Nathan P J, Norman T R, Burrows G D
Department of Psychiatry, University of Melbourne, Australia.
J Pineal Res. 1996 Sep;21(2):55-8. doi: 10.1111/j.1600-079x.1996.tb00271.x.
The effect on nocturnal melatonin secretion of acute administration of the indirectly acting serotonin (5-HT) receptor agonists d-fenfluramine (30 mg) and paroxetine (20 mg) and a partial 5-HT1A receptor agonist ipsapirone (20 mg) was investigated in healthy male volunteers and compared to a placebo condition. Each subject (n = 8) received each drug on one occasion over a 4 week study period, with drug administration separated by 1 week. A randomized, counter-balanced design was used. Drugs or placebo were administered at 2,000 hours in the light, and all blood samples were collected throughout the night in the dark at regular intervals until 0600 hours. Neither d-fenfluramine, paroxetine, or ipsapirone following acute dosage had a statistically significant effect on nocturnal melatonin synthesis. The lack of effect seen with d-fenfluramine, paroxetine, and ipsapirone may be due to limitations imposed by the dose requirements.
在健康男性志愿者中研究了间接作用的血清素(5-羟色胺,5-HT)受体激动剂右旋芬氟拉明(30毫克)、帕罗西汀(20毫克)和部分5-HT1A受体激动剂伊沙匹隆(20毫克)急性给药对夜间褪黑素分泌的影响,并与安慰剂条件进行比较。在为期4周的研究期间,每个受试者(n = 8)在一个时间段接受每种药物,药物给药间隔为1周。采用随机、平衡设计。药物或安慰剂在光照下的20:00给药,所有血样在黑暗中于夜间定期采集,直至06:00。急性给药后,右旋芬氟拉明、帕罗西汀或伊沙匹隆对夜间褪黑素合成均无统计学显著影响。右旋芬氟拉明、帕罗西汀和伊沙匹隆未见效果可能是由于剂量要求所限。