Publication:
The role of adenosine A1 receptors in the nucleus accumbens during morphine withdrawal

dc.contributor.authorYANANLI, HASAN RACİ
dc.contributor.authorGÖREN, MEHMET ZAFER
dc.contributor.authorsJafarova Demirkapu, Mahluga; Yananli, Hasan Raci; Kaleli, Melisa; Sakalli, Halil Eren; Goren, Mehmet Zafer; Topkara, Betilay
dc.date.accessioned2022-03-12T22:44:26Z
dc.date.accessioned2026-01-11T19:05:05Z
dc.date.available2022-03-12T22:44:26Z
dc.date.issued2020
dc.description.abstractOpioids are effective analgaesic agents, but serious adverse effects such as tolerance and withdrawal contribute to opioid dependence and limit their use. Opioid withdrawal is a common occurrence in human opiate addicts that is not life-threatening. Studies have shown that the mesocorticolimbic system, especially the nucleus accumbens, is an important region in drug addiction and adenosine receptors play a modulatory role in the mechanism of action of drug dependence and withdrawal. The aim of this study was to investigate the effects of the selective A(1) receptor agonist CPA (N-6-cyclopentyladenosine) on withdrawal symptoms, and the concentration of dopamine and noradrenaline in the nucleus accumbens and locomotor activity behaviour during naloxone-precipitated withdrawal in morphine-dependent rats. The local administration of CPA (1.5, 3.0, and 6.0 mmol/L bilateral 250 nL) into the nucleus accumbens decreased the Gellert-Holtzman withdrawal scale, and increased concentrations of dopamine and noradrenaline in the same region during naloxone-induced withdrawal. Our findings suggest that administration of the A(1) receptor agonist significantly decreased withdrawal behaviours and increased dopamine and noradrenaline concentrations in opioid withdrawal in a dose-dependent manner. These results demonstrate that adenosine receptors should be examined as a potential mechanism that could be exploited for the treatment of morphine withdrawal.
dc.identifier.doi10.1111/1440-1681.13224
dc.identifier.eissn1440-1681
dc.identifier.issn0305-1870
dc.identifier.pubmed31808190
dc.identifier.urihttps://hdl.handle.net/11424/236429
dc.identifier.wosWOS:000508566100001
dc.language.isoeng
dc.publisherWILEY
dc.relation.ispartofCLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectadenosine
dc.subjectCPA
dc.subjectdopamine
dc.subjectmorphine
dc.subjectnoradrenaline
dc.subjectnucleus accumbens
dc.subjectADENOSINE A(1) RECEPTORS
dc.subjectD-ASPARTATE RECEPTOR
dc.subjectSYNAPTIC-TRANSMISSION
dc.subjectMEDIATED MODULATION
dc.subjectOPIATE WITHDRAWAL
dc.subjectPREFRONTAL CORTEX
dc.subjectDOPAMINE RELEASE
dc.subjectA(2A) RECEPTORS
dc.subjectGABA RELEASE
dc.subjectRAT
dc.titleThe role of adenosine A1 receptors in the nucleus accumbens during morphine withdrawal
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage560
oaire.citation.issue4
oaire.citation.startPage553
oaire.citation.titleCLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY
oaire.citation.volume47

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