Price L H, Charney D S, Heninger G R
Yale University School of Medicine, New Haven, CT.
Psychiatry Res. 1988 May;24(2):165-75. doi: 10.1016/0165-1781(88)90059-5.
Changes in serotonergic (5HT) neurotransmission may mediate the therapeutic actions of some antidepressant drugs. In the present study, the 5HT precursor L-tryptophan (L-TRP) was administered intravenously to nine depressed patients before and during treatment with the triazolopyridine antidepressant trazodone (TRZ). Neuroendocrine, subjective mood, and cardiovascular responses to L-TRP were assessed. Unlike tricyclic antidepressants and monoamine oxidase inhibitors, TRZ did not enhance the prolactin response to L-TRP and had little effect on other measures. Since other studies indicate that the TRP-induced increase of prolactin in humans may reflect 5HT function, the present study suggests that TRZ treatment does not enhance net 5HT function in depressed patients.
血清素能(5HT)神经传递的变化可能介导某些抗抑郁药物的治疗作用。在本研究中,对9名抑郁症患者在使用三唑吡啶类抗抑郁药曲唑酮(TRZ)治疗前及治疗期间静脉注射5HT前体L-色氨酸(L-TRP)。评估了对L-TRP的神经内分泌、主观情绪及心血管反应。与三环类抗抑郁药和单胺氧化酶抑制剂不同,TRZ并未增强对L-TRP的催乳素反应,且对其他指标影响甚微。由于其他研究表明,TRP诱导的人体催乳素升高可能反映5HT功能,本研究提示TRZ治疗不会增强抑郁症患者的净5HT功能。