Ross S B, Kelder D
Acta Physiol Scand. 1977 Jan;99(1):27-36. doi: 10.1111/j.1748-1716.1977.tb10348.x.
The efflux of 3H-5-HT from a crude synaptosome preparation of the cerebral cortex of reserpinized rats was examined. The synaptosomes were loaded with 3H-5-HT by pre-incubation of the homogenate in presence of pargyline and desipramine in order to inhibit deamination of 5-HT and uptake into noradrenergic neurons. The synaptosomes were collected by centrifugation, washed and resuspended in 0.25 M sucrose. No spontaneous efflux of 5-HT was detectable at 0 degrees C but marked efflux was observed at 27 degrees C and 37 degrees C. 4-Chloroamphetamine, low external Na+ concentration, ouabain and the depolarizing agent veratridine markedly accelerated the initial (5 min) efflux. Inhibitors of the neuronal 5-HT uptake, e.g. chlorimipramine, H 102/09 and A 23189, antagonized the 5-HT efflux evoked by these means, whereas desipramine, which is a poor inhibitor of the 5-HT uptake, had only slight effect on the 5-HT efflux. It is suggested that 5-HT can be actively transported out from the synaptosomes by the reversed 5-HT uptake mechanism.
对利血平化大鼠大脑皮层粗制突触体制剂中3H-5-羟色胺(3H-5-HT)的流出进行了检测。通过在帕吉林和地昔帕明存在的情况下对匀浆进行预孵育,使突触体负载3H-5-HT,以抑制5-HT的脱氨基作用以及其被摄取到去甲肾上腺素能神经元中。通过离心收集突触体,洗涤后重悬于0.25M蔗糖中。在0℃时未检测到5-HT的自发流出,但在27℃和37℃时观察到明显的流出。4-氯苯丙胺、低细胞外钠离子浓度、哇巴因和去极化剂藜芦碱显著加速了最初(5分钟)的流出。神经元5-HT摄取抑制剂,如氯米帕明、H 102/09和A 23189,拮抗了这些方法所诱发的5-HT流出,而作为5-HT摄取较差抑制剂的地昔帕明,对5-HT流出仅有轻微影响。提示5-HT可通过反向5-HT摄取机制从突触体中被主动转运出去。