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

Author

Listed:
  • Marianne Skals

    (NMD Pharma)

  • Martin Broch-Lips

    (NMD Pharma)

  • Martin Brandhøj Skov

    (NMD Pharma)

  • Anders Riisager

    (NMD Pharma)

  • Judith Ceelen

    (NMD Pharma)

  • Ole Bækgaard Nielsen

    (Aarhus University)

  • Sorin J. Brull

    (Mayo Clinic College of Medicine and Science)

  • Hans D. Boer

    (Martini General Hospital Groningen)

  • Thomas Holm Pedersen

    (NMD Pharma
    Aarhus University)

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.

Suggested Citation

  • Marianne Skals & Martin Broch-Lips & Martin Brandhøj Skov & Anders Riisager & Judith Ceelen & Ole Bækgaard Nielsen & Sorin J. Brull & Hans D. Boer & Thomas Holm Pedersen, 2024. "ClC-1 Inhibition as a Mechanism for Accelerating Skeletal Muscle Recovery After Neuromuscular Block in Rats," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-53237-x
    DOI: 10.1038/s41467-024-53237-x
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