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dc.contributor.authorIravani, Mahmoud M.
dc.contributor.authorKruk, Z. L.
dc.date.accessioned2014-02-27T13:58:58Z
dc.date.available2014-02-27T13:58:58Z
dc.date.issued1996-03
dc.identifier.citationIravani , M M & Kruk , Z L 1996 , ' Real-time effects of N-methyl-D-aspartic acid on dopamine release in slices of rat caudate putamen : A study using fast cyclic voltammetry ' , Journal of Neurochemistry (JNC) , vol. 66 , no. 3 , pp. 1076-1085 . https://doi.org/10.1046/j.1471-4159.1996.66031076.x
dc.identifier.issn0022-3042
dc.identifier.otherORCID: /0000-0002-4905-9682/work/32997609
dc.identifier.urihttp://hdl.handle.net/2299/12950
dc.description.abstractThe functional role of N-methyl-D-aspartic acid (NMDA) glutamate receptors in the real-time regulation of single electrical pulse (1 p)-stimulated endogenous dopamine release was investigated in slices of rat caudate putamen using fast cyclic voltammetry at a carbon fibre electrode. In the presence of Mg2+, 20 mu M NMDA had a weak effect on background signals but did not affect 1 p-stimulated dopamine release. Removal of Mg2+ increased the background and doubled 1 p-stimulated dopamine release. In the absence of Mg2+, 20 mu M NMDA caused a transient ''release'' of dopamine and decreased the background signal. The 1 p-stimulated dopamine release was subsequently reduced. In the presence of 1 mu M (+/-)-3-(2-carboxypiperazin-4-yl)-propyl-1-phosphonic acid (CPP), superfusion with 20 mu M NMDA did not cause a transient ''release'' of dopamine, and 1 p-stimulated dopamine release was not subsequently attenuated. In the presence of 1 mu M tetrodotoxin, 1 p-stimulated dopamine release was abolished, but 20 mu M NMDA still caused a transient ''release'' of dopamine. Removal of Ca2+ from the artificial CSF abolished 1 p-stimulated dopamine release and resulted in a decline in the baseline but did not affect dopamine ''release'' when 20 mu M NMDA was added, The dopamine release-inducing effect of 20 mu M NMDA was less pronounced in sites in the caudate putamen where dopamine release increased with frequency of electrical stimulation (hot spots) than in sites where there was little frequency-dependent dopamine release (cold spots). Subsequent 1 p-stimulated dopamine release was less attenuated in cold spots than in hot spots. We conclude that in the absence of Mg2+, NMDA induces release of dopamine by acting at CPP-sensitive NMDA receptors in a Ca2+-independent manner. This transient release depletes dopamine from a storage site from which dopamine is released by 1 p electrical stimulation. These real-time observations of the effects of NMDA on electrical stimulus-independent and -dependent dopamine release may explain the apparently conflicting observations of the effects of NMDA on dopamine release made in previous studies, They also indicate that dopamine release and storage are heterogeneous at different sites in the rat caudate putamen.en
dc.format.extent10
dc.language.isoeng
dc.relation.ispartofJournal of Neurochemistry (JNC)
dc.subjectNMDA
dc.subjectdopamine release
dc.subjectcaudate putamen
dc.subjectfast cyclic voltammetry
dc.subjectelectrical stimulation
dc.subjectNMDA receptor antagonist
dc.subjectINVIVO PRESYNAPTIC CONTROL
dc.subjectEXCITATORY AMINO-ACIDS
dc.subjectNMDA-EVOKED RELEASE
dc.subjectSTRIATAL SLICES
dc.subjectL-GLUTAMATE
dc.subjectBRAIN-SLICES
dc.subjectNUCLEUS-ACCUMBENS
dc.subjectH-3 DOPAMINE
dc.subjectNITRIC-OXIDE
dc.subjectEXTRACELLULAR DOPAMINE
dc.titleReal-time effects of N-methyl-D-aspartic acid on dopamine release in slices of rat caudate putamen : A study using fast cyclic voltammetryen
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionCentre for Research in Mechanisms of Disease and Drug Discovery
dc.contributor.institutionDepartment of Clinical, Pharmaceutical and Biological Science
dc.contributor.institutionBasic and Clinical Science Unit
dc.contributor.institutionCentre for Health Services and Clinical Research
dc.description.statusPeer reviewed
rioxxterms.versionofrecord10.1046/j.1471-4159.1996.66031076.x
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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