Free
Correspondence  |   February 1999
Plus Ca Change 
Author Notes
  • Department of Anesthesia and Critical Care CLN-3; Massachusetts General Hospital; Boston, Massachusetts 02114;
Article Information
Correspondence
Correspondence   |   February 1999
Plus Ca Change 
Anesthesiology 2 1999, Vol.90, 632. doi:
Anesthesiology 2 1999, Vol.90, 632. doi:
In Reply:-We appreciate the comments of Dr. Cohen and his experimental contributions to understanding the molecular and cellular mechanisms of anesthetic compounds and their relatives. Indeed, we are reminded that exceptions to the Meyer-Overton solubility rule have been identified for more than half a century, including helium and neon, compounds beyond the “cut-off” length in several molecular families, some perfluroalkanes and sulfur hexafluoride, and the relatively recently described “nonanesthetic” volatile compounds. [1,2] These compounds, some of which are convulsants, are critically important to testing models of anesthetic mechanisms, because robust hypotheses should account for both anesthetic potency and the inactivity of compounds that do not cause anesthesia.
Despite advances in neurobiology and the incorporation of molecular biology in studies of anesthesia, a testable hypothesis that convincingly links the molecular interactions of anesthetics with behavioral effects in animals is still lacking. Putative targets that affect the activity of neurons include ligand-gated ion channels, such as the gamma-aminobutyric acid type A (GABAA) receptor, glycine receptors, and N-ethyl-D-apartate receptors, but how the functions of these dynamic macromolecules are modulated by anesthetics remains unknown. One popular idea, based on the now classic Franks and Lieb [3] studies of lipid-free firefly luciferase, is that anesthetics act by interacting directly with protein sites. Can such sites distinguish between an anesthetic molecule and a nonanesthetic one? Our study [4] explored this question using experimental protein models in which direct interactions between anesthetic molecules and proteins have been established.
Our results indicate that known hydrophobic protein sites, such as the ion channel of the nicotinic acetylcholine receptor and human serum albumin, do a poor job or discriminating nonanesthetic from anesthetic compounds. However, our results also suggest that these compounds may differ in their ability to reach binding sites that alter protein function. We look forward to using molecular biophysical methods in future experiments on putative anesthetic target proteins. Such approaches may establish the existence of functional anesthetic binding sites on these targets, leading us another step closer to a robust hypothesis.
Stuart A. Forman, M.D., Ph.D.
Douglas E. Raines, M.D.
Department of Anesthesia and Critical Care CLN-3; Massachusetts General Hospital; Boston, Massachusetts 02114;
(Accepted for publication October 12, 1998.)
REFERENCES
Miller KW: The nature of the site of general anesthesia [review]. Int Rev Neurobiol 1985; 27:1-61
Koblin DD, Chortkoff BS, Laster MJ, Eger EI II, Halsey MJ, Ionescu P: Polyhalogenated and perfluorinated compounds that disobey the Meyer-Overton hypothesis. Anesth Analg 1994; 79:1043-8
Franks NP, Lieb WR: Do general anesthetics act by competitive binding to specific receptors? Nature 1984; 310:599-601
Forman SA, Raines DE: Nonanesthetic volatile drugs obey the Meyer-Overton correlation in two molecular protein site models. Anesthesiology 1998; 88:1535-48