Anesth Analg 2005;101:131-135
© 2005 International Anesthesia Research Society
doi: 10.1213/01.ANE.0000153011.64764.6F
ANESTHETIC PHARMACOLOGY
R (+) Etomidate and the Photoactivable R (+) Azietomidate Have Comparable Anesthetic Activity in Wild-Type Mice and Comparably Decreased Activity in Mice with a N265M Point Mutation in the Gamma-Aminobutyric Acid Receptor ß3 Subunit
Mark Liao, BS,
James M. Sonner, MD,
S. Shaukat Husain, DPhil*,
Keith W. Miller, DPhil*,
Rachel Jurd, PhD ,
Uwe Rudolph, MD , and
Edmond I. Eger, II, MD
Department of Anesthesia and Perioperative Care, University of California, San Francisco, California; *Department of Anesthesia and Critical Care, Massachusetts General Hospital, Boston, Massachusetts; and Institute of Pharmacology and Toxicology, University of Zurich, Zurich, Switzerland
Address correspondence to Edmond I Eger II, MD, Department of Anesthesia, S-455, University of California, San Francisco, CA 941430464. Address e-mail to egere{at}anesthesia.ucsf.edu.
A photoactivable diazirine derivative of etomidate, azietomidate, shares many actions of etomidate, including a capacity to abolish the righting reflexes in tadpoles and enhance gamma-aminobutyric acid (GABA)-induced currents. Azietomidates usefulness in studies of mechanisms of anesthesia depends on the assumption that it shares a site of action with etomidate. Mice bearing an N265M ß3 subunit point mutation in GABAA receptors have a markedly decreased sensitivity to loss of righting reflexes induced by etomidate over a range of doses. Accordingly, in the present study we measured the time to recovery of righting reflexes of wild type and mutant mice as a function of dose given as an IV bolus. Analysis of the data for azietomidate yielded mean times to recovery of righting reflexes at a dose of 7.5 mg/kg of 10.0 ± 0.9 min and 3.0 ± 1.6 min for wild type and mutant mice, respectively (mean ± sd). A similar analysis for etomidate yielded mean times to recovery of righting reflexes at a dose of 7.5 mg/kg of 12.0 ± 1.3 min and 4.0 ± 0.7 min for wild type and mutant mice respectively. Thus, at this dose a single mutation, N265M on the ß3 subunit of the GABAA receptor, approximately halved the time to recovery of righting reflexes for both etomidate and azietomidate (by 7.6 ± 1.5 min and 7.2 ± 1.8 min, respectively), emphasizing the contribution of this residue as a determinant of a behavioral response of azietomidate in mice.
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