Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/107635
Title: Adenosine A2A Receptor Blockade Modulates Glucocorticoid-Induced Morphological Alterations in Axons, But Not in Dendrites, of Hippocampal Neurons
Authors: Pinheiro, Helena 
Gaspar, Rita 
Baptista, Filipa 
Fontes-Ribeiro, Carlos A. 
Ambrósio, Francisco 
Gomes, Catarina A. 
Keywords: dexamethasone; adenosine A2A receptor; development; hippocampal neurons; morphology
Issue Date: 2018
Publisher: Frontiers Media S.A.
Project: PEst UID/NEU/04539/2013 
POCI-01-0145-FEDER-007440 
CENTRO-01- 0145-FEDER-000008: BrainHealth 2020 
SFRH/BPD/86830/2012 
SFRH/BPD/86830/2012 
PD/BD/114116/2015 
Serial title, monograph or event: Frontiers in Pharmacology
Volume: 9
Issue: MAR
Abstract: The exposure to supra-physiological levels of glucocorticoids in prenatal life can lead to a long-term impact in brain cytoarchitecture, increasing the susceptibility to neuropsychiatric disorders. Dexamethasone, an exogenous glucocorticoid widely used in pregnant women in risk of preterm delivery, is associated with higher rates of neuropsychiatric conditions throughout life of the descendants. In animal models, prenatal dexamethasone exposure leads to anxious-like behavior and increased susceptibility to depressive-like behavior in adulthood, concomitant with alterations in neuronal morphology in brain regions implicated in the control of emotions and mood. The pharmacologic blockade of the purinergic adenosine A2A receptor, which was previously described as anxiolytic, is also able to modulate neuronal morphology, namely in the hippocampus. Additionally, recent observations point to an interaction between glucocorticoid receptors (GRs) and adenosine A2A receptors. In this work, we explored the impact of dexamethasone on neuronal morphology, and the putative implication of adenosine A2A receptor in the mediation of dexamethasone effects. We report that in vitro hippocampal neurons exposed to dexamethasone (250 nM), in the early phases of development, exhibit a polarized morphology alteration: dendritic atrophy and axonal hypertrophy. While the effect of dexamethasone in the axon is dependent on the activation of adenosine A2A receptor, the effect in the dendrites relies on the activation of GRs, regardless of the activation of adenosine A2A receptor. These results support the hypothesis of the interaction between GRs and adenosine A2A receptors and the potential therapeutic value of modulating adenosine A2A receptors activation in order to prevent glucocorticoid-induced alterations in developing neurons.
URI: https://hdl.handle.net/10316/107635
ISSN: 1663-9812
DOI: 10.3389/fphar.2018.00219
Rights: openAccess
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
I&D CIBB - Artigos em Revistas Internacionais
I&D ICBR - Artigos em Revistas Internacionais

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