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Nuclear Factor κB and Adenosine Receptors: Biochemical and Behavioral Profiling
Adenosine is produced primarily by the metabolism of ATP and mediates its physiological actions by interacting primarily with adenosine receptors (ARs) on the plasma membranes of different cell types in the body. Activation of these G protein-coupled receptors promotes activation of diverse cellular...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Science Publishers Ltd
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3131724/ https://www.ncbi.nlm.nih.gov/pubmed/22131942 http://dx.doi.org/10.2174/157015911795596559 |
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author | Ramkumar, Vickram Jhaveri, Krishna A Xie, Xiaobin Jajoo, Sarvesh Toth, Linda A |
author_facet | Ramkumar, Vickram Jhaveri, Krishna A Xie, Xiaobin Jajoo, Sarvesh Toth, Linda A |
author_sort | Ramkumar, Vickram |
collection | PubMed |
description | Adenosine is produced primarily by the metabolism of ATP and mediates its physiological actions by interacting primarily with adenosine receptors (ARs) on the plasma membranes of different cell types in the body. Activation of these G protein-coupled receptors promotes activation of diverse cellular signaling pathways that define their tissue-specific functions. One of the major actions of adenosine is cytoprotection, mediated primarily via two ARs - A(1) (A(1)AR) and A(3) (A(3)AR). These ARs protect cells exposed to oxidative stress and are also regulated by oxidative stress. Stress-mediated regulation of ARs involves two prominent transcription factors - activator protein-1 (AP-1) and nuclear factor (NF)-κB – that mediate the induction of genes important in cell survival. Mice that are genetically deficient in the p50 subunit of NF-κB (i.e., p50 knock-out mice) exhibit altered expression of A(1)AR and A(2A)AR and demonstrate distinct behavioral phenotypes under normal conditions or after drug challenges. These effects suggest an important role for NF-κB in dictating the level of expression of ARs in vivo, in regulating the cellular responses to stress, and in modifying behavior. |
format | Online Article Text |
id | pubmed-3131724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Bentham Science Publishers Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-31317242011-12-01 Nuclear Factor κB and Adenosine Receptors: Biochemical and Behavioral Profiling Ramkumar, Vickram Jhaveri, Krishna A Xie, Xiaobin Jajoo, Sarvesh Toth, Linda A Curr Neuropharmacol Article Adenosine is produced primarily by the metabolism of ATP and mediates its physiological actions by interacting primarily with adenosine receptors (ARs) on the plasma membranes of different cell types in the body. Activation of these G protein-coupled receptors promotes activation of diverse cellular signaling pathways that define their tissue-specific functions. One of the major actions of adenosine is cytoprotection, mediated primarily via two ARs - A(1) (A(1)AR) and A(3) (A(3)AR). These ARs protect cells exposed to oxidative stress and are also regulated by oxidative stress. Stress-mediated regulation of ARs involves two prominent transcription factors - activator protein-1 (AP-1) and nuclear factor (NF)-κB – that mediate the induction of genes important in cell survival. Mice that are genetically deficient in the p50 subunit of NF-κB (i.e., p50 knock-out mice) exhibit altered expression of A(1)AR and A(2A)AR and demonstrate distinct behavioral phenotypes under normal conditions or after drug challenges. These effects suggest an important role for NF-κB in dictating the level of expression of ARs in vivo, in regulating the cellular responses to stress, and in modifying behavior. Bentham Science Publishers Ltd 2011-06 /pmc/articles/PMC3131724/ /pubmed/22131942 http://dx.doi.org/10.2174/157015911795596559 Text en ©2011 Bentham Science Publishers Ltd. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestrictive use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Ramkumar, Vickram Jhaveri, Krishna A Xie, Xiaobin Jajoo, Sarvesh Toth, Linda A Nuclear Factor κB and Adenosine Receptors: Biochemical and Behavioral Profiling |
title | Nuclear Factor κB and Adenosine Receptors: Biochemical and Behavioral Profiling |
title_full | Nuclear Factor κB and Adenosine Receptors: Biochemical and Behavioral Profiling |
title_fullStr | Nuclear Factor κB and Adenosine Receptors: Biochemical and Behavioral Profiling |
title_full_unstemmed | Nuclear Factor κB and Adenosine Receptors: Biochemical and Behavioral Profiling |
title_short | Nuclear Factor κB and Adenosine Receptors: Biochemical and Behavioral Profiling |
title_sort | nuclear factor κb and adenosine receptors: biochemical and behavioral profiling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3131724/ https://www.ncbi.nlm.nih.gov/pubmed/22131942 http://dx.doi.org/10.2174/157015911795596559 |
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