Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/83023
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dc.contributor.authorCollins-Praino, L.en
dc.contributor.authorGaltieri, D.en
dc.contributor.authorCollins, P.en
dc.contributor.authorJones, S.en
dc.contributor.authorPort, R.en
dc.contributor.authorPaul, N.en
dc.contributor.authorHockemeyer, J.en
dc.contributor.authorMuller, C.en
dc.contributor.authorSalamone, J.en
dc.date.issued2010en
dc.identifier.citationBehavioural Brain Research, 2010; 211(25):148-155en
dc.identifier.issn0166-4328en
dc.identifier.issn1872-7549en
dc.identifier.urihttp://hdl.handle.net/2440/83023-
dc.description.abstractForebrain dopamine (DA) is a critical component of the brain circuitry regulating behavioral activation. Adenosine A(2A) antagonists reverse many of the behavioral effects of DA antagonists, and A(2A) receptors are co-localized with D(2) receptors on striatal medium spiny neurons. The present work was undertaken to determine if the ability of an A(2A) antagonist, a non-selective adenosine antagonist, or an A(1) antagonist to reverse the locomotor effects of DA blockade in rats differed depending upon whether D(1) or D(2) family receptors were being antagonized. The adenosine antagonists MSX-3, caffeine, DPCPX and CPT were studied for their ability to reverse the locomotor suppression induced by the D(1) antagonist SCH 39166 (ecopipam) and the D(2) antagonist eticlopride. The D(1) and D(2) antagonists suppressed locomotion in all experiments. The adenosine A(2A) receptor antagonist MSX-3 (0.5-2.0 mg/kg IP) significantly reversed the suppression of locomotion induced by eticlopride. The non-selective adenosine antagonist caffeine (5.0-20.0 mg/kg IP) also reversed the effect of eticlopride, though the effect was not as robust as that seen with MSX-3. The adenosine A(1) antagonists DPCPX (0.375-1.5 mg/kg) and CPT (3.0-12.0 mg/kg IP) were unable to reverse the locomotor impairment elicited by eticlopride. Furthermore, the attenuation of locomotion induced by the D(1) antagonist could only be reversed by the highest dose of MSX-3, but not by caffeine, DPCPX or CPT. DA and adenosine receptor antagonists interact in the regulation of locomotor activation, but the nature of this interaction appears to depend upon the receptor selectivity profiles of the specific drugs being tested.en
dc.description.statementofresponsibilityLyndsey E. Collins, Daniel J. Galtieri, Patricia Collins, Shawnet K. Jones, Russell G. Port, Nicholas E. Paul, Jörg Hockemeyer, Christa E. Müller, John D. Salamoneen
dc.language.isoenen
dc.publisherElsevier Science BVen
dc.rights© 2010 Elsevier B.V. All rights reserved.en
dc.subjectProsencephalon; Animals; Rats; Rats, Sprague-Dawley; Receptors, Dopamine; Receptors, Purinergic P1; Dopamine Antagonists; Analysis of Variance; Behavior, Animal; Motor Activity; Dose-Response Relationship, Drug; Drug Interactions; Male; Purinergic P1 Receptor Antagonistsen
dc.titleInteractions between adenosine and dopamine receptor antagonists with different selectivity profiles: effects on locomotor activityen
dc.typeJournal articleen
dc.identifier.rmid0020137269en
dc.identifier.doi10.1016/j.bbr.2010.03.003en
dc.identifier.pubid14948-
pubs.library.collectionAnatomical Sciences publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidCollins-Praino, L. [0000-0002-4380-7600]en
Appears in Collections:Anatomical Sciences publications

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