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Diabetes downregulates renal adenosine A(2A) receptors in an experimental model of hypertension

Studies on diabetic nephropathy rarely take into account that the co-existence of diabetes and hypertension is frequent and further aggravates the prognosis of renal dysfunction. Adenosine can activate four subtypes of adenosine receptors (A(1), A(2A), A(2B) and A(3)) and has been implicated in diab...

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Autores principales: Patinha, Daniela, Carvalho, Carla, Abreu, Carla, Cunha, Olga M., Mota, Mariana C., Afonso, Joana, Albino-Teixeira, António, Diniz, Carmen, Morato, Manuela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544351/
https://www.ncbi.nlm.nih.gov/pubmed/31150459
http://dx.doi.org/10.1371/journal.pone.0217552
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author Patinha, Daniela
Carvalho, Carla
Abreu, Carla
Cunha, Olga M.
Mota, Mariana C.
Afonso, Joana
Albino-Teixeira, António
Diniz, Carmen
Morato, Manuela
author_facet Patinha, Daniela
Carvalho, Carla
Abreu, Carla
Cunha, Olga M.
Mota, Mariana C.
Afonso, Joana
Albino-Teixeira, António
Diniz, Carmen
Morato, Manuela
author_sort Patinha, Daniela
collection PubMed
description Studies on diabetic nephropathy rarely take into account that the co-existence of diabetes and hypertension is frequent and further aggravates the prognosis of renal dysfunction. Adenosine can activate four subtypes of adenosine receptors (A(1), A(2A), A(2B) and A(3)) and has been implicated in diabetic nephropathy. However, it is not known if, in hypertensive conditions, diabetes alters the presence/distribution profile of renal adenosine receptors. The aim of this work was to describe the presence/distribution profile of the four adenosine receptors in six renal structures (superficial/deep glomeruli, proximal/distal tubules, loop of Henle, collecting tubule) of the hypertensive kidney and to evaluate whether it is altered by diabetes. Immunoreactivities against the adenosine receptors were analyzed in six renal structures from spontaneously hypertensive rats (SHR, the control group) and from SHR rats with diabetes induced by streptozotocyin (SHR-STZ group). Data showed, for the first time, that all adenosine receptors were present in the kidney of SHR rats, although the distribution pattern was specific for each adenosine receptor subtype. Also, induction of diabetes in the SHR was associated with downregulation of adenosine A(2A) receptors, which might be relevant for the development of hypertensive diabetic nephropathy. This study highlights the adenosine A(2A) receptors as a potential target to explore to prevent and/or treat early diabetes-induced hyperfiltration, at least in hypertensive conditions.
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spelling pubmed-65443512019-06-17 Diabetes downregulates renal adenosine A(2A) receptors in an experimental model of hypertension Patinha, Daniela Carvalho, Carla Abreu, Carla Cunha, Olga M. Mota, Mariana C. Afonso, Joana Albino-Teixeira, António Diniz, Carmen Morato, Manuela PLoS One Research Article Studies on diabetic nephropathy rarely take into account that the co-existence of diabetes and hypertension is frequent and further aggravates the prognosis of renal dysfunction. Adenosine can activate four subtypes of adenosine receptors (A(1), A(2A), A(2B) and A(3)) and has been implicated in diabetic nephropathy. However, it is not known if, in hypertensive conditions, diabetes alters the presence/distribution profile of renal adenosine receptors. The aim of this work was to describe the presence/distribution profile of the four adenosine receptors in six renal structures (superficial/deep glomeruli, proximal/distal tubules, loop of Henle, collecting tubule) of the hypertensive kidney and to evaluate whether it is altered by diabetes. Immunoreactivities against the adenosine receptors were analyzed in six renal structures from spontaneously hypertensive rats (SHR, the control group) and from SHR rats with diabetes induced by streptozotocyin (SHR-STZ group). Data showed, for the first time, that all adenosine receptors were present in the kidney of SHR rats, although the distribution pattern was specific for each adenosine receptor subtype. Also, induction of diabetes in the SHR was associated with downregulation of adenosine A(2A) receptors, which might be relevant for the development of hypertensive diabetic nephropathy. This study highlights the adenosine A(2A) receptors as a potential target to explore to prevent and/or treat early diabetes-induced hyperfiltration, at least in hypertensive conditions. Public Library of Science 2019-05-31 /pmc/articles/PMC6544351/ /pubmed/31150459 http://dx.doi.org/10.1371/journal.pone.0217552 Text en © 2019 Patinha et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Patinha, Daniela
Carvalho, Carla
Abreu, Carla
Cunha, Olga M.
Mota, Mariana C.
Afonso, Joana
Albino-Teixeira, António
Diniz, Carmen
Morato, Manuela
Diabetes downregulates renal adenosine A(2A) receptors in an experimental model of hypertension
title Diabetes downregulates renal adenosine A(2A) receptors in an experimental model of hypertension
title_full Diabetes downregulates renal adenosine A(2A) receptors in an experimental model of hypertension
title_fullStr Diabetes downregulates renal adenosine A(2A) receptors in an experimental model of hypertension
title_full_unstemmed Diabetes downregulates renal adenosine A(2A) receptors in an experimental model of hypertension
title_short Diabetes downregulates renal adenosine A(2A) receptors in an experimental model of hypertension
title_sort diabetes downregulates renal adenosine a(2a) receptors in an experimental model of hypertension
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544351/
https://www.ncbi.nlm.nih.gov/pubmed/31150459
http://dx.doi.org/10.1371/journal.pone.0217552
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