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

dc.contributor.authorJafarova Demirkapu, Mahluga
dc.contributor.authorYananli, Hasan Raci
dc.contributor.authorKaleli, Melisa
dc.contributor.authorSakalli, Halil Eren
dc.contributor.authorGoren, Mehmet Zafer
dc.contributor.authorTopkara, Betilay
dc.date.accessioned2026-02-06T18:50:53Z
dc.date.issued2020
dc.departmentDoğu Akdeniz Üniversitesi
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.description.sponsorshipMarmara Universitesi [SAG-C-TUP-141112-0331]
dc.description.sponsorshipMarmara Universitesi, Grant/Award Number: SAG-C-TUP-141112-0331
dc.identifier.doi10.1111/1440-1681.13224
dc.identifier.endpage560
dc.identifier.issn0305-1870
dc.identifier.issn1440-1681
dc.identifier.issue4
dc.identifier.orcid0000-0001-8717-4342
dc.identifier.orcid0000-0002-3509-9296
dc.identifier.orcid0000-0003-4649-3632
dc.identifier.orcid0000-0002-8800-4043
dc.identifier.pmid31808190
dc.identifier.scopus2-s2.0-85080836371
dc.identifier.scopusqualityQ2
dc.identifier.startpage553
dc.identifier.urihttps://doi.org/10.1111/1440-1681.13224
dc.identifier.urihttps://hdl.handle.net/11129/15103
dc.identifier.volume47
dc.identifier.wosWOS:000508566100001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofClinical and Experimental Pharmacology and Physiology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260204
dc.subjectadenosine
dc.subjectCPA
dc.subjectdopamine
dc.subjectmorphine
dc.subjectnoradrenaline
dc.subjectnucleus accumbens
dc.titleThe role of adenosine A1 receptors in the nucleus accumbens during morphine withdrawal
dc.typeArticle

Files