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从两个已确定的含5-羟色胺神经元释放内源性5-羟色胺以及5-羟色胺再摄取的生理作用。

Release of endogenous serotonin from two identified serotonin-containing neurones and the physiological role of serotonin re-uptake.

作者信息

Gerschenfeld H M, Hamon M, Paupardin-Tritsch D

出版信息

J Physiol. 1978 Jan;274:265-78. doi: 10.1113/jphysiol.1978.sp012146.

Abstract
  1. The amounts of endogenous serotonin (5-HT) released into the medium by the cerebro-buccal ganglionic ring of Aplysia californica incubated in artificial sea water (ASW) were measured. The rate of spontaneous 5-HT release varied between 0.4 and 1.2 p-mole per hour, which is less than 1% of the total 5-HT present in this preparation.2. Direct stimulation of the ordinarily silent 5-HT-containing giant cerebral neurones resulted in a 80-100% increase of the 5-HT released, but only when the 5-HT uptake was blocked by chlorimipramine (1-10 muM).3. High K(+) media (50 mM) also caused a significant increase in the amount of 5-HT released from the preparation provided that chlorimipramine (1-10 muM) was present in the incubation fluid.4. Co(2+) ions (10-30 mM) added to the incubating medium blocked the spontaneous leak of endogenous 5-HT as well as the release, in the presence of chlorimipramine, evoked either by stimulation of the 5-HT-giant cerebral neurones or high K(+)-media.5. In the presence of chlorimipramine or desmethylimipramine, the duration and/or the amplitude of the excitatory or the inhibitory synaptic potentials evoked in the buccal neurones by the stimulation of the 5-HT giant cerebral neurones were markedly enhanced.6. These results strongly support the idea that 5-HT is the synaptic transmitter released at the excitatory and inhibitory junctions established by the 5-HT giant cerebral neurones in the ipsilateral buccal ganglia. In addition, they underline the role of amine re-uptake in the physiological inactivation of 5-HT as a transmitter.
摘要
  1. 测定了在人工海水中孵育的加州海兔脑-口神经节环释放到培养基中的内源性5-羟色胺(5-HT)量。5-HT的自发释放速率在每小时0.4至1.2皮摩尔之间变化,这不到该制剂中总5-HT的1%。

  2. 直接刺激通常沉默的含5-HT的巨大脑神经元会导致5-HT释放增加80%-100%,但仅当5-HT摄取被氯米帕明(1-10μM)阻断时才会如此。

  3. 高钾培养基(50 mM)也会导致制剂释放的5-HT量显著增加,前提是孵育液中存在氯米帕明(1-10μM)。

  4. 添加到孵育培养基中的钴离子(10-30 mM)阻断了内源性5-HT的自发泄漏以及在氯米帕明存在下由刺激5-HT巨大脑神经元或高钾培养基引起的释放。

  5. 在氯米帕明或去甲氯米帕明存在的情况下,刺激5-HT巨大脑神经元在口神经元中诱发的兴奋性或抑制性突触电位的持续时间和/或幅度会显著增强。

  6. 这些结果有力地支持了5-HT是由5-HT巨大脑神经元在同侧口神经节建立的兴奋性和抑制性连接处释放的突触递质这一观点。此外,它们强调了胺再摄取在5-HT作为递质的生理失活中的作用。

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