Neurotoxicity associated with colistin methanesulfonate treatment is enhanced by concomitant sevoflurane inhalation

Mai Gotoda1, Yuki Enoki1, Shino Shishido1

  • 1Division of Pharmacodynamics, Keio University Faculty of Pharmacy, 1-5-30 Shibakoen, Minato-ku, Tokyo 105-8512, Japan.

Toxicology Reports
|December 15, 2022
PubMed

Insights

Sevoflurane enhances colistin methanesulfonate (CMS) neurotoxicity, increasing neuromuscular blockade. Combining CMS with sevoflurane significantly lowers the inhibitory dose, suggesting clinical caution is needed.

Area of Science:

  • Pharmacology
  • Neuroscience
  • Anesthesiology

Background:

  • Colistin methanesulfonate (CMS) is a polypeptide antibiotic known for neurotoxic side effects.
  • Sevoflurane (Sevo), an inhaled anesthetic, is suspected to potentiate neuromuscular relaxants, but its mechanism is unclear.
  • The interaction between CMS and sevoflurane regarding neurotoxicity requires investigation.

Purpose of the Study:

  • To investigate the augmenting effect of sevoflurane on colistin methanesulfonate-induced neurotoxicity.
  • To evaluate the relationship between pharmacokinetic parameters and neuromuscular inhibitory effects.

Main Methods:

  • A sciatic nerve-skeletal muscle stimulation model was used in Sprague-Dawley male rats.
  • Rats were administered CMS with or without sevoflurane.
  • Electromyogram measurements determined the muscle contraction inhibition rate; pharmacokinetic simulations were performed.

Main Results:

  • Sevoflurane demonstrated a dose-dependent augmentation of CMS-induced neuromuscular inhibition.
  • The 50% inhibitory dose (ID50) for CMS was reduced by 49% when combined with sevoflurane (85 ± 5 mg/kg vs. 167 ± 12 mg/kg).
  • Simulated pharmacokinetic analysis indicated lower predicted AUC values for colistin at ID50 with sevoflurane co-administration.

Conclusions:

  • Concomitant use of sevoflurane significantly enhances the neurotoxic effects of colistin methanesulfonate.
  • The observed potentiation suggests a potential for increased neurotoxicity in clinical settings.
  • Avoidance of combined CMS and sevoflurane administration is recommended.

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