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Inhibition of Human α4β2 Neuronal Nicotinic Acetylcholine Receptors by Volatile Aromatic Anesthetics Depends on Drug Hydrophobicity
Author(s) -
Ken Solt,
Elizabeth Kelly,
Joseph F. Cotten,
Douglas E. Raines
Publication year - 2010
Publication title -
anesthesia and analgesia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.404
H-Index - 201
eISSN - 1526-7598
pISSN - 0003-2999
DOI - 10.1213/ane.0b013e3181c5f689
Subject(s) - pharmacology , nicotinic agonist , halothane , potency , hexafluorobenzene , receptor , anesthetic , intoxicative inhalant , gabaa receptor , medicine , acetylcholine , ion channel , acetylcholine receptor , nicotinic acetylcholine receptor , inhibitory postsynaptic potential , chemistry , biophysics , biochemistry , anesthesia , in vitro , toxicology , biology , organic chemistry , benzene
Volatile aromatic compounds such as benzene are general anesthetics that cause amnesia, hypnosis, and immobility in response to noxious stimuli when inhaled. Although these compounds are not used clinically, they are frequently found in commercial items such as solvents and household cleaning products and are abused as inhalant drugs. Volatile aromatic anesthetics are useful pharmacological tools for probing the relationship between chemical structure and drug activity at putative general anesthetic targets. Neuronal nicotinic acetylcholine (nACh) receptors are ligand-gated ion channels widely expressed in the brain, which are thought to play important roles in learning and memory. In this study, we tested the hypothesis that aromatic anesthetics reversibly inhibit alpha(4)beta(2) neuronal nACh receptor function and sought to determine the structural correlates of receptor inhibition.

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