Modulation of compartmentalized cyclic nucleotide signalling via local inhibition of phosphodiesterase activity

Cyclic nucleotides phosphodiesterases (PDEs) are the only enzymes that degrade the cyclic nucleotides cAMP and cGMP and play a key role in modulating the amplitude and duration of the signal delivered by these two key intracellular second messengers. Defects in cyclic nucleotide signalling are kn...

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Main Authors: Brescia, M, Zaccolo, M
Format: Journal article
Published: MDPI 2016
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author Brescia, M
Zaccolo, M
author_facet Brescia, M
Zaccolo, M
author_sort Brescia, M
collection OXFORD
description Cyclic nucleotides phosphodiesterases (PDEs) are the only enzymes that degrade the cyclic nucleotides cAMP and cGMP and play a key role in modulating the amplitude and duration of the signal delivered by these two key intracellular second messengers. Defects in cyclic nucleotide signalling are known to be involved in several pathologies. As a consequence, PDEs have been long recognized as potential drug targets, and they have been the focus of intense research for the development of therapeutic agents. A number of PDE inhibitors are currently available for the treatment of disease, including obstructive pulmonary disease, erectile dysfunction and heart failure. However, the performance of these drugs is not always satisfactory due to lack of PDE-isoform specificity and their consequent adverse side effects. Recent advances in our understanding of compartmentalized cyclic nucleotide signalling and the role of PDEs in local regulation of cAMP and cGMP signals offers the opportunity for the development of novel strategies for therapeutic intervention that may overcome the current limitation of conventional PDE inhibitors.
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spelling oxford-uuid:03cd9c75-6242-4d3a-9b2d-e0af64f0290b2022-03-26T08:48:20ZModulation of compartmentalized cyclic nucleotide signalling via local inhibition of phosphodiesterase activityJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:03cd9c75-6242-4d3a-9b2d-e0af64f0290bSymplectic Elements at OxfordMDPI2016Brescia, MZaccolo, MCyclic nucleotides phosphodiesterases (PDEs) are the only enzymes that degrade the cyclic nucleotides cAMP and cGMP and play a key role in modulating the amplitude and duration of the signal delivered by these two key intracellular second messengers. Defects in cyclic nucleotide signalling are known to be involved in several pathologies. As a consequence, PDEs have been long recognized as potential drug targets, and they have been the focus of intense research for the development of therapeutic agents. A number of PDE inhibitors are currently available for the treatment of disease, including obstructive pulmonary disease, erectile dysfunction and heart failure. However, the performance of these drugs is not always satisfactory due to lack of PDE-isoform specificity and their consequent adverse side effects. Recent advances in our understanding of compartmentalized cyclic nucleotide signalling and the role of PDEs in local regulation of cAMP and cGMP signals offers the opportunity for the development of novel strategies for therapeutic intervention that may overcome the current limitation of conventional PDE inhibitors.
spellingShingle Brescia, M
Zaccolo, M
Modulation of compartmentalized cyclic nucleotide signalling via local inhibition of phosphodiesterase activity
title Modulation of compartmentalized cyclic nucleotide signalling via local inhibition of phosphodiesterase activity
title_full Modulation of compartmentalized cyclic nucleotide signalling via local inhibition of phosphodiesterase activity
title_fullStr Modulation of compartmentalized cyclic nucleotide signalling via local inhibition of phosphodiesterase activity
title_full_unstemmed Modulation of compartmentalized cyclic nucleotide signalling via local inhibition of phosphodiesterase activity
title_short Modulation of compartmentalized cyclic nucleotide signalling via local inhibition of phosphodiesterase activity
title_sort modulation of compartmentalized cyclic nucleotide signalling via local inhibition of phosphodiesterase activity
work_keys_str_mv AT bresciam modulationofcompartmentalizedcyclicnucleotidesignallingvialocalinhibitionofphosphodiesteraseactivity
AT zaccolom modulationofcompartmentalizedcyclicnucleotidesignallingvialocalinhibitionofphosphodiesteraseactivity