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氯离子通道-1 抑制作为加速大鼠神经肌肉阻滞后骨骼肌恢复的机制。

ClC-1 Inhibition as a Mechanism for Accelerating Skeletal Muscle Recovery After Neuromuscular Block in Rats.

机构信息

NMD Pharma, Aarhus, Denmark.

Department of Public Health, Aarhus University, Aarhus, Denmark.

出版信息

Nat Commun. 2024 Oct 28;15(1):9289. doi: 10.1038/s41467-024-53237-x.

Abstract

Neuromuscular blocking agents are used commonly to induce skeletal muscle relaxation during surgery. While muscle relaxation facilitates surgical procedures and tracheal intubation, adequate recovery of muscle function after surgery is required to support pulmonary function, and even mild residual neuromuscular block increases the risk of severe postoperative pulmonary complications. While recovery of muscle function after surgery involving neuromuscular blocking agents can be monitored and, in addition, be accelerated by use of current antagonists (reversal agents), there is a clear clinical need for a safe drug to antagonize all types of neuromuscular blocking agents. Here, we show that inhibition of the skeletal muscle-specific chloride ion (Cl) channel, the ClC-1 channel, markedly accelerates recovery of both single contraction (twitch) and, important physiologically, sustained (tetanic) contractions in a rat model mimicking neuromuscular blocking agent-induced muscle block used during surgery. This suggests ClC-1 inhibition as a mechanism for fast and efficacious recovery of neuromuscular function induced by any neuromuscular blocking agents.

摘要

神经肌肉阻滞剂常用于手术中诱导骨骼肌松弛。虽然肌肉松弛有助于手术操作和气管插管,但手术后需要足够的肌肉功能恢复以支持肺功能,即使是轻度的残余神经肌肉阻滞也会增加严重术后肺部并发症的风险。虽然可以监测和加速使用当前拮抗剂(逆转剂)来监测手术后使用神经肌肉阻滞剂的肌肉功能恢复,但显然需要一种安全的药物来拮抗所有类型的神经肌肉阻滞剂。在这里,我们表明抑制骨骼肌特异性氯离子(Cl)通道,即 ClC-1 通道,可显著加速模拟手术中使用的神经肌肉阻滞剂诱导的肌肉阻滞的大鼠模型中单次收缩(抽搐)和重要的生理收缩(强直)的恢复。这表明 ClC-1 抑制作为任何神经肌肉阻滞剂诱导的神经肌肉功能快速有效恢复的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/586f/11519510/9a2335d43e9c/41467_2024_53237_Fig1_HTML.jpg

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