Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
16
pubmed:dateCreated
2006-8-3
pubmed:abstractText
To locate the binding sites of general anesthetics on ligand-gated ion channels, two derivatives of the intravenous general anesthetic etomidate (2-ethyl 1-(phenylethyl)-1H-imidazole-5-carboxylate), in which the 2-ethyl group has been replaced by photoactivable groups based on either aryl diazirine or benzophenone chemistry, have been synthesized and characterized pharmacologically. TDBzl-etomidate (4-[3-(trifluoromethyl)-3H-diazirin-3-yl]benzyl 1-(1-phenylethyl)-1H-imidazole-5-carboxylate) and BzBzl-etomidate (4-benzoylbenzyl-1-(1-phenylethyl)-1H-imidazole-5-carboxylate are both potent general anesthetics with half-effective anesthetic concentrations of 700 and 220 nM, respectively. Both agents resembled etomidate in enhancing currents elicited by low concentrations of GABA on heterologously expressed GABAA receptors and in shifting the GABA concentration-response curve to lower concentrations. They also allosterically enhanced the binding of flunitrazepam to mammalian brain GABAA receptors. Both agents were also effective and selective photolabels, photoincorporating into some, but not all, subunits of the Torpedo nicotinic acetylcholine receptor to a degree that was allosterically regulated by an agonist or a noncompetitive inhibitor. Thus, they have the necessary pharmacological and photochemical properties to be useful in identifying the site of etomidate-induced anesthesia.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Anesthetics, General, http://linkedlifedata.com/resource/pubmed/chemical/Benzophenones, http://linkedlifedata.com/resource/pubmed/chemical/Diazomethane, http://linkedlifedata.com/resource/pubmed/chemical/Etomidate, http://linkedlifedata.com/resource/pubmed/chemical/GABA-A Receptor Agonists, http://linkedlifedata.com/resource/pubmed/chemical/Ion Channels, http://linkedlifedata.com/resource/pubmed/chemical/Ligands, http://linkedlifedata.com/resource/pubmed/chemical/Photoaffinity Labels, http://linkedlifedata.com/resource/pubmed/chemical/Protein Subunits, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, GABA-A, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Nicotinic, http://linkedlifedata.com/resource/pubmed/chemical/gamma-Aminobutyric Acid
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0022-2623
pubmed:author
pubmed:issnType
Print
pubmed:day
10
pubmed:volume
49
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4818-25
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:16884293-Allosteric Regulation, pubmed-meshheading:16884293-Anesthetics, General, pubmed-meshheading:16884293-Animals, pubmed-meshheading:16884293-Benzophenones, pubmed-meshheading:16884293-Brain, pubmed-meshheading:16884293-Cattle, pubmed-meshheading:16884293-Diazomethane, pubmed-meshheading:16884293-Etomidate, pubmed-meshheading:16884293-Female, pubmed-meshheading:16884293-GABA-A Receptor Agonists, pubmed-meshheading:16884293-Humans, pubmed-meshheading:16884293-Ion Channel Gating, pubmed-meshheading:16884293-Ion Channels, pubmed-meshheading:16884293-Larva, pubmed-meshheading:16884293-Ligands, pubmed-meshheading:16884293-Oocytes, pubmed-meshheading:16884293-Photoaffinity Labels, pubmed-meshheading:16884293-Protein Subunits, pubmed-meshheading:16884293-Receptors, GABA-A, pubmed-meshheading:16884293-Receptors, Nicotinic, pubmed-meshheading:16884293-Reflex, pubmed-meshheading:16884293-Torpedo, pubmed-meshheading:16884293-Xenopus laevis, pubmed-meshheading:16884293-gamma-Aminobutyric Acid
pubmed:year
2006
pubmed:articleTitle
Synthesis of trifluoromethylaryl diazirine and benzophenone derivatives of etomidate that are potent general anesthetics and effective photolabels for probing sites on ligand-gated ion channels.
pubmed:affiliation
Department of Anesthesia and Critical Care, Massachusetts General Hospital, Boston, Massachusetts 02114 USA.
pubmed:publicationType
Journal Article, In Vitro, Research Support, N.I.H., Extramural