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dc.contributor.authorDescombes, S.en
dc.contributor.authorAvoli, M.en
dc.contributor.authorPsarropoulou, C.en
dc.date.accessioned2015-11-24T16:31:55Z-
dc.date.available2015-11-24T16:31:55Z-
dc.identifier.issn0165-3806-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/7496-
dc.rightsDefault Licence-
dc.subjectadenosineen
dc.subjectdevelopmenten
dc.subjecthippocampusen
dc.subjectsynaptic inhibitionen
dc.subjectraten
dc.subjectguinea-pig hippocampusen
dc.subjectepileptiform activityen
dc.subjectendogenous adenosineen
dc.subjectpyramidal neuronsen
dc.subjectinduced epileptogenesisen
dc.subjectinvitroen
dc.subjectbrainen
dc.subjecttransmissionen
dc.subjectmechanismsen
dc.subjectreceptorsen
dc.titleA comparison of the adenosine-mediated synaptic inhibition in the CA3 area of immature and adult rat hippocampusen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondary<Go to ISI>://000076089000006-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0165380698000935/1-s2.0-S0165380698000935-main.pdf?_tid=8513389a-ad80-11e2-93c1-00000aab0f26&acdnat=1366878007_c70e6c7e7f16f98d3a5628aebe9fad35-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών και Τεχνολογιών. Τμήμα Βιολογικών Εφαρμογών και Τεχνολογιώνel
heal.publicationDate1998-
heal.abstractWe compared the effects of the adenosine Al receptor activation on the postsynaptic potentials (psps) recorded from the CA3 area of immature (postnatal days 10-20) and adult rat hippocampal neurons in vitro. The adenosine Al receptor agonist 2-phenyl-isopropyladenosine (PIA, 1 mu M) depressed the stimulus-induced psps less in immature and more in adult neurons. In the presence of the GABA, receptor antagonist bicuculline methiodide (BMI, 10 mu M), PIA reduced the duration and number of action potentials of the stimulus-induced paroxysmal depolarizations (PDs) in immature neurons, while it blocked PDs in adult neurons. Spontaneous BMI-induced PDs, were blocked by PLA in less than half (5/12) immature and all (6/6) adult neurons. The adenosine Al receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine (DPCPX, 1 mu M) enhanced the stimulus-induced psps in immature and adult neurons alike; this effect did not lead to stimulus-induced bursting in immature neurons. DPCPX induced spontaneous bursts (proconvulsant effect) in only 2/16 immature but in all adult (12/12) neurons. In BMI, DPCPX increased the duration and number of action potentials of the stimulus-induced PDs in immature and adult neurons alike (by about 30%), but it increased the rates of occurrence of spontaneous PDs in significantly more adult neurons. In conclusion, our results suggest that adenosine, acting via Al receptors, is a more effective endogenous anti-epileptic in adult than in immature hippocampus, a fact which may contribute to the susceptibility of the latter to epileptogenesis. (C) 1998 Elsevier Science B.V. All rights reserved.en
heal.journalNameDevelopmental Brain Researchen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά)

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