Zhang L
Department of Anaesthesia Research, McGill University, Montréal, Qué., Canada.
Can J Physiol Pharmacol. 1991 Feb;69(2):154-63. doi: 10.1139/y91-022.
The effects of 5-hydroxytryptamine (5-HT) on spinal motoneurons were examined in pentobarbital-anaesthetized cats and in nonanaesthetized decerebrate cats by intracellular recording and extracellular iontophoresis of 5-HT. 5-HT first induced a depolarization and then a long-lasting hyperpolarization (up to 60 min) with unchanged input resistance. The slow hyperpolarization was prevented by the 5-HT antagonists ketanserin (5-HT2), methysergide, and spiperone (5-HT1,2) and mimicked by the agonist (+/-)-1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane (5-HT2). The post-spike after hyperpolarization was enhanced after application of 5-HT. A depolarization was induce by the 5-HT agonists (+/-)-8-hydroxy-(2)-(di-n-propylamino)tetralin (5-HT1A) and 1-(2-methoxyphenyl)piperazine (5-HT1). Possible mechanisms for the 5-HT-induced hyperpolarization and its intracellular medication are discussed. The present data suggest multiple effects of 5-HT on cat spinal motoneurons.
通过细胞内记录以及5-羟色胺(5-HT)的细胞外离子电泳法,在戊巴比妥麻醉的猫和未麻醉的去大脑猫身上研究了5-羟色胺(5-HT)对脊髓运动神经元的影响。5-HT首先诱导去极化,然后是持续较长时间的超极化(长达60分钟),同时输入电阻不变。5-HT拮抗剂酮色林(5-HT2)、麦角酰二乙胺和螺哌隆(5-HT1,2)可阻止这种缓慢的超极化,而激动剂(±)-1-(2,5-二甲氧基-4-碘苯基)-2-氨基丙烷(5-HT2)可模拟这种超极化。应用5-HT后,峰后超极化增强。5-HT激动剂(±)-8-羟基-(2)-(二正丙基氨基)四氢萘(5-HT1A)和1-(2-甲氧基苯基)哌嗪(5-HT1)可诱导去极化。本文讨论了5-HT诱导超极化及其细胞内作用的可能机制。目前的数据表明5-HT对猫脊髓运动神经元有多种作用。