Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2009-4-20
pubmed:abstractText
Deficits in N-methyl-D-aspartate receptor (NMDAR)-mediated neurotransmission may underlie dopaminergic hyperactivity in schizophrenia. Dysregulation of the GABAergic system has also been implicated. In this study we investigated a role for GABA(B) receptors as an intermediate step in the pathway leading from NMDAR stimulation to DA regulation. Since glycine (GLY) has been found to ameliorate treatment resistant negative symptoms in schizophrenia, we treated a group of rats with 16% GLY food for 2 weeks. DA levels in prefrontal cortex (PFC) and striatum (STR) were assessed by dual-probe microdialysis and HPLC-EC in freely moving rats. Infusion of the GABA(B) receptor agonists SKF97541 and baclofen into PFC and STR significantly reduced basal DA, an effect that was reversed by the antagonist, CGP52432. In PFC, GABA(B) agonists also reduced AMPH-induced DA release following treatment with either 1 or 5 mg/kg AMPH. Similar effects were seen following subchronic glycine treatment in the absence, but not presence of CGP52432 during 5 mg/kg AMPH treatment. In STR SKF97541 decreased only the 1 mg/kg AMPH-induced DA release. Subchronic GLY treatment in STR leads to a significant reduction in basal DA levels, but did not affect AMPH (5 mg/kg)-induced release. Our findings support a model in which NMDA/glycine-site agonists modulate DA release in part through presynaptic GABA(B) receptors on DA terminals, with both GABA(B) ligands and GLY significantly modulating AMPH-induced DA release. Both sites, therefore, may represent appropriate targets for drug development in schizophrenia and substance abuse disorders.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/3-aminopropyl(methyl)phosphinic acid, http://linkedlifedata.com/resource/pubmed/chemical/CGP 52608, http://linkedlifedata.com/resource/pubmed/chemical/GABA-B Receptor Agonists, http://linkedlifedata.com/resource/pubmed/chemical/GABA-B Receptor Antagonists, http://linkedlifedata.com/resource/pubmed/chemical/Ligands, http://linkedlifedata.com/resource/pubmed/chemical/Organophosphorus Compounds, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, GABA-B, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, N-Methyl-D-Aspartate, http://linkedlifedata.com/resource/pubmed/chemical/Thiazoles, http://linkedlifedata.com/resource/pubmed/chemical/Thiosemicarbazones, http://linkedlifedata.com/resource/pubmed/chemical/alpha-Amino-3-hydroxy-5-methyl-4-iso...
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1873-7064
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
56
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
915-21
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:19371582-Animals, pubmed-meshheading:19371582-Corpus Striatum, pubmed-meshheading:19371582-Dopamine, pubmed-meshheading:19371582-Extracellular Space, pubmed-meshheading:19371582-GABA-B Receptor Agonists, pubmed-meshheading:19371582-GABA-B Receptor Antagonists, pubmed-meshheading:19371582-Ligands, pubmed-meshheading:19371582-Male, pubmed-meshheading:19371582-Microdialysis, pubmed-meshheading:19371582-Organophosphorus Compounds, pubmed-meshheading:19371582-Prefrontal Cortex, pubmed-meshheading:19371582-Rats, pubmed-meshheading:19371582-Rats, Sprague-Dawley, pubmed-meshheading:19371582-Receptors, GABA-B, pubmed-meshheading:19371582-Receptors, N-Methyl-D-Aspartate, pubmed-meshheading:19371582-Thiazoles, pubmed-meshheading:19371582-Thiosemicarbazones, pubmed-meshheading:19371582-alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid
pubmed:year
2009
pubmed:articleTitle
GABAB/NMDA receptor interaction in the regulation of extracellular dopamine levels in rodent prefrontal cortex and striatum.
pubmed:affiliation
Nathan Kline Institute for Psychiatric Research, Orangeburg, NY 10962, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural