Golden R N, Hsiao J, Lane E, Hicks R, Rogers S, Potter W Z
Department of Psychiatry, University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599.
J Clin Endocrinol Metab. 1989 Mar;68(3):632-7. doi: 10.1210/jcem-68-3-632.
The neuroendocrine effects of iv administration of clomipramine (CMI), a serotonin reuptake inhibitor, were studied in normal subjects. Under double blind, placebo-controlled conditions, single 10- and 20-mg doses of CMI were administered. Ten milligrams of CMI led to significant increases in plasma PRL and cortisol concentrations; plasma ACTH increased slightly but not significantly. In contrast, plasma GH, melatonin, and norepinephrine concentrations did not increase. Plasma PRL, ACTH, and cortisol levels increased significantly after 20 mg CMI; again, there were no significant changes in plasma GH, melatonin, or norepinephrine concentrations. All subjects tolerated the 10-mg dose well, but the 20-mg dose caused nausea in three of six subjects. Desmethylclomipramine, a metabolite that inhibits reuptake of norepinephrine, was not detectable in plasma after either CMI dose. These results support the hypothesis that serotonin is involved in the regulation of PRL, cortisol, and ACTH in humans.
在正常受试者中研究了静脉注射氯米帕明(CMI,一种血清素再摄取抑制剂)的神经内分泌作用。在双盲、安慰剂对照条件下,分别给予10毫克和20毫克单剂量的CMI。10毫克CMI导致血浆催乳素(PRL)和皮质醇浓度显著升高;血浆促肾上腺皮质激素(ACTH)略有升高但不显著。相比之下,血浆生长激素(GH)、褪黑素和去甲肾上腺素浓度没有升高。20毫克CMI后,血浆PRL、ACTH和皮质醇水平显著升高;同样,血浆GH、褪黑素或去甲肾上腺素浓度没有显著变化。所有受试者对10毫克剂量耐受性良好,但20毫克剂量导致6名受试者中有3名出现恶心。在任一CMI剂量后,血浆中均未检测到去甲氯米帕明(一种抑制去甲肾上腺素再摄取的代谢产物)。这些结果支持了血清素参与人类PRL、皮质醇和ACTH调节的假说。