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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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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. |
format | Online Article Text |
id | pubmed-6544351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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