Tokarski Krzysztof, Zahorodna Agnieszka, Bobula Bartosz, Grzegorzewska Malgorzata, Pitra Patrycja, Hess Grzegorz
Institute of Pharmacology, Polish Academy of Sciences, Kraków.
Eur J Pharmacol. 2005 Nov 7;524(1-3):60-6. doi: 10.1016/j.ejphar.2005.09.014. Epub 2005 Oct 25.
The effects of a selective serotonin reuptake inhibitor, citalopram, and a tricyclic antidepressant drug, imipramine, administered repetitively for 14 days, were investigated ex vivo in rat hippocampal slices. Spontaneous epileptiform bursts were recorded from the CA3 area in nominally Mg(2+)-free incubation conditions. 5-carboxamidotryptamine (5-CT) dose-dependently increased bursting frequency in the presence of N-[2-[4-(2-methoxyphenyl)-1 piperazinyl]ethyl]-N-2-pyridinylcyclohexanecarboxamide (WAY 100635). This effect could be dose-dependently blocked by (2R)-1-[(3-Hydroxyphenyl)sulfonyl]-2-[2-(4-methyl-1-piperidinyl)ethyl]pyrrolidine hydrochloride (SB 269970), thus implicating the involvement of 5-HT(7) receptors. Repeated treatment with citalopram or imipramine resulted in an attenuation of the excitatory effects of the activation of hippocampal 5-HT(7) receptor.
在大鼠海马切片上进行离体研究,考察了选择性5-羟色胺再摄取抑制剂西酞普兰和三环类抗抑郁药丙咪嗪连续给药14天的效果。在无镁的孵育条件下,记录CA3区的自发性癫痫样脉冲。在N-[2-[4-(2-甲氧基苯基)-1-哌嗪基]乙基]-N-2-吡啶基环己烷甲酰胺(WAY 100635)存在的情况下,5-羧基胺色胺(5-CT)剂量依赖性地增加脉冲频率。该效应可被盐酸(2R)-1-[(3-羟基苯基)磺酰基]-2-[2-(4-甲基-1-哌啶基)乙基]吡咯烷(SB 269970)剂量依赖性地阻断,从而提示5-HT(7)受体参与其中。西酞普兰或丙咪嗪重复给药导致海马5-HT(7)受体激活所产生的兴奋效应减弱。