British Journal of Anaesthesia, Vol 76, Issue 5 702-706, Copyright © 1996 by The Board of Management and Trustees of the British Journal of Anaesthesia
T. Goto, JJA. Marota and G. Crosby
We reported previously that nitrous oxide induces pre-emptive analgesia
that is partially antagonized by naloxone and totally antagonized by
halothane. The aims of this study were to determine if halothane and
isoflurane are similar in this respect and to examine if volatile
anaesthetics antagonize the analgesic effect of exogenous opioids. We found
that 75% nitrous oxide prolonged tail-flick latency by 37% and this
analgesia was dose-dependently inhibited by halothane and, less
effectively, by isoflurane. In contrast, morphine 1.25 mg kg-1 i.v. also
prolonged tail-flick latency by 35% but, unlike nitrous oxide- induced
analgesia, this effect was attenuated only by high doses of halothane and
was unaffected by isoflurane. Neither halothane nor isoflurane alone
altered the tail-flick response. We conclude that both halothane and
isoflurane dose-dependently antagonized nitrous oxide analgesia but
antagonized morphine-induced analgesia to a lesser extent.
LABORATORY INVESTIGATIONS
Volatile anaesthetics antagonize nitrous oxide and morphine-induced analgesia in the rat
Anesthesia Services, Massachusetts General Hospital and Department of Anaesthesia, Harvard Medical School, Boston, MA 02114, USA
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