Combining CDP-choline and galantamine: Effects of a selective α7 nicotinic acetylcholine receptor agonist strategy on P50 sensory gating of speech sounds in healthy volunteers.


Journal

Journal of psychopharmacology (Oxford, England)
ISSN: 1461-7285
Titre abrégé: J Psychopharmacol
Pays: United States
ID NLM: 8907828

Informations de publication

Date de publication:
06 2019
Historique:
pubmed: 29 3 2019
medline: 24 6 2020
entrez: 29 3 2019
Statut: ppublish

Résumé

Schizophrenia (SCZ) patients and relatives have deficits in early cortical sensory gating (SG) typically measured by suppression of electroencephalography-derived P50 event-related potentials (ERPs) in a conditioning-testing (S This pilot study in healthy humans assessed the SG effects of an α7 nAChR strategy combining CDP-choline with galantamine, a positive allosteric modulator (PAM) of nAChRs, aimed at increasing and prolonging nicotinic receptor activity. The combined effect of CDP-choline (500 mg) and galantamine (16 mg) on speech P50 gating indices rP50 (S In low suppressors, CDP-choline/galantamine (vs. placebo) improved rP50 and dP50 gating, and reduced S Findings from this pilot study with CDP-choline/galantamine in a healthy, SCZ-like surrogate deficient gating sample are consistent with the association of α7 nAChR mechanisms in SG impairment in SCZ and support further research trials with CDP-choline and galantamine targeting sensory processes.

Sections du résumé

BACKGROUND
Schizophrenia (SCZ) patients and relatives have deficits in early cortical sensory gating (SG) typically measured by suppression of electroencephalography-derived P50 event-related potentials (ERPs) in a conditioning-testing (S
AIMS
This pilot study in healthy humans assessed the SG effects of an α7 nAChR strategy combining CDP-choline with galantamine, a positive allosteric modulator (PAM) of nAChRs, aimed at increasing and prolonging nicotinic receptor activity.
METHODS
The combined effect of CDP-choline (500 mg) and galantamine (16 mg) on speech P50 gating indices rP50 (S
RESULTS
In low suppressors, CDP-choline/galantamine (vs. placebo) improved rP50 and dP50 gating, and reduced S
CONCLUSION
Findings from this pilot study with CDP-choline/galantamine in a healthy, SCZ-like surrogate deficient gating sample are consistent with the association of α7 nAChR mechanisms in SG impairment in SCZ and support further research trials with CDP-choline and galantamine targeting sensory processes.

Identifiants

pubmed: 30920339
doi: 10.1177/0269881119836217
doi:

Substances chimiques

Nicotinic Agonists 0
Nootropic Agents 0
Receptors, Nicotinic 0
alpha7 Nicotinic Acetylcholine Receptor 0
Galantamine 0D3Q044KCA
Cytidine Diphosphate Choline 536BQ2JVC7
Nicotine 6M3C89ZY6R

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

688-699

Subventions

Organisme : CIHR
Pays : Canada

Auteurs

Joelle Choueiry (J)

1 Department of Neuroscience, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.

Crystal M Blais (CM)

2 Institute of Cognitive Science, Carleton University, Ottawa, ON, Canada.

Dhrasti Shah (D)

3 School of Psychology, Faculty of Social Sciences, University of Ottawa, Ottawa, ON, Canada.

Dylan Smith (D)

3 School of Psychology, Faculty of Social Sciences, University of Ottawa, Ottawa, ON, Canada.

Derek Fisher (D)

4 Department of Psychology, Faculty of Social Sciences, Mount Saint Vincent University, Halifax, NS, Canada.

Vadim Illivitsky (V)

5 The Royal Ottawa Mental Health Centre, Ottawa, ON, Canada.

Verner Knott (V)

1 Department of Neuroscience, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.
2 Institute of Cognitive Science, Carleton University, Ottawa, ON, Canada.
3 School of Psychology, Faculty of Social Sciences, University of Ottawa, Ottawa, ON, Canada.
5 The Royal Ottawa Mental Health Centre, Ottawa, ON, Canada.
6 University of Ottawa Institute of Mental Health Research, Ottawa, ON, Canada.

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Classifications MeSH