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dc.creatorPešić, Vesna
dc.creatorPetrović, Jelena
dc.creatorJukić, Marin
dc.date.accessioned2019-09-02T11:52:57Z
dc.date.available2019-09-02T11:52:57Z
dc.date.issued2016
dc.identifier.issn0272-4391
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/2625
dc.description.abstractThe emergence of rapid-acting antidepressants such as ketamine has motivated studies aiming to reveal the molecular mechanism of the ketamine antidepressant effect and to enable the clinical application of rapid-acting antidepressants. Here, we provide an overview of studies addressing the antidepressant effects of ketamine in depressed patients and animal models of depression and we compare the reduction of depressive symptoms in humans with the reduction in immobility time in the forced swim test in rodents after acute ketamine treatment. We also discuss different theories and potential biochemical pathways involved in the rapid antidepressant response to ketamine including the modulation of glutamatergic neurotransmission and intracellular hub-kinase activation. Finally, we summarize recent brain-region specific studies and we suggest that the activation of the ventral hippocampusmedial prefrontal cortexdorsal raphae nuclei (vHC-mPFC-DRN) neuronal pathway may mediate the antidepressant effect of ketamine. Although substantial progress has been made, further brain-region specific animal studies and longitudinal clinical trials are necessary for the understanding and successful application of novel rapid-acting antidepressants. Drug Dev Res 77 : 414-422, 2016.en
dc.publisherWiley, Hoboken
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/175036/RS//
dc.rightsrestrictedAccess
dc.sourceDrug Development Research
dc.titleMolecular Mechanism and Clinical Relevance of Ketamine as Rapid-Acting Antidepressanten
dc.typearticle
dc.rights.licenseARR
dcterms.abstractПешић, Весна; Јукић, Марин; Петровић, Јелена;
dc.citation.volume77
dc.citation.issue7
dc.citation.spage414
dc.citation.epage422
dc.citation.other77(7): 414-422
dc.citation.rankM23
dc.identifier.wos000387856500011
dc.identifier.doi10.1002/ddr.21335
dc.identifier.pmid27546787
dc.identifier.scopus2-s2.0-84994112380
dc.type.versionpublishedVersion


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