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dc.contributor.authorSadigh-Eteghad, S
dc.contributor.authorMahmoudi, J
dc.contributor.authorBabri, S
dc.contributor.authorTalebi, M
dc.date.accessioned2018-08-26T07:41:40Z
dc.date.available2018-08-26T07:41:40Z
dc.date.issued2015
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/47613
dc.description.abstractPURPOSE: To evaluate the effects of PHA-543613 (alpha 7-nAChR agonist) and galantamine (acetylcholinesterase inhibitor (AChEI)) on recognition memory and neurovascular coupling (NVC) response in beta-amyloid (A beta)(25-35)-treated mice. METHODS: PHA-543613 (1 mg/kg, i.p.), and galantamine (3 mg/kg, s.c.), effects were tested in A beta(25-35) mice model of AD. alpha 7-nAChR antagonist, methyllycaconitine (MLA) (1 mg/kg, i.p.), was used for evaluation of receptor blockade effects. Recognition memory in animals was assessed by the novel object recognition (NOR) task. NVC response was analyzed by laser-doppler flow meter in barrel cortex by whisker stimulation method. RESULTS: Both, PHA-543613 and galantamine improve recognition memory in A beta-treated animals. However, the advantageous effects of PHA-543613 were significantly higher than galantamine. Also, pretreatment with MLA reversed both galantamine and PHA-543613 effects on NOR. Impaired NVC response in AD animals was improved by PHA-543613 and galantamine. However, MLA pretreatment disrupts this function. CONCLUSION: Activation of alpha 7-nAChR improved recognition memory possible through enhancement of neurovascular response in Alzheimer's disease in animals.
dc.language.isoEnglish
dc.relation.ispartofACTA CIRURGICA BRASILEIRA
dc.subjectAmyloid beta-Peptides
dc.subjectRecognition
dc.subjectReceptors, Nicotinic
dc.subjectMice
dc.titleEffect of alpha-7 nicotinic acetylcholine receptor activation on beta-amyloid induced recognition memory impairment. Possible role of neurovascular function
dc.typeArticle
dc.citation.volume30
dc.citation.issue11
dc.citation.spage736
dc.citation.epage742
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1590/S0102-865020150110000003


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