Martin J B, Audet J, Saunders A
Endocrinology. 1975 Apr;96(4):839-47. doi: 10.1210/endo-96-4-839.
Morphine in intravenous doses ranging from 10 mug/kg to 8 mg/kg was shown to be effective in stimulating GH release in the unanesthetized rat. The response to the log of the dose was linear over a range of 10 to 1000 mug/kg. Somatostatin (GH-release inhibiting factor) administered SC in a dose of 200 mug/kg 5 min before morphine prevented the GH rise. Neither inhibitors of catecholamine or serotonin synthesis nor blockage of alpha and beta-adrenergic receptors had any effect on the response. The response was partially blocked in animals with large hypothalamic ventromedial (VMN) lesions. Such lesions completely abolished the GH response to pentobarbital. These results indicate that morphine is a remarkably potent agent for stimulation of GH release but the precise mechanism and site of action of the drug remain to be determined.
静脉注射剂量为10微克/千克至8毫克/千克的吗啡,已被证明能有效刺激未麻醉大鼠的生长激素(GH)释放。在10至1000微克/千克的剂量范围内,对剂量对数的反应呈线性。在注射吗啡前5分钟皮下注射200微克/千克的生长抑素(生长激素释放抑制因子)可阻止生长激素升高。儿茶酚胺或5-羟色胺合成抑制剂以及α和β肾上腺素能受体阻断剂对该反应均无任何影响。在患有大型下丘脑腹内侧核(VMN)损伤的动物中,该反应被部分阻断。此类损伤完全消除了对戊巴比妥的生长激素反应。这些结果表明,吗啡是一种非常有效的生长激素释放刺激剂,但该药物的确切作用机制和作用部位仍有待确定。