Local anesthetic 'in-situ' toxicity during peripheral nerve blocks: update on mechanisms and prevention

Karine Nouette-Gaulain1, Xavier Capdevila, Rodrigue Rossignol

  • 1University Bordeaux, Maladies Rares, Génétique et Métabolique, Bordeaux, France. karine.nouette-gaulain@chu-bordeaux.fr

Abstract

Insights

Local anesthetics used in nerve blocks can cause cell toxicity in neurons and myocytes. Understanding these effects and optimizing protocols may prevent severe lesions and improve patient safety.

Area of Science:

  • Cell biology
  • Toxicology
  • Anesthesiology

Background:

  • Peripheral nerve blocks are common procedures.
  • Local anesthetics can cause undesired side effects due to toxicity on neurons and myocytes.
  • The cell targets and mechanisms of local anesthetic toxicity are increasingly understood.

Purpose of the Study:

  • To review the known effects of local anesthetics on neuronal and myocyte targets.
  • To summarize the pathways involved in local anesthetic-induced cell toxicity.
  • To discuss clinical implications and potential preventive strategies.

Main Methods:

  • Review of existing literature on local anesthetic toxicity.
  • Analysis of phenotypic, biochemical, and cell biology investigations.
  • Evaluation of factors modulating toxicity in clinical practice.

Main Results:

  • Local anesthetic toxicity involves cell death pathways (necrosis, apoptosis).
  • High concentrations and prolonged exposure increase lesion severity.
  • Metabolic alterations include sarcoplasmic reticulum and calcium dysregulation, mitochondrial dysfunction, and reactive oxygen species production.
  • Molecular targets include respiratory chain complex I and Akt kinase.

Conclusions:

  • Local anesthetics can cause significant histological damage to skeletal muscle.
  • Functional consequences in muscle and neurons require further investigation.
  • Optimizing clinical protocols and using adapted anesthetics for specific patient groups can reduce risks.
  • Preventive strategies like antioxidant drugs warrant further pharmacokinetic evaluation.

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