Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8350697 | Pharmacology Biochemistry and Behavior | 2015 | 11 Pages |
Abstract
Novel pharmacological treatments targeting alpha 7 nicotinic acetylcholine receptor (α7 nAChR) hypofunction in schizophrenia have shown mixed success in ameliorating cognitive impairments associated with this disorder. Choline, a selective agonist at α7 receptors is increased with oral administration of cytidine 5â²-diphosphocholine (CDP-choline), the cognitive effects of which were assessed in healthy volunteers. Using the CogState test battery, behavioral performance in schizophrenia-relevant cognitive domains was assessed in 24 male participants following a single low (500 mg) and moderate (1000 mg) dose of CDP-choline. Relative to placebo, CDP-choline improved processing speed, working memory, verbal learning, verbal memory, and executive function in low baseline performers, while exerting no effects in medium baseline performers, and diminishing cognition in high baseline performers. Dose effects varied with cognitive domain but were evident with both the 500 mg and 1000 mg doses. These preliminary findings of cognitive enhancement in relatively impaired performers are consistent with the α7 receptor mechanism and support further trials with CDP-choline as a potential pro-cognitive strategy for cognitive impairment in schizophrenia.
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Authors
Verner Knott, Sara de la Salle, Joelle Choueiry, Danielle Impey, Dylan Smith, Meaghan Smith, Elise Beaudry, Salman Saghir, Vadim Ilivitsky, Alain Labelle,