Potential therapeutic interest of adenosine A2A receptors in psychiatric disorders

Detalhes bibliográficos
Autor(a) principal: Cunha, Rodrigo A.
Data de Publicação: 2008
Outros Autores: Ferré, Sergi, Vaugeois, Jean-Marie, Chen, Jiang-Fan
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/12670
https://doi.org/10.2174/138161208784480090
Resumo: The interest on targeting adenosine A(2A) receptors in the realm of psychiatric diseases first arose based on their tight physical and functional interaction with dopamine D(2) receptors. However, the role of central A(2A) receptors is now viewed as much broader than just controlling D(2) receptor function. Thus, there is currently a major interest in the ability of A(2A) receptors to control synaptic plasticity at glutamatergic synapses. This is due to a combined ability of A(2A) receptors to facilitate the release of glutamate and the activation of NMDA receptors. Therefore, A(2A) receptors are now conceived as a normalizing device promoting adequate adaptive responses in neuronal circuits, a role similar to that fulfilled, in essence, by dopamine. This makes A(2A) receptors particularly attractive targets to manage psychiatric disorders since adenosine may act as go-between glutamate and dopamine, two of the key players in mood processing. Furthermore, A(2A) receptors also control glia function and brain metabolic adaptation, two other emerging mechanisms to understand abnormal processing of mood, and A(2A) receptors are important players in controlling the demise of neurodegeneration, considered an amplificatory loop in psychiatric disorders. Current data only provide an indirect confirmation of this putative role of A(2A) receptors, based on the effects of caffeine (an antagonist of both A(1) and A(2A) receptors) in psychiatric disorders. However, the introduction of A(2A) receptors antagonists in clinics as anti-parkinsonian agents is hoped to bolster our knowledge on the role of A(2A) receptors in mood disorders in the near future
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spelling Potential therapeutic interest of adenosine A2A receptors in psychiatric disordersAdenosineA2A receptorCaffeineMood disordersPsychiatric diseasesAnxietyDepressionSchizophreniaAttention deficit hyperactivity disorderADHDThe interest on targeting adenosine A(2A) receptors in the realm of psychiatric diseases first arose based on their tight physical and functional interaction with dopamine D(2) receptors. However, the role of central A(2A) receptors is now viewed as much broader than just controlling D(2) receptor function. Thus, there is currently a major interest in the ability of A(2A) receptors to control synaptic plasticity at glutamatergic synapses. This is due to a combined ability of A(2A) receptors to facilitate the release of glutamate and the activation of NMDA receptors. Therefore, A(2A) receptors are now conceived as a normalizing device promoting adequate adaptive responses in neuronal circuits, a role similar to that fulfilled, in essence, by dopamine. This makes A(2A) receptors particularly attractive targets to manage psychiatric disorders since adenosine may act as go-between glutamate and dopamine, two of the key players in mood processing. Furthermore, A(2A) receptors also control glia function and brain metabolic adaptation, two other emerging mechanisms to understand abnormal processing of mood, and A(2A) receptors are important players in controlling the demise of neurodegeneration, considered an amplificatory loop in psychiatric disorders. Current data only provide an indirect confirmation of this putative role of A(2A) receptors, based on the effects of caffeine (an antagonist of both A(1) and A(2A) receptors) in psychiatric disorders. However, the introduction of A(2A) receptors antagonists in clinics as anti-parkinsonian agents is hoped to bolster our knowledge on the role of A(2A) receptors in mood disorders in the near futureBentham Science Publishers Ltd2008info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/12670http://hdl.handle.net/10316/12670https://doi.org/10.2174/138161208784480090engCurrent Pharmaceutical Design. 14:15 (2008) 1512-15241873-4286Cunha, Rodrigo A.Ferré, SergiVaugeois, Jean-MarieChen, Jiang-Faninfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-05-25T04:12:07Zoai:estudogeral.uc.pt:10316/12670Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:43:37.671541Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Potential therapeutic interest of adenosine A2A receptors in psychiatric disorders
title Potential therapeutic interest of adenosine A2A receptors in psychiatric disorders
spellingShingle Potential therapeutic interest of adenosine A2A receptors in psychiatric disorders
Cunha, Rodrigo A.
Adenosine
A2A receptor
Caffeine
Mood disorders
Psychiatric diseases
Anxiety
Depression
Schizophrenia
Attention deficit hyperactivity disorder
ADHD
title_short Potential therapeutic interest of adenosine A2A receptors in psychiatric disorders
title_full Potential therapeutic interest of adenosine A2A receptors in psychiatric disorders
title_fullStr Potential therapeutic interest of adenosine A2A receptors in psychiatric disorders
title_full_unstemmed Potential therapeutic interest of adenosine A2A receptors in psychiatric disorders
title_sort Potential therapeutic interest of adenosine A2A receptors in psychiatric disorders
author Cunha, Rodrigo A.
author_facet Cunha, Rodrigo A.
Ferré, Sergi
Vaugeois, Jean-Marie
Chen, Jiang-Fan
author_role author
author2 Ferré, Sergi
Vaugeois, Jean-Marie
Chen, Jiang-Fan
author2_role author
author
author
dc.contributor.author.fl_str_mv Cunha, Rodrigo A.
Ferré, Sergi
Vaugeois, Jean-Marie
Chen, Jiang-Fan
dc.subject.por.fl_str_mv Adenosine
A2A receptor
Caffeine
Mood disorders
Psychiatric diseases
Anxiety
Depression
Schizophrenia
Attention deficit hyperactivity disorder
ADHD
topic Adenosine
A2A receptor
Caffeine
Mood disorders
Psychiatric diseases
Anxiety
Depression
Schizophrenia
Attention deficit hyperactivity disorder
ADHD
description The interest on targeting adenosine A(2A) receptors in the realm of psychiatric diseases first arose based on their tight physical and functional interaction with dopamine D(2) receptors. However, the role of central A(2A) receptors is now viewed as much broader than just controlling D(2) receptor function. Thus, there is currently a major interest in the ability of A(2A) receptors to control synaptic plasticity at glutamatergic synapses. This is due to a combined ability of A(2A) receptors to facilitate the release of glutamate and the activation of NMDA receptors. Therefore, A(2A) receptors are now conceived as a normalizing device promoting adequate adaptive responses in neuronal circuits, a role similar to that fulfilled, in essence, by dopamine. This makes A(2A) receptors particularly attractive targets to manage psychiatric disorders since adenosine may act as go-between glutamate and dopamine, two of the key players in mood processing. Furthermore, A(2A) receptors also control glia function and brain metabolic adaptation, two other emerging mechanisms to understand abnormal processing of mood, and A(2A) receptors are important players in controlling the demise of neurodegeneration, considered an amplificatory loop in psychiatric disorders. Current data only provide an indirect confirmation of this putative role of A(2A) receptors, based on the effects of caffeine (an antagonist of both A(1) and A(2A) receptors) in psychiatric disorders. However, the introduction of A(2A) receptors antagonists in clinics as anti-parkinsonian agents is hoped to bolster our knowledge on the role of A(2A) receptors in mood disorders in the near future
publishDate 2008
dc.date.none.fl_str_mv 2008
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/12670
http://hdl.handle.net/10316/12670
https://doi.org/10.2174/138161208784480090
url http://hdl.handle.net/10316/12670
https://doi.org/10.2174/138161208784480090
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Current Pharmaceutical Design. 14:15 (2008) 1512-1524
1873-4286
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Bentham Science Publishers Ltd
publisher.none.fl_str_mv Bentham Science Publishers Ltd
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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