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British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 1997 Jan 23;120(3):353–355. doi: 10.1038/sj.bjp.0700934

Volatile general anaesthetic actions on recombinant nAChα7, 5-HT3 and chimeric nAChα7-5-HT3 receptors expressed in Xenopus oocytes

Li Zhang 1,*, Murat Oz 1, Randall R Stewart 1, Robert W Peoples 1, Forrest F Weight 1
PMCID: PMC1564489  PMID: 9031735

Abstract

The effect of halothane and isoflurane was studied on the function of recombinant neurotransmitter receptors expressed in Xenopus oocytes. Both anaesthetics inhibited nicotinic acetylcholine type α7 (nAChα7) receptor-mediated responses, potentiated 5-hydroxytryptamine type 3 (5-HT3) receptor-mediated responses at low agonist concentrations, and inhibited the function of a chimeric receptor (with the N-terminal domain from the nAChα7 receptor and the transmembrane and C-terminal domains from the 5-HT3 receptor) in a manner similar to that of the nAChα7 receptor. Since the N-terminal domain of the chimeric receptor was from the nAChα7 receptor, the observations suggest that the inhibition involves the N-terminal domain of the receptor.

Keywords: Anaesthetics, receptors, ion channels, molecular chimera, acetylcholine receptor, 5-hydroxytryptamine receptor

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