that GH release in man can be modulated through a dopaminergic mechanism. The finding that the plasma GH rise after the administration of apomorphine is not suppressible by glucose indicates that apomorphine activates dopaminergic receptors localized distally in the hypothalamus or in the anterior pituitary. Amorphine in low dosage may be used clinically to test the capacity of the pituitary to release GH in man, at least in special cases.
对6名健康成年男性进行了研究,以评估阿扑吗啡在正常血糖和高血糖条件下对生长激素(GH)分泌的影响。在正常血糖和高血糖情况下,所有受试者皮下注射0.75毫克盐酸阿扑吗啡后,血浆GH浓度均显著升高,在30 - 60分钟后达到峰值。在对照研究中,注射生理盐水后血浆GH未观察到显著变化。由于阿扑吗啡被认为是一种选择性多巴胺受体刺激剂,这些结果支持了人类GH释放可通过多巴胺能机制调节的观点。给予阿扑吗啡后血浆GH升高不受葡萄糖抑制的发现表明,阿扑吗啡激活了位于下丘脑远端或垂体前叶的多巴胺能受体。低剂量的阿扑吗啡至少在特殊情况下可用于临床检测人体垂体释放GH的能力。