Hall H, Sällemark M, Wedel I
Acta Pharmacol Toxicol (Copenh). 1984 May;54(5):379-84. doi: 10.1111/j.1600-0773.1984.tb01945.x.
Using in vitro receptor binding techniques, the effects of a number of different antidepressants on rat cerebral cortex receptors were investigated. In contrast to the tricyclic antidepressants, which potently inhibit several postsynaptic receptors, many atypical antidepressants have no or very little affinity for these receptors. Thus bupropion, amineptine, citalopram, fluoxetine, fluvoxamine and viloxazine are devoid of any activity, while amoxapine, doxepin and trazodone exert effects on a number of receptors. The implications of these receptor blocking effects are discussed.
运用体外受体结合技术,研究了多种不同抗抑郁药对大鼠大脑皮质受体的影响。与能有效抑制多种突触后受体的三环类抗抑郁药不同,许多非典型抗抑郁药对这些受体没有或只有极低的亲和力。因此,安非他酮、阿密曲替林、西酞普兰、氟西汀、氟伏沙明和维洛沙嗪没有任何活性,而阿莫沙平、多塞平和曲唑酮则对多种受体发挥作用。文中讨论了这些受体阻断作用的意义。