Transducing system operated by adenosine A2A receptors to facilitate acetylcholine release in the rat hippocampus
Autor(a) principal: | |
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Data de Publicação: | 2002 |
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/10316/4819 https://doi.org/10.1016/S0014-2999(02)02475-5 |
Resumo: | Although molecular biology studies indicate the presence of adenosine A2A receptors in the rat hippocampus, the pharmacological characterization of adenosine A2A receptor binding and of its putative facilitatory effects has revealed features essentially different from these found for adenosine A2A receptors in most preparations. We now confirmed that activation of adenosine A2A receptors with 2-[4-(2-p-carboxyethyl)phenylamino]-5'-N-ethylcarboxamidoadenosine (CGS 21680, 1-30 nM) or 2-hexynyl-5'-N-ethylcarboxamidoadenosine (HENECA, 3-100 nM) facilitated the veratridine-evoked [3H]acetylcholine release from hippocampal synaptosomes with a maximal effect of 14±2% and 16±2%, respectively. These effects were prevented by the adenosine A2A receptor antagonists, 4-(2-[7-amino-2-{2-furyl}{1,2,4}-triazolo{2,3a}{1,3,5}triazin-5-yl-amino]ethyl)phenol (ZM 241385, 20 nM) and 5-amino-7-(2-phenylethyl)-2-(2-furyl)-pyrazolo-[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine (SCH 58261, 20 nM), but not by the adenosine A1 receptor antagonist, 1,3-dipropyl-8-cyclopentylxanthine (DPCPX, 20 nM). Adenosine A2A receptors may activate adenylate cyclase and protein kinase A since CGS 21680 (10 nM) facilitation of [3H]acetylcholine release was occluded by 8-bromo-cAMP (0.5 mM) and forskolin (10 [mu]M) and prevented by H-89 (1 [mu]M), but unaffected by phorbol-12,13-didecanoate (250 nM) or bisindolylmaleimide I (1 [mu]M). The existence of adenosine A2A receptors in hippocampal nerve terminals was further confirmed by a Western blot immunoreactivity qualitatively identical to that found in the striatum. This constitutes the first pharmacological identification of canonical adenosine A2A receptors coupling to the expected cAMP/protein kinase A pathway in the hippocampus with the expected immunoreactivity. |
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Transducing system operated by adenosine A2A receptors to facilitate acetylcholine release in the rat hippocampusAdenosineA2A receptorHippocampusAcetylcholine releaseNerve terminalSynaptosomeAlthough molecular biology studies indicate the presence of adenosine A2A receptors in the rat hippocampus, the pharmacological characterization of adenosine A2A receptor binding and of its putative facilitatory effects has revealed features essentially different from these found for adenosine A2A receptors in most preparations. We now confirmed that activation of adenosine A2A receptors with 2-[4-(2-p-carboxyethyl)phenylamino]-5'-N-ethylcarboxamidoadenosine (CGS 21680, 1-30 nM) or 2-hexynyl-5'-N-ethylcarboxamidoadenosine (HENECA, 3-100 nM) facilitated the veratridine-evoked [3H]acetylcholine release from hippocampal synaptosomes with a maximal effect of 14±2% and 16±2%, respectively. These effects were prevented by the adenosine A2A receptor antagonists, 4-(2-[7-amino-2-{2-furyl}{1,2,4}-triazolo{2,3a}{1,3,5}triazin-5-yl-amino]ethyl)phenol (ZM 241385, 20 nM) and 5-amino-7-(2-phenylethyl)-2-(2-furyl)-pyrazolo-[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine (SCH 58261, 20 nM), but not by the adenosine A1 receptor antagonist, 1,3-dipropyl-8-cyclopentylxanthine (DPCPX, 20 nM). Adenosine A2A receptors may activate adenylate cyclase and protein kinase A since CGS 21680 (10 nM) facilitation of [3H]acetylcholine release was occluded by 8-bromo-cAMP (0.5 mM) and forskolin (10 [mu]M) and prevented by H-89 (1 [mu]M), but unaffected by phorbol-12,13-didecanoate (250 nM) or bisindolylmaleimide I (1 [mu]M). The existence of adenosine A2A receptors in hippocampal nerve terminals was further confirmed by a Western blot immunoreactivity qualitatively identical to that found in the striatum. This constitutes the first pharmacological identification of canonical adenosine A2A receptors coupling to the expected cAMP/protein kinase A pathway in the hippocampus with the expected immunoreactivity.http://www.sciencedirect.com/science/article/B6T1J-4712SFJ-1/1/afef5149e7c76af1755d92952b64b16e2002info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttp://hdl.handle.net/10316/4819http://hdl.handle.net/10316/4819https://doi.org/10.1016/S0014-2999(02)02475-5engEuropean Journal of Pharmacology. 454:1 (2002) 31-38Rebola, NelsonOliveira, Catarina R.Cunha, Rodrigo A.info: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:RCAAP2020-11-06T16:59:30Zoai:estudogeral.uc.pt:10316/4819Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:43:28.599996Repositório 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 |
