The role of adenosine A2A receptor activation during oxygen and glucose deprivation (OGD) was investigated on synaptic potentials (field excitatory post synaptic potentials, fEPSPs) extracellularly recorded from the dentate gyrus (DG). Nine min OGD elicited an irreversible loss of fEPSP and the appearance of anoxic depolarization (AD), a clear sign of brain damage. The selective adenosine A2A receptor antagonist, ZM241385 prevented AD appearance and allowed a significant recovery of neurotransmission after OGD. In addition, 9 min OGD facilitates neuroblast maturation, as indicated by immunohistochemical analysis.

The selective antagonism of A2A adenosine receptors prevents synaptic failure induced by oxygen and glucose deprivation in rat dentate gyrus / Maraula G.; Traini C.; Mello T.; Coppi E.; Galli A.; Pedata F.; Pugliese A.M.. - STAMPA. - (2013), pp. 255-258. (Intervento presentato al convegno 6th European Congress of Pharmacology tenutosi a Granada, Spain nel JUL 17-20, 2012).

The selective antagonism of A2A adenosine receptors prevents synaptic failure induced by oxygen and glucose deprivation in rat dentate gyrus

MARAULA, GIOVANNA;TRAINI, CHIARA;MELLO, TOMMASO;COPPI, ELISABETTA;GALLI, ANDREA;PEDATA, FELICITA;PUGLIESE, ANNA MARIA
2013

Abstract

The role of adenosine A2A receptor activation during oxygen and glucose deprivation (OGD) was investigated on synaptic potentials (field excitatory post synaptic potentials, fEPSPs) extracellularly recorded from the dentate gyrus (DG). Nine min OGD elicited an irreversible loss of fEPSP and the appearance of anoxic depolarization (AD), a clear sign of brain damage. The selective adenosine A2A receptor antagonist, ZM241385 prevented AD appearance and allowed a significant recovery of neurotransmission after OGD. In addition, 9 min OGD facilitates neuroblast maturation, as indicated by immunohistochemical analysis.
2013
PROCEEDINGS OF THE 6TH EUROPEAN CONGRESS OF PHARMACOLOGY
6th European Congress of Pharmacology
Granada, Spain
JUL 17-20, 2012
Maraula G.; Traini C.; Mello T.; Coppi E.; Galli A.; Pedata F.; Pugliese A.M.
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/803291
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