Sharpley A L, Gregory C A, Solomon R A, Cowen P J
MRC Unit of Clinical Pharmacology, Littlemore Hospital, Oxford, U.K.
J Affect Disord. 1990 Aug;19(4):273-7. doi: 10.1016/0165-0327(90)90105-h.
The 5-HT2 receptor antagonist cyproheptadine significantly increased slow wave sleep in 12 healthy control subjects but not in 12 patients with a history of major depression, maintained on tricyclic antidepressant treatment. Cyproheptadine produced a similar reduction in REM sleep in both groups of subjects. The results are consistent with the hypothesis that tricyclic antidepressant treatment alters brain 5-HT2 receptor sensitivity, but a primary abnormality in slow wave sleep regulation in depressed patients cannot be excluded.
5-羟色胺2(5-HT2)受体拮抗剂赛庚啶可显著增加12名健康对照者的慢波睡眠,但对12名正在接受三环类抗抑郁药治疗且有重度抑郁病史的患者却无此作用。赛庚啶使两组受试者的快速眼动睡眠均有相似程度的减少。这些结果与三环类抗抑郁药治疗会改变大脑5-HT2受体敏感性这一假说相符,但不能排除抑郁症患者慢波睡眠调节存在原发性异常的可能性。