Kallio A, Koulu M, Scheinin H, Viikari J, Scheinin M
Department of Pharmacology, University of Turku, Finland.
Acta Endocrinol (Copenh). 1988 Sep;119(1):11-5. doi: 10.1530/acta.0.1190011.
Single iv doses (25, 50 and 100 micrograms) of medetomidine, a selective alpha 2-adrenoceptor agonist of the imidazole type, were administered to 8 healthy male volunteers in a randomized, double-blind, placebo-controlled study. The concentration of hGH in plasma was powerfully and dose-dependently increased. The plasma level of cortisol was dose-dependently decreased, whereas TSH showed a slight but statistically significant increase. Plasma levels of PRL, FSH and LH were unaffected by the drug. Medetomidine appears to resemble other alpha 2-adrenoceptor agonists, notably clonidine, in its endocrine effects. Its high selectivity and short duration of action make it a suitable tool for studies of the physiology and pharmacology of alpha 2-adrenoceptors in man.
在一项随机、双盲、安慰剂对照研究中,向8名健康男性志愿者静脉注射了单剂量(25、50和100微克)的咪达唑仑,它是一种咪唑类选择性α2肾上腺素能受体激动剂。血浆中hGH的浓度显著且呈剂量依赖性增加。皮质醇的血浆水平呈剂量依赖性降低,而促甲状腺激素显示出轻微但具有统计学意义的增加。血浆中催乳素、促卵泡激素和促黄体生成素的水平不受该药物影响。咪达唑仑在其内分泌作用方面似乎类似于其他α2肾上腺素能受体激动剂,尤其是可乐定。其高选择性和短作用时间使其成为研究人体α2肾上腺素能受体生理学和药理学的合适工具。