Transducing system operated by adenosine A2A receptors to facilitate acetylcholine release in the rat hippocampus |
title |
Transducing system operated by adenosine A2A receptors to facilitate acetylcholine release in the rat hippocampus |
spellingShingle |
Transducing system operated by adenosine A2A receptors to facilitate acetylcholine release in the rat hippocampus Rebola, Nelson Adenosine A2A receptor Hippocampus Acetylcholine release Nerve terminal Synaptosome |
title_short |
Transducing system operated by adenosine A2A receptors to facilitate acetylcholine release in the rat hippocampus |
title_full |
Transducing system operated by adenosine A2A receptors to facilitate acetylcholine release in the rat hippocampus |
title_fullStr |
Transducing system operated by adenosine A2A receptors to facilitate acetylcholine release in the rat hippocampus |
title_full_unstemmed |
Transducing system operated by adenosine A2A receptors to facilitate acetylcholine release in the rat hippocampus |
title_sort |
Transducing system operated by adenosine A2A receptors to facilitate acetylcholine release in the rat hippocampus |
author |
Rebola, Nelson |
author_facet |
Rebola, Nelson Oliveira, Catarina R. Cunha, Rodrigo A. |
author_role |
author |
author2 |
Oliveira, Catarina R. Cunha, Rodrigo A. |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Rebola, Nelson Oliveira, Catarina R. Cunha, Rodrigo A. |
dc.subject.por.fl_str_mv |
Adenosine A2A receptor Hippocampus Acetylcholine release Nerve terminal Synaptosome |
topic |
Adenosine A2A receptor Hippocampus Acetylcholine release Nerve terminal Synaptosome |
description |
Although molecular biology studies indicate the presence of adenosine A2A receptors in the rat hippocampus, the pharmacological characterization of adenosine A2A receptor binding and of its putative facilitatory effects has revealed features essentially different from these found for adenosine A2A receptors in most preparations. We now confirmed that activation of adenosine A2A receptors with 2-[4-(2-p-carboxyethyl)phenylamino]-5'-N-ethylcarboxamidoadenosine (CGS 21680, 1-30 nM) or 2-hexynyl-5'-N-ethylcarboxamidoadenosine (HENECA, 3-100 nM) facilitated the veratridine-evoked [3H]acetylcholine release from hippocampal synaptosomes with a maximal effect of 14±2% and 16±2%, respectively. These effects were prevented by the adenosine A2A receptor antagonists, 4-(2-[7-amino-2-{2-furyl}{1,2,4}-triazolo{2,3a}{1,3,5}triazin-5-yl-amino]ethyl)phenol (ZM 241385, 20 nM) and 5-amino-7-(2-phenylethyl)-2-(2-furyl)-pyrazolo-[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine (SCH 58261, 20 nM), but not by the adenosine A1 receptor antagonist, 1,3-dipropyl-8-cyclopentylxanthine (DPCPX, 20 nM). Adenosine A2A receptors may activate adenylate cyclase and protein kinase A since CGS 21680 (10 nM) facilitation of [3H]acetylcholine release was occluded by 8-bromo-cAMP (0.5 mM) and forskolin (10 [mu]M) and prevented by H-89 (1 [mu]M), but unaffected by phorbol-12,13-didecanoate (250 nM) or bisindolylmaleimide I (1 [mu]M). The existence of adenosine A2A receptors in hippocampal nerve terminals was further confirmed by a Western blot immunoreactivity qualitatively identical to that found in the striatum. This constitutes the first pharmacological identification of canonical adenosine A2A receptors coupling to the expected cAMP/protein kinase A pathway in the hippocampus with the expected immunoreactivity. |
publishDate |
2002 |
dc.date.none.fl_str_mv |
2002 |
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/10316/4819 http://hdl.handle.net/10316/4819 https://doi.org/10.1016/S0014-2999(02)02475-5 |
url |
http://hdl.handle.net/10316/4819 https://doi.org/10.1016/S0014-2999(02)02475-5 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
European Journal of Pharmacology. 454:1 (2002) 31-38 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
aplication/PDF |
dc.source.none.fl_str_mv |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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