Clinical concentrations of chemically diverse general anesthetics minimally affect lipid bilayer properties Academic Article uri icon


MeSH Major

  • Anesthetics, Inhalation
  • Isoflurane
  • Nerve Tissue Proteins
  • Sodium Channel Blockers
  • Tetrodotoxin


  • General anesthetics have revolutionized medicine by facilitating invasive procedures, and have thus become essential drugs. However, detailed understanding of their molecular mechanisms remains elusive. A mechanism proposed over a century ago involving unspecified interactions with the lipid bilayer known as the unitary lipid-based hypothesis of anesthetic action, has been challenged by evidence for direct anesthetic interactions with a range of proteins, including transmembrane ion channels. Anesthetic concentrations in the membrane are high (10-100 mM), however, and there is no experimental evidence ruling out a role for the lipid bilayer in their ion channel effects. A recent hypothesis proposes that anesthetic-induced changes in ion channel function result from changes in bilayer lateral pressure that arise from partitioning of anesthetics into the bilayer. We examined the effects of a broad range of chemically diverse general anesthetics and related nonanesthetics on lipid bilayer properties using an established fluorescence assay that senses drug-induced changes in lipid bilayer properties. None of the compounds tested altered bilayer properties sufficiently to produce meaningful changes in ion channel function at clinically relevant concentrations. Even supra-anesthetic concentrations caused minimal bilayer effects, although much higher (toxic) concentrations of certain anesthetic agents did alter lipid bilayer properties. We conclude that general anesthetics have minimal effects on bilayer properties at clinically relevant concentrations, indicating that anesthetic effects on ion channel function are not bilayer-mediated but rather involve direct protein interactions.

publication date

  • March 21, 2017



  • Academic Article



  • eng

PubMed Central ID

  • PMC5373365

Digital Object Identifier (DOI)

  • 10.1073/pnas.1611717114

PubMed ID

  • 28265069

Additional Document Info

start page

  • 3109

end page

  • 3114


  • 114


  • 12