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dc.creatorTomić, Maja
dc.creatorVučković, Sonja M.
dc.creatorStepanović-Petrović, Radica
dc.creatorUgrešić, Nenad
dc.creatorProstran, Milica
dc.creatorBošković, Bogdan
dc.date.accessioned2019-09-02T11:07:54Z
dc.date.available2019-09-02T11:07:54Z
dc.date.issued2006
dc.identifier.issn0031-7144
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/858
dc.description.abstractIn this study we determined whether oxcarbazepine (OXC) could produce local peripheral antinociceptive effects in a rat model of inflammatory hyperalgesia, and whether adenosine receptors were involved. When coadministered with the pro-inflammatory compound concanavalin A, OXC (1000-3000 nmol/paw) caused a significant dose- and time-dependent anti-hyperalgesia. Caffeine (1000-1500 nmol/paw), a nonselective adenosine receptor antagonist, as well as 1,3-dipropyl-8-cyclopentylxanthine (DPCPX) (10-30 nmol/paw), a selective A, receptor antagonist, coadministered with OXC, significantly depressed its anti-hyperalgesic effect. Drugs injected into the contralateral hind paw did not produce significant effects. These results indicate that OXC produces local peripheral anti-hyperalgesic effects, which is mediated via peripheral A, receptors.en
dc.publisherGovi-Verlag Pharmazeutischer Verlag Gmbh, Eschborn
dc.rightsrestrictedAccess
dc.sourcePharmazie
dc.titlePeripheral anti-hyperalgesia by oxcarbazepine: involvement of adenosine A(1) receptorsen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractПростран, Милица; Вучковић, Соња М.; Бошковић, Богдан; Угрешић, Ненад; Томић, Маја; Степановић-Петровић, Радица;
dc.citation.volume61
dc.citation.issue6
dc.citation.spage566
dc.citation.epage568
dc.citation.other61(6): 566-568
dc.citation.rankM23
dc.identifier.wos000238320300016
dc.identifier.pmid16826981
dc.identifier.scopus2-s2.0-33745624612
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_farfar_858
dc.type.versionpublishedVersion


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