Menkes D B, Aghajanian G K, Gallager D W
Eur J Pharmacol. 1983 Jan 28;87(1):35-41. doi: 10.1016/0014-2999(83)90047-x.
Binding of [3H]prazosin, a selective alpha 1-adrenoceptor antagonist, to thalamic membranes was studied following chronic treatment of rats with tricyclic antidepressants. Rosenthal analysis showed no change in the number or affinity of antagonist binding sites; however, the ability of the alpha 1-agonist phenylephrine to compete for these sites was significantly enhanced after chronic tricyclic treatment. This result is consistent with previous studies showing physiological alpha 1-supersensitivity in thalamus after chronic antidepressant administration.
在用三环类抗抑郁药长期治疗大鼠后,研究了选择性α1-肾上腺素能受体拮抗剂[3H]哌唑嗪与丘脑膜的结合情况。罗森塔尔分析表明拮抗剂结合位点的数量或亲和力没有变化;然而,在三环类药物长期治疗后,α1-激动剂去氧肾上腺素竞争这些位点的能力显著增强。这一结果与先前的研究一致,即在长期给予抗抑郁药后丘脑出现生理性α1-超敏反应。