British Journal of Anaesthesia, Vol 77, Issue 4 522-525, Copyright © 1996 by The Board of Management and Trustees of the British Journal of Anaesthesia
M. Dzoljic, W. Erdmann and M. R. Dzoljic
We have examined the role of benzodiazepine receptors in nitrous oxide-
induced neuronal depression in rats. The changes in neuronal excitability
induced by nitrous oxide and the benzodiazepine inverse agonist, Ro15-4513,
were monitored by measurement of visual evoked potentials (VEP).
Administration of Ro15-4513 10 mg kg-1 i.p., in rats breathing air, did not
affect the amplitude or latency of VEP. However, the same concentrations of
Ro15-4513 antagonized nitrous oxide-induced depression of VEP amplitudes.
We conclude that antagonism of nitrous oxide-induced depression by
Ro15-4513 indicates that at least part of the decreased neuronal
excitability caused by nitrous oxide could be ascribed to interactions with
the GABAA receptor complex.
LABORATORY INVESTIGATIONS
Visual evoked potentials and nitrous oxide-induced neuronal depression: role for benzodiazepine receptors
Department of Anaesthesiology, Academic Medical Centre, University of Amsterdam; Department of Anaesthesiology, University Hospital Dijkzigt; Department of Pharmacology, Erasmus University, Rotterdam, The Netherlands
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