Abstract
The regionally selective reduction of expression of the α7 nicotinic acetylcholine receptor (α7 nAChR) in schizophrenia underlies impaired sensory inhibition, a possible endophenotype of the disorder. This ligand-gated ion channel receptor has been proposed as a pharmacotherapeutic target in schizophrenia. The current study examined the effect of CDP-choline alone and the combination of CDP-choline and galantamine, administered acutely and once-daily for five consecutive days, in an animal model of NMDA receptor hypofunction that is relevant to schizophrenia. The results support the allosteric modulatory influence of galantamine on CDP-choline; however, individual doses of CDP-choline and galantamine must be carefully titrated in order to achieve optimal levels of α7 nAChR "agonism" that may be necessary for the desired therapeutic effect.
| Original language | English |
|---|---|
| Pages (from-to) | 147-151 |
| Number of pages | 5 |
| Journal | European Neuropsychopharmacology |
| Volume | 18 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 2008 |
Keywords
- CDP-choline
- Galantamine
- NMDA receptor
- Schizophrenia
- α nicotinic acetylcholine receptor
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