Taylor D P, Carter R B, Eison A S, Mullins U L, Smith H L, Torrente J R, Wright R N, Yocca F D
Department of Neuropharmacology, Bristol-Myers Squibb Company, Wallingford, CT 06492-7600, USA.
J Clin Psychiatry. 1995;56 Suppl 6:3-11.
Nefazodone is a new antidepressant drug with a pharmacologic profile distinct from that of the tricyclic, monoamine oxidase inhibitor, and serotonin selective reuptake inhibitor antidepressants. Nefazodone was initially discovered for its ability to block 5-HT2A receptors and its reduced potency as an alpha 1-adrenergic blocker. It was later shown to inhibit both serotonin and norepinephrine uptake in vitro, attributes which most likely impart its clinical efficacy and which differentiate nefazodone from its chemical predecessor trazodone. The combination of these two mechanisms may ultimately result in a facilitation of 5-HT1A-mediated neurotransmission, which may be beneficial for treating symptoms of depression as evidenced by recent clinical findings. In addition, the preclinical profile of nefazodone demonstrates that it has decreased anticholinergic and antihistaminic activity relative to traditional agents. Clinical findings to date are consistent with these observations.
奈法唑酮是一种新型抗抑郁药,其药理学特性与三环类、单胺氧化酶抑制剂及5-羟色胺选择性再摄取抑制剂类抗抑郁药不同。奈法唑酮最初因其能阻断5-HT2A受体及作为α1-肾上腺素能阻滞剂活性较低而被发现。后来发现它在体外能抑制5-羟色胺和去甲肾上腺素的摄取,这些特性很可能是其临床疗效的基础,也是奈法唑酮与其化学前身曲唑酮的区别所在。这两种机制的结合最终可能会促进5-HT1A介导的神经传递,最近的临床研究结果表明,这可能对治疗抑郁症症状有益。此外,奈法唑酮的临床前研究表明,与传统药物相比,它的抗胆碱能和抗组胺活性有所降低。目前的临床研究结果与这些观察结果一致。