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Tonic 5nM DA Stabilizes Neuronal Output by Enabling Bidirectional Activity-Dependent Regulation of the Hyperpolarization Activated Current via PKA and Calcineurin

机译:Tonic 5nM DA通过启用经由PKA和钙调神经磷酸酶的超极化激活电流的双向活性依赖调节来稳定神经元输出

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摘要

Volume transmission results in phasic and tonic modulatory signals. The actions of tonic dopamine (DA) at type 1 DA receptors (D1Rs) are largely undefined. Here we show that tonic 5nM DA acts at D1Rs to stabilize neuronal output over minutes by enabling activity-dependent regulation of the hyperpolarization activated current (I h). In the presence but not absence of 5nM DA, I h maximal conductance (G max) was adjusted according to changes in slow wave activity in order to maintain spike timing. Our study on the lateral pyloric neuron (LP), which undergoes rhythmic oscillations in membrane potential with depolarized plateaus, demonstrated that incremental, bi-directional changes in plateau duration produced corresponding alterations in LP I hG max when preparations were superfused with saline containing 5nM DA. However, when preparations were superfused with saline alone there was no linear correlation between LP I hGmax and duty cycle. Thus, tonic nM DA modulated the capacity for activity to modulate LP I h G max; this exemplifies metamodulation (modulation of modulation). Pretreatment with the Ca2+-chelator, BAPTA, or the specific PKA inhibitor, PKI, prevented all changes in LP I h in 5nM DA. Calcineurin inhibitors blocked activity-dependent changes enabled by DA and revealed a PKA-mediated, activity-independent enhancement of LP I hG max. These data suggested that tonic 5nM DA produced two simultaneous, PKA-dependent effects: a direct increase in LP I h G max and a priming event that permitted calcineurin regulation of LP I h. The latter produced graded reductions in LP I hG max with increasing duty cycles. We also demonstrated that this metamodulation preserved the timing of LP’s first spike when network output was perturbed with bath-applied 4AP. In sum, 5nM DA permits slow wave activity to provide feedback that maintains spike timing, suggesting that one function of low-level, tonic modulation is to stabilize specific features of a dynamic output.
机译:体积传输会导致相位和音调调制信号。进补多巴胺(DA)对1型DA受体(D1Rs)的作用尚不清楚。在这里,我们显示,补剂5nM DA通过激活超极化激活电流(I h)的依赖于活性的调节作用,在D1R上稳定神经元的输出。在存在但不存在5nM DA的情况下,根据慢波活动的变化调整最大电导(I h),以维持峰值定时。我们对侧方幽门神经元(LP)进行研究,发现其膜电位与去极化高原发生有规律的振荡,当制剂与含有5nM DA的生理盐水进行超融合时,高原持续时间的增量双向变化会相应地改变LP I hG max。 。然而,当制剂仅与盐水融合时,LP I hGmax与占空比之间没有线性关系。因此,补品nM DA调节了调节LP I h G max的活性的能力。这举例说明了元调制(调制的调制)。用Ca2 +螯合剂BAPTA或特定的PKA抑制剂PKI进行预处理可以防止5nM DA中LP I h的所有变化。钙调神经磷酸酶抑制剂阻断了DA激活的活性依赖性变化,并揭示了PKA介导的LP I hG max的活性依赖性增强。这些数据表明,补品5nM DA可同时产生两种PKA依赖性作用:LP I h G max的直接增加和允许钙调神经磷酸酶调节LP I h的引发事件。后者随着占空比的增加逐步降低了LP I hG max 。我们还证明了当采用浴应用的4AP干扰网络输出时,这种元调制保留了LP首次尖峰的时序。总而言之,5nM DA允许慢波活动提供保持尖峰定时的反馈,这表明低电平调音的一种功能是稳定动态输出的特定功能。

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