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Electrophysiological Properties of Rostral Ventrolateral Medulla Presympathetic Neurons Modulated by the Respiratory Network in Rats

机译:呼吸网络对大鼠前额外侧前延髓髓质交感神经元的电生理特性

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摘要

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:呼吸模式发生器调节交感流出,低氧引起的挑战增强了交感流出。这种耦合是由于在延髓腹侧延髓(RVLM)中的呼吸调节前交感神经元引起的,但其下划线的电生理机制仍不清楚。为了更好地了解负责这种呼吸-交感神经耦合的神经基质,我们结合了正常大鼠和接受代谢挑战的原位制剂中RVLM交感神经元的免疫荧光,单细胞qRT-pCR和电生理学记录由慢性间歇性缺氧(CIH)产生。我们的研究结果表明,就内在电生理特性,呼吸突触输入和离子电流的表达而言,脊柱投射的钙胆碱能C1和非C1呼吸调节性RVLM交感神经元构成了异质神经元群体,尽管所有神经元均表现出持续的钠电流依赖性内在突触阻断后的起搏器特性。非C1呼吸调节的RVLM交感神经元的特定亚群在CIH后呈现出来自呼吸网络的增强的兴奋性突触输入。这种现象可能有助于在CIH大鼠中观察到的交感神经活动增强。我们得出的结论是,作为复杂神经元网络的一部分,不同的呼吸调节性RVLM交感神经交感神经元促成呼吸交感神经耦合的中央生成,响应CIH产生的挑战,呼吸交感神经活动引起呼吸相关的增加。

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