Tokarski Krzysztof, Zahorodna Agnieszka, Bobula Bartosz, Hess Grzegorz
Department of Physiology, Institute of Pharmacology, Polish Academy of Sciences, Smetna 12, 31-343, Krakow, Poland.
Brain Res. 2003 Dec 12;993(1-2):230-4. doi: 10.1016/j.brainres.2003.09.015.
In the CA1 area of rat hippocampal slices, a combined application of 5-CT, a potent 5-HT(1A) and 5-HT(7) receptor agonist, and WAY 100635, a selective 5-HT(1A) receptor antagonist, resulted in a reversible increase of the CA1 extracellular population spike amplitude. In whole-cell recording from identified pyramidal neurons, the effects of 5-CT applied in the presence of WAY 100635 involved a reduction of the slow afterhyperpolarization (sAHP) and the frequency adaptation of action potential firing, which could be blocked by a specific 5-HT(7) receptor antagonist SB 269970. The results indicate that the activation of 5-HT(7) receptors increases the excitability of hippocampal CA1 pyramidal cells.
在大鼠海马切片的CA1区,强效5-羟色胺(5-HT)(1A)和5-HT(7)受体激动剂5-羧色胺(5-CT)与选择性5-HT(1A)受体拮抗剂WAY 100635联合应用,导致CA1细胞外群体峰电位幅度可逆性增加。在对已识别的锥体神经元进行全细胞记录时,在WAY 100635存在的情况下应用5-CT的效应包括慢后超极化(sAHP)的降低和动作电位发放的频率适应性,这可被特异性5-HT(7)受体拮抗剂SB 269970阻断。结果表明,5-HT(7)受体的激活增加了海马CA1锥体细胞的兴奋性。