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首页> 外文期刊>Journal of Neurophysiology >Multiple effects of dopamine on layer V pyramidal cell excitability in rat prefrontal cortex.
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Multiple effects of dopamine on layer V pyramidal cell excitability in rat prefrontal cortex.

机译:多巴胺对大鼠前额叶皮层V层锥体细胞兴奋性的多重影响。

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摘要

The mechanisms underlying the inhibitory effects of dopamine (DA) on layer V pyramidal neuron excitability in the prelimbic region of the rat medial prefrontal cortex were investigated. Under control conditions, DA depressed both action potential generation (driven by somatic current injection) and input resistance (R(N)). The presence of GABA(A) receptor antagonists blocked DA-induced depression of action potential generation and revealed a delayed increase in excitability that persisted for the duration of experimental recording, up to 20 min following the washout of DA. In contrast to spike generation, disinhibition did not affect the transient depression of R(N) produced by DA, suggesting independent actions of DA on spike generation and R(N). Consistent with the hypothesis that DA acts to decrease pyramidal cell output via a GABAergic mechanism, DA increased the frequency of spontaneous inhibitory postsynaptic currents in both the absence and presence of TTX. Furthermore focal application of GABA to a perisomatic region mimicked the inhibitory effect of DA on spike production without affecting R(N). Focal application of bicuculline to the same location reversed the inhibitory effect of bath-applied DA on spike generation, while again having no effect on R(N). The depression of R(N) by DA was both occluded and mimicked by the Na(+) channel blocker TTX, suggesting the involvement of a Na(+) conductance in reducing pyramidal cell R(N) during the acute presence of DA. Together these data demonstrate that the acute presence of DA decreases pyramidal neuron excitability by two independent mechanisms. At the same time DA triggers a delayed and longer-lasting increase in excitability that is partially masked by synaptic inhibition.
机译:研究了多巴胺(DA)抑制大鼠内侧前额叶皮层前缘区V层锥体神经元兴奋性的潜在机制。在控制条件下,DA抑制了动作电位的产生(由体电流注入驱动)和输入电阻(R(N))。 GABA(A)受体拮抗剂的存在阻止了DA诱导的动作电位产生的降低,并揭示了兴奋性的延迟增加,这种兴奋性持续存在于实验记录的过程中,直至DA洗脱后20分钟。与峰值产生相反,去抑制作用不影响DA产生的R(N)的瞬时抑制,表明DA对峰值产生和R(N)的独立作用。与DA通过GABA能机制减少锥体细胞输出的假设相一致,DA在缺乏和存在TTX的情况下增加了自发抑制突触后电流的频率。此外,将GABA集中应用到周边区域模仿了DA对穗产生的抑制作用,而不影响R(N)。在同一位置局部施用小花碱逆转了浴涂DA对加标生成的抑制作用,而再次对R(N)没有影响。 Na(+)通道阻滞剂TTX阻断并模仿了DA对R(N)的抑制作用,这表明在DA急性存在期间,Na(+)电导参与了锥体细胞R(N)的还原。这些数据一起证明DA的急性存在通过两种独立的机制降低了锥体神经元的兴奋性。同时,DA会引起兴奋性的延迟和持续时间延长,而这种兴奋作用会被突触抑制部分掩盖。

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