Results 11 to 20 of about 4,135 (194)

Evaluation of the acute oral toxicity and antipsychotic activity of a dual inhibitor of PDE1B and PDE10A in rat model of schizophrenia.

open access: goldPLoS ONE, 2022
Phosphodiesterase 1B (PDE1B) and PDE10A are dual-specificity PDEs that hydrolyse both cyclic adenosine monophosphate and cyclic guanosine monophosphate, and are highly expressed in the striatum.
Mayasah Al-Nema   +5 more
doaj   +4 more sources

Integrative multi-omics analyses identify key genes and elucidate bidirectional regulatory mechanisms in thyroid dysfunction. [PDF]

open access: yesPLoS ONE
ObjectiveHyperthyroidism and hypothyroidism are globally prevalent endocrine disorders, with their pathogenesis involving multifactorial mechanisms including genetics, immunity, and metabolism.
Yilang Hu   +8 more
doaj   +2 more sources

A Novel PDE10A Inhibitor for Tourette Syndrome and Other Movement Disorders [PDF]

open access: yesCells
Background: Tourette syndrome is a neurodevelopmental movement disorder involving basal ganglia dysfunction. PDE10A inhibitors modulate signaling in the striatal basal ganglia nuclei and are thus of interest as potential therapeutics in treating Tourette
Randall D. Marshall   +2 more
doaj   +2 more sources

In Silico study of PDE10A inhibitors for schizophrenia: molecular docking, ADMET and DFT analysis [PDF]

open access: diamondDiscover Chemistry
Recently, interest in phosphodiesterase 10 A inhibitors has increased for schizophrenia treatment. Medicinal chemists have extensively worked on developing potent PDE10A inhibitors with minimal side effects.
Ashutosh Kharwar   +2 more
doaj   +2 more sources

Effects of the Phosphodiesterase 10A Inhibitor MR1916 on Alcohol Self-Administration and Striatal Gene Expression in Post-Chronic Intermittent Ethanol-Exposed Rats [PDF]

open access: yesCells
Alcohol use disorder (AUD) requires new neurobiological targets. Problematic drinking involves underactive indirect pathway medium spiny neurons (iMSNs) that subserve adaptive behavioral selection vs.
Luísa B. Bertotto   +5 more
doaj   +2 more sources

Papaverine, a phosphodiesterase 10A inhibitor, ameliorates quinolinic acid-induced synaptotoxicity in human cortical neurons [PDF]

open access: yes, 2021
Phosphodiesterase-10A (PDE10A) hydrolyse the secondary messengers cGMP and cAMP, two molecules playing important roles in neurodevelopment and brain functions.
Basappa, S.   +7 more
core   +1 more source

Early-Onset Movement Disorder Syndrome Caused by Biallelic Variants in PDE1B Encoding Phosphodiesterase 1B. [PDF]

open access: yesMov Disord
Abstract Background Breakdown of cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP) in basal ganglia cells through hydrolysis of diesteric bonds, primarily by PDE10A and PDE1B, is essential for normal human movement. While biallelic loss‐of‐function variants in PDE10A are known to cause hyperkinetic movement disorders, the ...
Poleg T   +21 more
europepmc   +2 more sources

PDE10A Inhibitors—Clinical Failure or Window Into Antipsychotic Drug Action?

open access: yesFrontiers in Neuroscience, 2021
PDE10A, a phosphodiesterase that inactivates both cAMP and cGMP, is a unique signaling molecule in being highly and nearly exclusively expressed in striatal medium spiny neurons.
Frank S. Menniti   +2 more
doaj   +1 more source

Discovery of a highly specific 18F-labeled PET ligand for phosphodiesterase 10A enabled by novel spirocyclic iodonium ylide radiofluorination

open access: yesActa Pharmaceutica Sinica B, 2022
As a member of cyclic nucleotide phosphodiesterase (PDE) enzyme family, PDE10A is in charge of the degradation of cyclic adenosine (cAMP) and guanosine monophosphates (cGMP). While PDE10A is primarily expressed in the medium spiny neurons of the striatum,
Zhiwei Xiao   +21 more
doaj   +1 more source

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