Sargent P A, Quested D J, Cowen P J
University Department of Psychiatry, Warneford Hospital, Oxford, UK.
Psychopharmacology (Berl). 1998 Nov;140(1):120-2. doi: 10.1007/s002130050747.
We measured the cortisol response to the 5-HT precursor, 5-hydroxytryptophan, (5-HTP) in seven patients with major depression before and after 8 weeks treatment with the tricyclic antidepressant, clomipramine. The cortisol response to 5-HTP was significantly increased following clomipramine treatment, suggesting that clomipramine, like selective serotonin re-uptake inhibitors (SSRIs), enhances this 5-HT2 receptor mediated response. Because other tricyclic antidepressants do not increase 5-HTP-mediated cortisol release, it seems unlikely that enhancement of 5-HT2 receptor function is a critical mechanism for antidepressant action. However, facilitation of neurotransmission at 5-HT2 receptors could account for the efficacy of clomipramine and SSRIs in the treatment of obsessive compulsive disorder and also for their liability to cause orgasmic dysfunction.
我们在7例重度抑郁症患者中,测量了在使用三环类抗抑郁药氯米帕明治疗8周前后,其对5-羟色胺前体5-羟色氨酸(5-HTP)的皮质醇反应。氯米帕明治疗后,对5-HTP的皮质醇反应显著增加,这表明氯米帕明与选择性5-羟色胺再摄取抑制剂(SSRI)一样,增强了这种5-HT2受体介导的反应。由于其他三环类抗抑郁药不会增加5-HTP介导的皮质醇释放,5-HT2受体功能增强似乎不太可能是抗抑郁作用的关键机制。然而,5-HT2受体处神经传递的促进作用可以解释氯米帕明和SSRI在治疗强迫症方面的疗效,也可以解释它们导致性高潮功能障碍的倾向。