膈神经中NaV1.6抑制与呼吸衰竭的关系。

Rebecca M Klein, Mark E Layton, Hillary Regan, Christopher P Regan, Yuxing Li, Tracey Filzen, Matt Cato, Michelle K Clements, Jixin Wang, Raul Sanoja, Thomas J Greshock, Anthony J Roecker, Joseph E Pero, Ron Kim, Christopher Burgey, Christopher T John, Ying-Hong Wang, Neetesh Bhandari, Arie Struyk, Richard L Kraus, Darrell A Henze, Andrea K Houghton
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引用次数: 0

摘要

作为鉴定治疗疼痛的NaV1.7有效抑制剂的药物发现工作的一部分,我们观察到抑制剂在体内产生意想不到的心血管和呼吸作用。具体来说,给啮齿动物施用抑制剂会产生心血管参数和呼吸停止的变化。我们试图通过体外和离体实验研究化合物对NaV1.5、NaV1.4和NaV1.6的选择性来确定体内不良反应的机制。与NaV1.6相比,缺乏足够NaV1.7选择性的抑制剂与啮齿动物体内给药后的呼吸停止有关。对大鼠呼吸频率的影响与离体半切大鼠膈肌模型和体外NaV1.6效价的影响一致。此外,在已知会导致大鼠呼吸停止的暴露中观察到膈神经信号的直接阻断。总之,这些结果支持NaV1.6在膈神经信号传导和呼吸功能中的重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Association of respiratory failure with inhibition of NaV1.6 in the phrenic nerve.

Association of respiratory failure with inhibition of NaV1.6 in the phrenic nerve.

Association of respiratory failure with inhibition of NaV1.6 in the phrenic nerve.

Association of respiratory failure with inhibition of NaV1.6 in the phrenic nerve.

As part of a drug discovery effort to identify potent inhibitors of NaV1.7 for the treatment of pain, we observed that inhibitors produced unexpected cardiovascular and respiratory effects in vivo. Specifically, inhibitors administered to rodents produced changes in cardiovascular parameters and respiratory cessation. We sought to determine the mechanism of the in vivo adverse effects by studying the selectivity of the compounds on NaV1.5, NaV1.4, and NaV1.6 in in vitro and ex vivo assays. Inhibitors lacking sufficient NaV1.7 selectivity over NaV1.6 were associated with respiratory cessation after in vivo administration to rodents. Effects on respiratory rate in rats were consistent with effects in an ex vivo hemisected rat diaphragm model and in vitro NaV1.6 potency. Furthermore, direct blockade of the phrenic nerve signaling was observed at exposures known to cause respiratory cessation in rats. Collectively, these results support a significant role for NaV1.6 in phrenic nerve signaling and respiratory function.

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