Doggrell S A, Vincent L
J Pharm Pharmacol. 1981 Nov;33(11):720-4. doi: 10.1111/j.2042-7158.1981.tb13912.x.
The effects of antidepressants of tricyclic (amitriptyline, nortriptyline, protriptyline, doxepin, imipramine, and desipramine) and atypical (maprotiline, nomifensine, tandamine, viloxazine, CGP 6085A, and YM-08054-1) structures on contractile responses to exogenously applied acetylcholine and (-) noradrenaline were studied in rat isolated anococcygeus muscle previously incubated with 6-hydroxydopamine. Atropine, amitriptyline, protriptyline, doxepin, imipramine, maprotiline and nortriptyline inhibited contractile responses to acetylcholine whereas desipramine, nomifensine, tandamine, viloxazine, CGP 6085A and YM 08054-1 did not. The contractile responses to (-)-noradrenaline were inhibited by low concentrations of tricyclic antidepressants and by higher concentrations of the atypical agents. These results illustrate that, in the preparation, the order of potency of antidepressants as muscarinic and as postsynaptic alpha-adrenoceptor antagonists is similar. The ability of tricyclic, but not atypical agents, to increase the concentration of noradrenaline bound to postsynaptic alpha-adrenoceptors may be severely limited by the antagonistic effect these agents have at this receptor.
在预先用6-羟基多巴胺孵育的大鼠离体肛门尾骨肌中,研究了三环类(阿米替林、去甲替林、普罗替林、多塞平、丙咪嗪和地昔帕明)和非典型结构(马普替林、诺米芬辛、坦达明、维洛沙嗪、CGP 6085A和YM-08054-1)抗抑郁药对外源性应用乙酰胆碱和(-)去甲肾上腺素收缩反应的影响。阿托品、阿米替林、普罗替林、多塞平、丙咪嗪、马普替林和去甲替林抑制了对乙酰胆碱的收缩反应,而地昔帕明、诺米芬辛、坦达明、维洛沙嗪、CGP 6085A和YM 08054-1则没有。低浓度的三环类抗抑郁药和高浓度的非典型药物抑制了对(-)-去甲肾上腺素的收缩反应。这些结果表明,在该制剂中,抗抑郁药作为毒蕈碱和突触后α-肾上腺素能受体拮抗剂的效价顺序相似。三环类药物而非非典型药物增加与突触后α-肾上腺素能受体结合的去甲肾上腺素浓度的能力可能会受到这些药物在该受体上的拮抗作用的严重限制。