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dc.contributor.authorPilipenko, Vladimirs
dc.contributor.authorNarbute, Karina
dc.contributor.authorBeitnere, Ulrika
dc.contributor.authorRumaks, Juris
dc.contributor.authorPupure, Jolanta
dc.contributor.authorJansone, Baiba
dc.contributor.authorKlusa, Vija
dc.date.accessioned2019-12-02T18:55:35Z
dc.date.available2019-12-02T18:55:35Z
dc.date.issued2018-01-05
dc.identifier.citationAvailable online 11 November 2017 /en_US
dc.identifier.issn0014-2999
dc.identifier.urihttps://dspace.lu.lv/dspace/handle/7/49026
dc.description.abstractRecent studies devoted to neuroprotection have focused on the role of the gamma-aminobutyric acid (GABA) system in regulating neuroinflammatory processes which play a key role in the neurodegenerative processes observed in Alzheimer's disease (AD) by inducing glial cell overactivation and impairing neurotransmission. Data on the efficacy of classical GABA-A and GABA-B receptor agonists (muscimol and baclofen, respectively) in animal models of AD are not available. Moreover, no published studies have examined the ability of optimal doses of these compounds to prevent neuroinflammation, the alterations in neurotransmission and cognitive deficits. In the present study, we used a non-transgenic rat model of AD obtained by intracerebroventricular streptozocin (STZ) injection and assessed the effects of muscimol and baclofen at very low doses (0.01-0.05mg/kg) on spatial memory and the expression of cortical and hippocampal proteins related to neuroinflammation, namely proteins involved in astroglial functions (glial fibrillary acidic protein, GFAP), GABA synthesis (GABA synthesizing enzyme, glutamic acid decarboxylase 67, GAD67) and acetylcholine degradation (acetylcholine esterase). The presented study demonstrated that in a rat model of STZ-induced AD both muscimol and baclofen at the tested doses exerted memory-enhancing and anti-inflammatory effects, as well as normalization of acetylcholine esterase and GABA expression. We suggested that the function of very low doses of GABA receptor agonists differs from typical GABA-related inhibition and may be mediated by the allosteric sites of GABA receptors or other non-specific cell regulatory pathways.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.ispartofseriesEuropean Journal of Pharmacology;818
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBaclofenen_US
dc.subjectLearningen_US
dc.subjectMemoryen_US
dc.subjectMuscimolen_US
dc.subjectRat model of ADen_US
dc.subjectSTZen_US
dc.subjectResearch Subject Categories::MEDICINE::Physiology and pharmacology::Pharmacological researchen_US
dc.titleVery low doses of muscimol and baclofen ameliorate cognitive deficits and regulate protein expression in the brain of a rat model of streptozocin-induced Alzheimer's diseaseen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.identifier.doi10.1016/j.ejphar.2017.11.012


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