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褪黑素和赛庚啶对人生长激素分泌的抑制作用。

Suppression of human growth hormone secretion by melatonin and cyproheptadine.

作者信息

Smythe G A, Lazarus L

出版信息

J Clin Invest. 1974 Jul;54(1):116-21. doi: 10.1172/JCI107732.

Abstract

Pituitary growth hormone (GH) release in the rat is stimulated via serotoninergic pathways and can be inhibited by treatment with compounds that act as serotonin antagonists, such as cyproheptadine or the pineal gland hormone, melatonin. To investigate a possible role for serotonin in the control of human GH release, the effects of cyproheptadine and melatonin administration on the GH responses of normal male subjects were examined. The oral administration of cyproheptadine (8-12 mg daily for 5 days) to normal subjects reduced their GH responses to both insulin-induced hypoglycemia and physical exercise to a highly significant extent. Similarly, the mean GH responses of 10 subjects to insulin-induced hypoglycemia were significantly reduced after the prior oral administration of melatonin (1 g). The data presented show that serotonin antagonism has a similar effect on GH secretion in man to that observed in the rat and provides further evidence for serotoninergic, and possibly pineal, involvement in the control of human GH secretion.

摘要

大鼠垂体生长激素(GH)的释放通过5-羟色胺能途径被刺激,并且可以被作为5-羟色胺拮抗剂的化合物(如赛庚啶或松果体激素褪黑素)的处理所抑制。为了研究5-羟色胺在控制人类GH释放中的可能作用,研究了赛庚啶和褪黑素给药对正常男性受试者GH反应的影响。对正常受试者口服赛庚啶(每天8 - 12毫克,共5天)可使其对胰岛素诱导的低血糖和体育锻炼的GH反应在很大程度上显著降低。同样,10名受试者在预先口服褪黑素(1克)后,对胰岛素诱导的低血糖的平均GH反应也显著降低。所呈现的数据表明,5-羟色胺拮抗作用对人类GH分泌的影响与在大鼠中观察到的相似,并为5-羟色胺能以及可能的松果体参与人类GH分泌的控制提供了进一步的证据。

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