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环核苷酸可诱导软体动物神经元中谷氨酸激活的氯离子电流产生长期增强。

Cyclic nucleotides induce long-term augmentation of glutamate-activated chloride current in molluscan neurons.

作者信息

Bukanova Julia V, Solntseva Elena I, Skrebitsky Vladimir G

机构信息

Brain Research Institute, Russian Academy of Medical Sciences, Per. Obukha 5, 105064, Moscow, Russia.

出版信息

Cell Mol Neurobiol. 2005 Dec;25(8):1185-94. doi: 10.1007/s10571-005-8371-7.

Abstract
  1. Literature data indicate that serotonin induces the long-term potentiation of glutamate (Glu) response in molluscan neurons. The aim of present work was to elucidate whether cyclic nucleotides can cause the same effect. 2. Experiments were carried out on isolated neurons of the edible snail (Helix pomatia) using a two-microelectrode voltage-clamp method. 3. In the majority of the cells examined, the application of Glu elicited a Cl- -current. The reversal potential (Er) of this current lied between -35 and -55 mV in different cells. 4. Picrotoxin, a blocker of Cl- -channels, suppressed this current equally on both sides of Er. Furosemide, an antagonist of both Cl- -channels and the Na+/K+/Cl- -cotransporter, had a dual effect on Glu-response: decrease in conductance, and shift of Er to negative potentials. 5. A short-term (2 min) cell treatment with 8-Br-cAMP or 8-Br-cGMP caused long-term (up to 30 min) change in Glu-response. At a holding potential of -60 mV, which was close to the resting level, an increase in Glu-activated inward current was observed. This potentiation seems to be related to the right shift of Er of Glu-activated Cl- -current rather than to the increase in conductance of Cl- -channels. The blocking effect of picrotoxin rested after 8-Br-cAMP treatment. 6. The change in the Cl- -homeostasis as a possible mechanism for the observed effect of cyclic nucleotides is discussed.
摘要
  1. 文献数据表明,血清素可诱导软体动物神经元中谷氨酸(Glu)反应的长期增强。本研究的目的是阐明环核苷酸是否能产生相同的效应。2. 使用双微电极电压钳法对可食用蜗牛(Helix pomatia)的分离神经元进行实验。3. 在大多数被检测的细胞中,施加Glu会引发Cl⁻电流。该电流的反转电位(Er)在不同细胞中介于 -35至 -55 mV之间。4. 氯通道阻滞剂匹鲁卡品在Er两侧同等程度地抑制该电流。呋塞米是氯通道和Na⁺/K⁺/Cl⁻共转运体的拮抗剂,对Glu反应有双重作用:电导降低,且Er向负电位偏移。5. 用8 - Br - cAMP或8 - Br - cGMP对细胞进行短期(2分钟)处理会导致Glu反应发生长期(长达30分钟)变化。在接近静息水平的 -60 mV的钳制电位下,观察到Glu激活的内向电流增加。这种增强似乎与Glu激活的Cl⁻电流的Er右移有关,而非与氯通道的电导增加有关。8 - Br - cAMP处理后匹鲁卡品的阻断作用消失。6. 讨论了Cl⁻稳态变化作为环核苷酸所观察到效应的一种可能机制。

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