Robinson I C
Division of Neurophysiology, National Institute for Medical Research, London, UK.
Acta Paediatr Suppl. 1997 Nov;423:88-91. doi: 10.1111/j.1651-2227.1997.tb18382.x.
Various novel growth hormone (GH) secretagogues have been developed. GH secretagogues release GH directly from the pituitary via a pathway distinct from that involving GH-releasing hormone (GHRH). However, they also act centrally to activate hypothalamic neurones, and require an intact GHRH system for potent in vivo activity. Both normal and transgenic growth-retarded (Tgr) rats release GH in response to GH secretagogues, and their responses are sensitive to the pattern of secretagogue administration. GH secretagogues are not completely specific for GH release, but also activate the adrenocorticotrophin-adrenal axis, implying that they have additional central actions. The recent cloning of an endogenous receptor for GH secretagogues now makes it possible to identify central targets for their action. An endogenous receptor implies the existence of an endogenous ligand, but its site of production, relationship to the xenobiotic pharmacological agents and its underlying physiological relevance remain unclear.
已经研发出了多种新型生长激素(GH)促分泌素。GH促分泌素通过一条不同于生长激素释放激素(GHRH)的途径直接从垂体释放GH。然而,它们也在中枢发挥作用,激活下丘脑神经元,并且在体内发挥强效活性需要完整的GHRH系统。正常大鼠和转基因生长迟缓(Tgr)大鼠都会对GH促分泌素产生反应而释放GH,并且它们的反应对促分泌素的给药模式敏感。GH促分泌素并非完全特异性地促进GH释放,还会激活促肾上腺皮质激素-肾上腺轴,这意味着它们还有其他中枢作用。最近克隆出了一种GH促分泌素的内源性受体,现在有可能确定其作用的中枢靶点。一种内源性受体意味着存在内源性配体,但其产生部位、与外源性药理制剂的关系及其潜在的生理相关性仍不清楚。