Franceschini R, Cataldi A, Garibaldi A, Cianciosi P, Scordamaglia A, Barreca T, Rolandi E
Department of Internal Medicine, n. 6 University of Genoa, Italy.
Neuropharmacology. 1994 Feb;33(2):235-9. doi: 10.1016/0028-3908(94)90014-0.
Sumatriptan, a new antimigraine drug with high affinity and selectivity for certain 5-hydroxytryptamine (5-HT1D) receptor subtypes, was administered to 12 normal subjects, in order to investigate the effects of 5-HT receptor activation on anterior pituitary secretion. Sumatriptan increased plasma growth hormone (GH) levels from 2.5 +/- 0.5 mIU/l in basal conditions to 17.3 +/- 2.6 mIU/l 30 min after administration of the drug. After pre-treatment with cyproheptadine, an anti-serotoninergic drug known to inhibit GH secretion, the mean integrated sumatriptan-induced GH response decreased from 14.8 +/- 3.9 muI/lhr to 3.7 +/- 1.7 mIU/lhr. Sumatriptan administration did not have any effect on the secretion of the other anterior pituitary hormones. It is concluded that sumatriptan selectively increases GH secretion in man, but the exact nature of the receptors involved is not yet known.
舒马曲坦是一种对某些5-羟色胺(5-HT1D)受体亚型具有高亲和力和选择性的新型抗偏头痛药物,为研究5-羟色胺(5-HT)受体激活对垂体前叶分泌的影响,将其给予12名正常受试者。舒马曲坦可使血浆生长激素(GH)水平从基础状态下的2.5±0.5 mIU/L升高至给药后30分钟时的17.3±2.6 mIU/L。在用赛庚啶(一种已知可抑制GH分泌的抗5-羟色胺能药物)预处理后,舒马曲坦诱导的GH平均综合反应从14.8±3.9 μI/L·小时降至3.7±1.7 mIU/L·小时。给予舒马曲坦对其他垂体前叶激素的分泌没有任何影响。得出的结论是,舒马曲坦可选择性增加人体GH分泌,但所涉及受体的确切性质尚不清楚。