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多巴胺能调制前额皮质锥体神经元的轴突钾通道和动作电位波形。

Dopaminergic modulation of axonal potassium channels and action potential waveform in pyramidal neurons of prefrontal cortex.

机构信息

Institute of Neuroscience, State Key Laboratory of Neuroscience, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.

出版信息

J Physiol. 2013 Jul 1;591(13):3233-51. doi: 10.1113/jphysiol.2013.251058. Epub 2013 Apr 8.

Abstract

Voltage-gated K(+) (KV) channels play critical roles in shaping neuronal signals. KV channels distributed in the perisomatic regions and thick dendrites of cortical pyramidal neurons have been extensively studied. However, the properties and regulation of KV channels distributed in the thin axons remain unknown. In this study, by performing somatic and axonal patch-clamp recordings from layer 5 pyramidal neurons of prefrontal cortical slices, we showed that the rapidly inactivating A-currents mediated the transient K(+) currents evoked by action potential (AP) waveform command (KAP) at the soma, whereas the rapidly activating but slowly inactivating KV1-mediated D-currents dominated the KAP at the axon. In addition, activation of D1-like receptors for dopamine decreased the axonal K(+) currents, as a result of an increase in the activity of cAMP-PKA pathway. In contrast, activation of D2-like receptors showed an opposite effect on the axonal K(+) currents. Further experiments demonstrated that functional D1-like receptors were expressed at the main axon trunk and their activation could broaden the waveforms of axonal APs. Together, these results show that axonal KV channels were subjected to dopamine modulation, and this modulation could regulate the waveforms of propagating APs at the axon, suggesting an important role of dopaminergic modulation of axonal KV channels in regulating neuronal signalling.

摘要

电压门控钾离子 (KV) 通道在塑造神经元信号方面发挥着关键作用。分布在皮质锥体神经元的胞体区域和厚树突中的 KV 通道已得到广泛研究。然而,分布在细轴突中的 KV 通道的特性和调节仍不清楚。在这项研究中,通过对前额叶皮质切片第 5 层锥体神经元进行胞体和轴突膜片钳记录,我们表明,快速失活的 A 电流介导了动作电位 (AP) 波形命令 (KAP) 在胞体处诱发的瞬态 K(+)电流,而快速激活但缓慢失活的 KV1 介导的 D 电流则主宰了轴突处的 KAP。此外,多巴胺 D1 样受体的激活增加了 cAMP-PKA 途径的活性,从而减少了轴突中的 K(+)电流。相比之下,D2 样受体的激活对轴突 K(+)电流表现出相反的影响。进一步的实验表明,功能性 D1 样受体在主轴突干上表达,其激活可以拓宽轴突 AP 的波形。总之,这些结果表明,轴突 KV 通道受到多巴胺的调节,这种调节可以调节轴突上传播的 AP 的波形,提示多巴胺对轴突 KV 通道的调节在调节神经元信号传递中起着重要作用。

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