Li M Y, Reith M E
Department of Biomedical and Therapeutic Sciences, College of Medicine, University of Illinois, Peoria 61656, USA.
Eur J Pharmacol. 1997 Dec 11;340(2-3):145-51. doi: 10.1016/s0014-2999(97)01421-0.
The involvement of K+ channels in the autoregulation of terminal serotonin (5-hydroxytryptamine, 5-HT) release was investigated by microdialysis in the hippocampus of conscious rats. Extracellular 5-HT was increased concentration-dependently by the K+ channel blocker quinine (10, 100 and 1000 microM in perfusate), and tetrodotoxin (10 microM) but not fluoxetine (5 microM) exerted a partially attenuating influence. The 5-HT1/2/6 receptor antagonist methiothepin (50 microM) increased dialysate 5-HT, most likely through 5-HT1B autoreceptors tonically activated in the hippocampus of awake rats as opposed to the previously reported lack of effect 5-HT1B autoreceptor blockade in anesthetized rats. The effect of methiothepin was greatly reduced by preperfusion with quinine (100 microM), consonant with a role for quinine-sensitive K+ channels in the autoregulation of 5-HT release in the hippocampus by 5-HT receptor antagonism. In contrast, the reduction in dialysate 5-HT induced by the 5-HT1 receptor agonist RU 24969 (1 microM), in the presence of fluoxetine (5 microM), persisted in the co-presence of quinine, consonant with the involvement of (extrasynaptic?) 5-HT autoreceptors not coupled with quinine-sensitive K+ channels.
通过微透析技术,在清醒大鼠的海马体中研究了钾离子通道在终末5-羟色胺(5-HT)释放的自动调节中的作用。钾离子通道阻滞剂奎宁(灌注液中浓度为10、100和1000微摩尔)可使细胞外5-HT浓度依赖性增加,河豚毒素(10微摩尔)也有部分减弱作用,但氟西汀(5微摩尔)无此作用。5-HT1/2/6受体拮抗剂美噻吨(50微摩尔)可增加透析液中5-HT,这很可能是通过在清醒大鼠海马体中持续激活的5-HT1B自身受体实现的,这与之前报道的在麻醉大鼠中5-HT1B自身受体阻断无作用相反。预先用奎宁(100微摩尔)灌注可大大降低美噻吨的作用,这与奎宁敏感的钾离子通道在5-HT受体拮抗作用对海马体中5-HT释放的自动调节中的作用一致。相反,在氟西汀(5微摩尔)存在的情况下,5-HT1受体激动剂RU 24969(1微摩尔)诱导的透析液中5-HT减少,在同时存在奎宁时仍然存在,这与(突触外?)5-HT自身受体的参与一致,这些自身受体与奎宁敏感的钾离子通道不偶联。