Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/5979
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dc.contributor.authorKerr, D.en
dc.contributor.authorOng, J.en
dc.date.issued2003en
dc.identifier.citationEuropean Journal of Pharmacology, 2003; 468(2):103-108en
dc.identifier.issn0014-2999en
dc.identifier.issn1879-0712en
dc.identifier.urihttp://hdl.handle.net/2440/5979-
dc.description.abstractSelected neutral L-alpha-amino acids, and their dipeptides, were reversible, stereospecific, potentiators of GABA(B) receptor-mediated hyperpolarizing responses to baclofen (3-100 microM) in rat neocortical slices. These responses were sensitive to the GABA(B) receptor antagonist (+)-(S)-5,5-dimethylmorpholinyl-2-acetic acid (Sch50911) (30 microM). Most potent were L-Leu, L-Ile and L-Phe, as were the dipeptides L-Phe-Phe and L-Phe-Leu, and less potent were L-Met, L-Val, L-Cys, L-Cystine, L-Tyr, L-Thr, L-Arg and L-Ser. Inactive were L-Trp, L-His, L-Lys and L-Pro. These potentiators gave leftward shifts of the baclofen concentration-response curves with a Hill slope of 2, and a marked increase in the maximal hyperpolarizing responses. Selected L-amino acids and dipeptides are a class of naturally occurring GABA(B) potentiators, which may be allosteric modulators.en
dc.language.isoenen
dc.publisherElsevier Science BVen
dc.subjectNeocortex; Animals; Rats; Rats, Sprague-Dawley; Baclofen; Amino Acids; Dipeptides; GABA Agonists; Allosteric Regulation; Dose-Response Relationship, Drug; Drug Synergism; Stereoisomerism; Male; GABA-B Receptor Agonistsen
dc.titlePotentiation of metabotropic GABAB receptors by L-amino acids and dipeptides in rat neocortexen
dc.typeJournal articleen
dc.identifier.rmid0020030626en
dc.identifier.doi10.1016/s0014-2999(03)01675-3en
dc.identifier.pubid58709-
pubs.library.collectionAnaesthesia and Intensive Care publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
Appears in Collections:Anaesthesia and Intensive Care publications

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