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The Guanine-Based Purinergic System: The Tale of An Orphan Neuromodulation

Guanine-based purines (GBPs) have been recently proposed to be not only metabolic agents but also extracellular signaling molecules that regulate important functions in the central nervous system. In such way, GBPs-mediated neuroprotection, behavioral responses and neuronal plasticity have been broa...

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Autores principales: Di Liberto, Valentina, Mudò, Giuseppa, Garozzo, Roberta, Frinchi, Monica, Fernandez-Dueñas, Víctor, Di Iorio, Patrizia, Ciccarelli, Renata, Caciagli, Francesco, Condorelli, Daniele F., Ciruela, Francisco, Belluardo, Natale
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4911385/
https://www.ncbi.nlm.nih.gov/pubmed/27378923
http://dx.doi.org/10.3389/fphar.2016.00158
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author Di Liberto, Valentina
Mudò, Giuseppa
Garozzo, Roberta
Frinchi, Monica
Fernandez-Dueñas, Víctor
Di Iorio, Patrizia
Ciccarelli, Renata
Caciagli, Francesco
Condorelli, Daniele F.
Ciruela, Francisco
Belluardo, Natale
author_facet Di Liberto, Valentina
Mudò, Giuseppa
Garozzo, Roberta
Frinchi, Monica
Fernandez-Dueñas, Víctor
Di Iorio, Patrizia
Ciccarelli, Renata
Caciagli, Francesco
Condorelli, Daniele F.
Ciruela, Francisco
Belluardo, Natale
author_sort Di Liberto, Valentina
collection PubMed
description Guanine-based purines (GBPs) have been recently proposed to be not only metabolic agents but also extracellular signaling molecules that regulate important functions in the central nervous system. In such way, GBPs-mediated neuroprotection, behavioral responses and neuronal plasticity have been broadly described in the literature. However, while a number of these functions (i.e., GBPs neurothophic effects) have been well-established, the molecular mechanisms behind these GBPs-dependent effects are still unknown. Furthermore, no plasma membrane receptors for GBPs have been described so far, thus GBPs are still considered orphan neuromodulators. Interestingly, an intricate and controversial functional interplay between GBPs effects and adenosine receptors activity has been recently described, thus triggering the hypothesis that GBPs mechanism of action might somehow involve adenosine receptors. Here, we review recent data describing the GBPs role in the brain. We focus on the involvement of GBPs regulating neuronal plasticity, and on the new hypothesis based on putative GBPs receptors. Overall, we expect to shed some light on the GBPs world since although these molecules might represent excellent candidates for certain neurological diseases management, the lack of putative GBPs receptors precludes any high throughput screening intent for the search of effective GBPs-based drugs.
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spelling pubmed-49113852016-07-04 The Guanine-Based Purinergic System: The Tale of An Orphan Neuromodulation Di Liberto, Valentina Mudò, Giuseppa Garozzo, Roberta Frinchi, Monica Fernandez-Dueñas, Víctor Di Iorio, Patrizia Ciccarelli, Renata Caciagli, Francesco Condorelli, Daniele F. Ciruela, Francisco Belluardo, Natale Front Pharmacol Pharmacology Guanine-based purines (GBPs) have been recently proposed to be not only metabolic agents but also extracellular signaling molecules that regulate important functions in the central nervous system. In such way, GBPs-mediated neuroprotection, behavioral responses and neuronal plasticity have been broadly described in the literature. However, while a number of these functions (i.e., GBPs neurothophic effects) have been well-established, the molecular mechanisms behind these GBPs-dependent effects are still unknown. Furthermore, no plasma membrane receptors for GBPs have been described so far, thus GBPs are still considered orphan neuromodulators. Interestingly, an intricate and controversial functional interplay between GBPs effects and adenosine receptors activity has been recently described, thus triggering the hypothesis that GBPs mechanism of action might somehow involve adenosine receptors. Here, we review recent data describing the GBPs role in the brain. We focus on the involvement of GBPs regulating neuronal plasticity, and on the new hypothesis based on putative GBPs receptors. Overall, we expect to shed some light on the GBPs world since although these molecules might represent excellent candidates for certain neurological diseases management, the lack of putative GBPs receptors precludes any high throughput screening intent for the search of effective GBPs-based drugs. Frontiers Media S.A. 2016-06-17 /pmc/articles/PMC4911385/ /pubmed/27378923 http://dx.doi.org/10.3389/fphar.2016.00158 Text en Copyright © 2016 Di Liberto, Mudò, Garozzo, Frinchi, Fernández-Dueñas, Di Iorio, Ciccarelli, Caciagli, Condorelli, Ciruela and Belluardo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Di Liberto, Valentina
Mudò, Giuseppa
Garozzo, Roberta
Frinchi, Monica
Fernandez-Dueñas, Víctor
Di Iorio, Patrizia
Ciccarelli, Renata
Caciagli, Francesco
Condorelli, Daniele F.
Ciruela, Francisco
Belluardo, Natale
The Guanine-Based Purinergic System: The Tale of An Orphan Neuromodulation
title The Guanine-Based Purinergic System: The Tale of An Orphan Neuromodulation
title_full The Guanine-Based Purinergic System: The Tale of An Orphan Neuromodulation
title_fullStr The Guanine-Based Purinergic System: The Tale of An Orphan Neuromodulation
title_full_unstemmed The Guanine-Based Purinergic System: The Tale of An Orphan Neuromodulation
title_short The Guanine-Based Purinergic System: The Tale of An Orphan Neuromodulation
title_sort guanine-based purinergic system: the tale of an orphan neuromodulation
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4911385/
https://www.ncbi.nlm.nih.gov/pubmed/27378923
http://dx.doi.org/10.3389/fphar.2016.00158
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