丁螺环酮后血清催乳素水平。

Medical biology Pub Date : 1987-01-01
T Seppälä, T Ranta, R C Shrotriya
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引用次数: 0

摘要

丁螺环酮是一种具有多巴胺(DA)激动剂和拮抗剂混合特性的抗焦虑药(通过阻断突触前和突触后受体实现),对10名健康年轻男性血清催乳素(PRL)的急性影响进行了交叉和双盲试验。舒必利(200 mg)作为对照药物;它将PRL提高了近800%。丁螺环酮(25、50和100 mg)升高血清PRL呈剂量依赖性;每次给药后1小时,最大的增加(分别比基线增加30%、70%和320%)。结果表明丁螺环酮阻断突触后DA受体的剂量仅高于抗焦虑所需的剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum prolactin levels after buspirone in man.

The acute effects of buspirone, an anxiolytic with mixed dopamine (DA) agonist-antagonist properties (achieved by blocking pre- and postsynaptic receptors) on serum prolactin (PRL) were studied in cross-over and double-blind trials in ten healthy young males. Sulpiride (200 mg) was used as a control drug; it raised PRL by almost 800%. Buspirone (25, 50 and 100 mg) raised serum PRL dose-dependently; the greatest increases (30, 70, and 320% from baseline, respectively) were seen 1 h after each dose. The results suggest that buspirone blocks postsynaptic DA receptors only at doses higher than those needed for anxiolysis.

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