Influence of age on BDNF modulation of hippocampal synaptic transmission: Interplay with adenosine A2A receptors

We previously reported that adenosine, through A2A receptor activation, potentiates synaptic actions of brain‐derived neurotrophic factor (BDNF) in the hippocampus of infant (3–4 weeks) rats. Since A2A‐receptor‐mediated actions are more evident in old than in young rats and since the therapeutic pot...

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Published inHippocampus Vol. 17; no. 7; pp. 577 - 585
Main Authors Diógenes, Maria J., Assaife-Lopes, Natália, Pinto-Duarte, António, Ribeiro, Joaquim A., Sebastião, Ana M.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 2007
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Summary:We previously reported that adenosine, through A2A receptor activation, potentiates synaptic actions of brain‐derived neurotrophic factor (BDNF) in the hippocampus of infant (3–4 weeks) rats. Since A2A‐receptor‐mediated actions are more evident in old than in young rats and since the therapeutic potential for BDNF‐based strategies is greater in old subjects, we now evaluated synaptic actions of BDNF and the levels of TrkB receptors and of adenosine A2A receptors in the hippocampus of three groups of adult rats: young adults (10–16 weeks), old adults (36–38 weeks), and aged (70–80 weeks), as well as in one group of infant (3–4 weeks) rats. BDNF (20 ng/ml) enhances field excitatory postsynaptic potentials recorded from the hippocampus of young adults and aged rats, an action triggered by adenosine A2A receptor activation, since it was blocked by the A2A receptor antagonist, ZM 241385. In the other groups of animals BDNF (20 ng/ml) was virtually devoid of action on synaptic transmission. Western blot analysis of receptor density shows decreased amounts of TrkB receptors in old adults and aged rats, whereas A2A receptor levels assayed by ligand binding are enhanced in the hippocampus of old adults and aged rats. It is concluded that age‐related changes in the density of TrkB receptors and of adenosine A2A receptors may be responsible for a nonmonotonous variation of BDNF actions on synaptic transmission in the hippocampus. © 2007 Wiley‐Liss, Inc.
Bibliography:istex:CB71184AC294732866705D4B5617A8F5BC179B49
ark:/67375/WNG-HM6JRNCC-M
Fundação para a Ciência e Tecnologia and Fundação Calouste Gulbenkian
ArticleID:HIPO20294
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1050-9631
1098-1063
DOI:10.1002/hipo.20294