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dc.creatorHorvat, Anica
dc.creatorOrlić, T
dc.creatorBanjac, Ana
dc.creatorMomić, Tatjana
dc.creatorPetrović, S
dc.creatorDemajo, Miroslav
dc.date.accessioned2018-03-01T19:49:37Z
dc.date.available2018-03-01T19:49:37Z
dc.date.issued2006
dc.identifier.issn0231-5882
dc.identifier.urihttps://vinar.vin.bg.ac.rs/handle/123456789/3024
dc.description.abstractThe in vitro effect of digoxin, verapamil, propranolol, carbamazepine, diazepam and promethazine were investigated on the ecto-ATPase activity of synaptosomal plasma membranes from the rat brain. ATP hydrolyzing activities of the enzyme were not affected by digoxin while the use of all other drugs resulted in significant and dose-dependent ihibition in ATP hydrolysis. According to values Of IC50 and K-iapp, the order of inhibitory potency of the drugs applied was: diazepam GT promethazine GT verapamil GT propranolol GT GT carbamazepine. Kinetic analysis of the nature of the ATPase inhibition revealed that it resulted from a direct action of drugs on the enzyme protein. The aim of the present study was to determine the potential neuromodulatory side effects of the drugs investigated. The results achieved indicated that all investigated drugs, except digoxin, may modulate neuronal activities via the purinergic receptors P2 by increasing extracellular concentrations of ATP as a consequence of inhibition of the ecto-ATPase activity. Our findings indicate that it may be useful to take into consideration the possible side effects of the investigated drugs, when they are used in treatment of different pathologies, particularly in the treatment of epilepsy by carbamazepine and diazepam.en
dc.rightsrestrictedAccessen
dc.sourceGeneral Physiology and Biophysicsen
dc.subjectecto-ATPaseen
dc.subjectsynaptosomesen
dc.subjectdrugs raten
dc.titleInhibition of rat brain ecto-ATPase activity by various drugsen
dc.typearticleen
dcterms.abstractОрлиц, Т; Бањац, A; Петровиц, С; Демајо, М; Хорват, Aница; Момић Татјана;
dc.citation.volume25
dc.citation.issue1
dc.citation.spage91
dc.citation.epage105
dc.identifier.wos000237821600008
dc.citation.rankM23
dc.identifier.pmid16714778
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_vinar_3024


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