Cyclic nucleotide phosphodiesterases: molecular regulation to clinical use

AT Bender, JA Beavo - Pharmacological reviews, 2006 - ASPET
Cyclic nucleotide phosphodiesterases (PDEs) are enzymes that regulate the cellular levels
of the second messengers, cAMP and cGMP, by controlling their rates of degradation. There …

Cyclic nucleotide phosphodiesterase (PDE) isozymes as targets of the intracellular signalling network: benefits of PDE inhibitors in various diseases and perspectives …

T Keravis, C Lugnier - British journal of pharmacology, 2012 - Wiley Online Library
Cyclic nucleotide phosphodiesterases (PDEs) that specifically inactivate the intracellular
messengers cAMP and cGMP in a compartmentalized manner represent an important …

Cyclic nucleotide phosphodiesterase (PDE) superfamily: a new target for the development of specific therapeutic agents

C Lugnier - Pharmacology & therapeutics, 2006 - Elsevier
Cyclic nucleotide phosphodiesterases (PDEs), which are ubiquitously distributed in
mammalian tissues, play a major role in cell signaling by hydrolyzing cAMP and cGMP. Due …

Clinical and molecular genetics of the phosphodiesterases (PDEs)

MF Azevedo, FR Faucz, E Bimpaki, A Horvath… - Endocrine …, 2014 - academic.oup.com
Cyclic nucleotide phosphodiesterases (PDEs) are enzymes that have the unique function of
terminating cyclic nucleotide signaling by catalyzing the hydrolysis of cAMP and GMP. They …

Selective phosphodiesterase inhibitors: a promising target for cognition enhancement

OAH Reneerkens, K Rutten, HWM Steinbusch… - …, 2009 - Springer
Rationale One of the major complaints most people face during aging is an impairment in
cognitive functioning. This has a negative impact on the quality of daily life and is even more …

Phosphodiesterase inhibitors say NO to Alzheimer's disease

SM Nabavi, S Talarek, J Listos, SF Nabavi… - Food and Chemical …, 2019 - Elsevier
Phosphodiesterases (PDEs) consisted of 11 subtypes (PDE1 to PDE11) and over 40
isoforms that regulate levels of cyclic guanosine monophosphate (cGMP) and cyclic …

Phosphodiesterase 8 governs cAMP/PKA-dependent reduction of L-type calcium current in human atrial fibrillation: a novel arrhythmogenic mechanism

N Grammatika Pavlidou, S Dobrev… - European heart …, 2023 - academic.oup.com
Aims Atrial fibrillation (AF) is associated with altered cAMP/PKA signaling and an AF-
promoting reduction of L-type Ca2+-current (ICa, L), the mechanisms of which are poorly …

[HTML][HTML] Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function

L Arnaud-Lopez, G Usala, G Ceresini… - The American Journal of …, 2008 - cell.com
Thyroid-stimulating hormone (TSH) controls thyroid growth and hormone secretion through
binding to its G protein-coupled receptor (TSHR) and production of cyclic AMP (cAMP) …

cAMP-specific phosphodiesterase inhibitors: promising drugs for inflammatory and neurological diseases

A Martinez, C Gil - Expert opinion on therapeutic patents, 2014 - Taylor & Francis
Introduction: PDEs are key enzymes in the adenosine and guanosine cyclic nucleotides
(cAMP and cGMP) signaling cascade. Their inhibition increases cyclic nucleotide levels …

[图书][B] Cyclic nucleotide phosphodiesterases in health and disease

J Beavo, SH Francis, MD Houslay - 2007 - api.taylorfrancis.com
The establishment of a Gordon Research Conference devoted to cyclic nucleotide
phosphodiesterases has had an enormous impact on the field by facilitating collaborations …