Lowy M T, Meltzer H Y
Department of Psychiatry, Case Western Reserve University, Cleveland, OH.
Biol Psychiatry. 1988 Apr 15;23(8):818-28. doi: 10.1016/0006-3223(88)90070-4.
The effects of MK-212 [6-chloro-2-(1-piperazinyl)-pyrazine] (10, 20, and 40 mg, orally), a centrally acting serotonin (5-HT) receptor agonist and placebo, on serum cortisol, prolactin, and growth hormone levels were studied in eight healthy men over 3-hr. MK-212 produced a dose-related increase in serum cortisol levels, with the 20- and 40-mg doses producing significant elevations. Serum prolactin levels were significantly elevated only by the 40-mg dose. Serum GH levels were not significantly modified by any dose of MK-212. The cortisol and prolactin responses to the 40-mg dose of MK-212 were positively correlated (rho = + 0.85, p less than 0.02). MK-212 was generally well tolerated by the subjects. Headache and nausea were observed at the higher doses, but did not appear to be related to the increase in serum cortisol and prolactin levels. MK-212 may stimulate the secretion of cortisol and prolactin in humans via a serotonin (5-HT2) receptor mechanism and may be a valuable tool with which to study 5-HT receptor sensitivity in humans.
研究了中枢作用性血清素(5-羟色胺,5-HT)受体激动剂MK-212[6-氯-2-(1-哌嗪基)-吡嗪](10、20和40毫克,口服)及安慰剂对8名健康男性3小时内血清皮质醇、催乳素和生长激素水平的影响。MK-212可使血清皮质醇水平呈剂量依赖性升高,20毫克和40毫克剂量可产生显著升高。仅40毫克剂量可使血清催乳素水平显著升高。任何剂量的MK-212均未显著改变血清生长激素水平。对40毫克剂量MK-212的皮质醇和催乳素反应呈正相关(rho = + 0.85,p < 0.02)。受试者对MK-212总体耐受性良好。在较高剂量时观察到头痛和恶心,但似乎与血清皮质醇和催乳素水平升高无关。MK-212可能通过血清素(5-HT2)受体机制刺激人体皮质醇和催乳素的分泌,可能是研究人体5-HT受体敏感性的一种有价值的工具。