Meltzer H Y, Flemming R, Robertson A
Arch Gen Psychiatry. 1983 Oct;40(10):1099-102. doi: 10.1001/archpsyc.1983.01790090061009.
Buspirone hydrochloride, a compound with novel chemical structure, has been reported to be anxiolytic in man. Its mechanism of action as an anxiolytic is unknown, but preclinical studies have shown that it produces effects consistent with both a dopamine agonist and antagonist. In man, buspirone hydrochloride at doses of 30, 60, and 90 mg orally significantly elevated plasma prolactin (PRL) and growth hormone (GH) concentrations. The apparent increase in PRL secretion was dose dependent, but that of GH was not. The increase in PRL secretion could be due to a dopamine antagonist effect at the pituitary gland. A dopamine agonist action at hypothalamic dopamine receptors could account for the increase in GH secretion. Benzodiazepine anxiolytic drugs also increase serum GH levels in man, by a mechanism that has not been clearly established. It may be that buspirone and benzodiazepine drugs stimulate GH secretion by a common mechanism that is related to their anxiolytic actions.
盐酸丁螺环酮是一种具有新型化学结构的化合物,据报道对人体有抗焦虑作用。其作为抗焦虑药的作用机制尚不清楚,但临床前研究表明,它产生的效应与多巴胺激动剂和拮抗剂均相符。在人体中,口服30、60和90毫克剂量的盐酸丁螺环酮可显著提高血浆催乳素(PRL)和生长激素(GH)浓度。PRL分泌的明显增加呈剂量依赖性,而GH则不然。PRL分泌的增加可能是由于垂体处的多巴胺拮抗剂作用。下丘脑多巴胺受体处的多巴胺激动剂作用可能是GH分泌增加的原因。苯二氮䓬类抗焦虑药物也会提高人体血清GH水平,其机制尚未明确。可能是丁螺环酮和苯二氮䓬类药物通过与其抗焦虑作用相关的共同机制刺激GH分泌。