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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Fluoxetine prevents stimulation-dependent fatigue of synaptic vesicle exocytosis in hippocampal neurons.
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Fluoxetine prevents stimulation-dependent fatigue of synaptic vesicle exocytosis in hippocampal neurons.

机译:氟西汀可预防海马神经元中突触小泡胞吐作用的刺激依赖性疲劳。

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摘要

Effects of the antidepressant fluoxetine on stimulation-dependent synaptic vesicle exocytosis were examined in cultured primary hippocampal neurons. Synaptic vesicles were fluorescently labeled in vitro with FM1-43, washed and subsequently destained in two consecutive cycles. Exocytosis was triggered by electric field stimulation and imaged by fluorescence microscopy. In control preparations, the second staining-destaining cycle caused a significant reduction of relative fluorescence loss, number of active synapses and half-decay time (t(50)). These fatigue effects were largely prevented by short-term administration of 1 microM fluoxetine, which was present before and during the second stimulation cycle. Fluoxetine concentrations above 10 microM inhibited exocytosis almost completely but showed no other toxic effects on neurons. Stressed neurons, grown under hyperosmotic conditions, were even more fatigue-protected by fluoxetine. These observations support the idea that therapeutic concentrations of fluoxetine enhance the recovery of neurotransmission from exhausting stimuli in healthy and in hyperosmotically stressed neurons as well.
机译:在培养的原代海马神经元中检查了抗抑郁药氟西汀对刺激依赖性突触小泡胞吐的影响。突触小泡在体外用FM1-43进行荧光标记,洗涤并随后在两个连续的循环中脱色。通过电场刺激触发胞吐作用,并通过荧光显微镜成像。在对照制剂中,第二次染色染色循环显着降低了相对荧光损失,活性突触数量和半衰期(t(50))。这些疲劳效应在很大程度上通过短期施用1 microM氟西汀(在第二个刺激周期之前和之中)而得到预防。氟西汀浓度超过10 microM时几乎完全抑制胞吐作用,但对神经元无其他毒性作用。在高渗条件下生长的应激神经元受到氟西汀的保护甚至更高。这些观察结果支持以下观点:治疗浓度的氟西汀可增强健康人和高渗压力神经元的疲劳刺激,从而恢复神经传递。

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