Schoups A, Dillen L, Claeys M, Duchateau A, Verbeuren T J, De Potter W P
Eur J Pharmacol. 1986 Jul 31;126(3):259-71. doi: 10.1016/0014-2999(86)90056-7.
The effects of single and long-term administration of the antidepressants imipramine, desimipramine, amitriptyline, zimelidine and maprotiline were studied in the rabbit brain. Special attention was given to the brain serotonin (5-HT) receptors. Our results show that in different areas of the rabbit brain, the binding sites for 5-HT display pharmacological characteristics very similar to those of the 5-HT1 and 5-HT2 receptors described for the rat brain. No significant correlation could be shown between the distribution of either of the receptors and the distribution of serotonergic nerve terminals (as measured by the 5-HT content and the [3H]5-HT accumulation). Addition of antidepressants to rabbit brain slices, in vitro, caused an inhibition of the [3H]5-HT accumulation. The compounds only weakly inhibited the binding of [3H]5-HT and [3H]ketanserin as compared to the inhibition caused by serotonergic agonists and antagonists. The [3H]5-HT accumulation in brain slices was markedly reduced 2 h after a single i.p. injection of imipramine. After a two-week administration of the antidepressants, the specific binding of neither [3H]5-HT nor [3H]ketanserin was significantly altered. The simultaneous determination of monoamine metabolites and of dopamine-beta-hydroxylase in the cerebrospinal fluid of these treated rabbits did not reveal any significant difference from the control animals.
在兔脑中研究了抗抑郁药丙咪嗪、去甲丙咪嗪、阿米替林、齐美利定和马普替林单次及长期给药的效果。特别关注了脑血清素(5-羟色胺,5-HT)受体。我们的结果表明,在兔脑的不同区域,5-HT的结合位点显示出与大鼠脑中描述的5-HT1和5-HT2受体非常相似的药理学特性。任一受体的分布与血清素能神经末梢的分布(通过5-HT含量和[3H]5-HT积累来测量)之间均未显示出显著相关性。在体外,向兔脑切片中添加抗抑郁药会导致[3H]5-HT积累受到抑制。与血清素能激动剂和拮抗剂所引起的抑制作用相比,这些化合物仅微弱地抑制了[3H]5-HT和[3H]酮舍林的结合。单次腹腔注射丙咪嗪2小时后,脑切片中的[3H]5-HT积累明显减少。在抗抑郁药给药两周后,[3H]5-HT和[3H]酮舍林的特异性结合均未发生显著改变。对这些接受治疗的兔子的脑脊液中的单胺代谢物和多巴胺-β-羟化酶进行同时测定,结果显示与对照动物相比没有任何显著差异。