首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Electrophysiological properties of rostral ventrolateral medulla presympathetic neurons modulated by the respiratory network in rats
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Electrophysiological properties of rostral ventrolateral medulla presympathetic neurons modulated by the respiratory network in rats

机译:呼吸道腹膜外髓对联神经元对大鼠呼吸网络调节的电生理性质

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The respiratory pattern generator modulates the sympathetic outflow, the strength of which is enhanced by challenges produced by hypoxia. This coupling is due to the respiratory-modulated presympathetic neurons in the rostral ventrolateral medulla (RVLM), but the underlining electrophysiological mechanisms remain unclear. For a better understanding of the neural substrates responsible for generation of this respiratory-sympathetic coupling, we combined immunofluorescence, single cell qRT-pCR, and electrophysiological recordings of the RVLM presympathetic neurons in in situ preparations from normal rats and rats submitted to a metabolic challenge produced by chronic intermittent hypoxia (CIH). Our results show that the spinally projected cathecholaminergic C1 and non-C1 respiratory-modulated RVLM presympathetic neurons constitute a heterogeneous neuronal population regarding the intrinsic electrophysiological properties, respiratory synaptic inputs, and expression of ionic currents, albeit all neurons presented persistent sodium current-dependent intrinsic pacemaker properties after synaptic blockade. A specific subpopulation of non-C1 respiratory-modulated RVLM presympathetic neurons presented enhanced excitatory synaptic inputs from the respiratory network after CIH. This phenomenon may contribute to the increased sympathetic activity observed in CIH rats. We conclude that the different respiratory-modulated RVLM presympathetic neurons contribute to the central generation of respiratory-sympathetic coupling as part of a complex neuronal network, which in response to the challenges produced by CIH contribute to respiratory-related increase in the sympathetic activity.
机译:呼吸器图案发生器调节交感神经流出,其强度通过缺氧产生的挑战增强。该偶联是由于呼吸器口腔外侧髓质(RVLM)中的呼吸调制的假手术神经元,但下划线的电生理机制仍然不清楚。为了更好地了解负责这种呼吸道同情偶联的神经底物,我们组合免疫荧光,单细胞QRT-PCR和RVLM PursyMpathetic神经元的电生理记录,原位制剂来自正常大鼠和大鼠提交给代谢挑战的大鼠由慢性间歇性缺氧(CIH)产生。我们的研究结果表明,脊髓突出的CatheCholaminergic C1和非C1呼吸调制的RVLM假设神经元构成了关于内在电生理学性质,呼吸突触输入和离子电流表达的异质神经元群,尽管所有神经元呈现持久性钠电流依赖性内在内部突触后的起搏器属性。非C1呼吸调制RVLM假设神经元的特定亚群呈现CIH后呼吸网络的增强兴奋性突触输入。这种现象可能有助于CIH大鼠中观察到的同情活性增加。我们得出结论,不同呼吸调制的RVLM假设神经元有助于作为复杂神经元网络的一部分的呼吸道交感神经耦合的呼吸道 - 交感偶联的一部分,这是响应CIH产生的呼吸相关的呼吸相关的挑战。

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