Harel-Dupas C, Cloëz I, Fillion G
Unité de Pharmacologie Neuro-Immuno-Endocrinienne de l'Institut Pasteur, Paris, France.
Eur Neuropsychopharmacol. 1991 May;1(2):157-64. doi: 10.1016/0924-977x(91)90717-9.
The effects of antidepressant drugs on the m-trifluoromethylphenylpiperazine (TFMPP)-induced inhibition of K(+)-evoked [3H]acetylcholine (3H-ACh) release were studied in rat or guinea-pig hippocampal synaptosomes. The serotonergic agonist TFMPP dose-dependently inhibited the K(+)-evoked release of 3H-ACh in rat hippocampus (IC50 = 53 microM). Chlorimipramine (5-500 nM), a typical tricyclic antidepressant, and minaprine (1-100 nM), an atypical antidepressant drug, partially antagonized the effect of TFMPP on 3H-ACh release in a dose-dependent manner. Other antidepressants (imipramine, citalopram, indalpine, fluoxetine, fluvoxamine, oxaprotiline, mianserine, nomifensine), at concentrations ranging from 10 to 500 nM, produced similar effects. Drugs with no antidepressant effect, such as chlorpromazine, clobazam, and cocaine (50, 100 and 500 nM), were without significant influence on the TFMPP effect. In guinea-pig hippocampal synaptosomes, minaprine (50 nM) also reduced the TFMPP-induced inhibition of 3H-ACh release, whilst clobazam (50 nM) was inactive. These results suggest that antidepressant drugs interact in vitro with heterologous serotonergic presynaptic receptors on cholinergic nerve terminals in rat and guinea-pig hippocampus.
在大鼠或豚鼠海马突触体中研究了抗抑郁药对间三氟甲基苯基哌嗪(TFMPP)诱导的钾离子激发的[3H]乙酰胆碱(3H-ACh)释放抑制作用的影响。5-羟色胺能激动剂TFMPP剂量依赖性地抑制大鼠海马中钾离子激发的3H-ACh释放(IC50 = 53微摩尔)。典型的三环抗抑郁药氯米帕明(5-500纳摩尔)和非典型抗抑郁药米那普明(1-100纳摩尔)以剂量依赖性方式部分拮抗TFMPP对3H-ACh释放的作用。其他抗抑郁药(丙咪嗪、西酞普兰、因达品、氟西汀、氟伏沙明、奥沙普替林、米安色林、诺米芬辛)在10至500纳摩尔浓度范围内产生类似作用。无抗抑郁作用的药物,如氯丙嗪、氯巴占和可卡因(50、100和500纳摩尔)对TFMPP的作用无显著影响。在豚鼠海马突触体中,米那普明(50纳摩尔)也减少了TFMPP诱导的3H-ACh释放抑制作用,而氯巴占(50纳摩尔)则无活性。这些结果表明,抗抑郁药在体外与大鼠和豚鼠海马胆碱能神经末梢上的异源性5-羟色胺能突触前受体相互作用。