Potential therapeutic interest of adenosine A2A receptors in psychiatric disorders
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | , , |
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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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) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
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1799133707937775616 |