Atypical antipsychotics as noncompetitive inhibitors of alpha 4 beta 2 and alpha 7 neuronal nicotinic receptors

作者：Grinevich Vladimir P; Papke Roger L; Lippiello Patrick M; Bencherif Merouane^*

来源：Neuropharmacology, 2009, 57(2): 183-191.

DOI：10.1016/j.neuropharm.2009.05.003

• Antipsychotics
• Nicotinic receptors
• Cholinergic
• Schizophrenia

It has been suggested that the interaction of antipsychotic medications with neuronal nicotinic receptors may increase the cognitive dysfunction associated with schizophrenia and may explain why current therapies only partially address this core feature of the illness. In the present studies we compared the effects of the atypical antipsychotics quetiapine, clozapine and N-desmethylclozapine to those of the typical antipsychotics haloperidol and chlorpromazine on the alpha 4 beta 2 and alpha 7 nicotinic receptor subtypes. The binding of [(3)H]-nicotine to rat cortical alpha A beta 2 receptors and [(3)H]-methyllycaconitine to rat hippocampal alpha 7 receptors was not affected by any of the compounds tested. However, Rb( ) efflux evoked either by nicotine or the selective alpha 4 beta 2 agonist TC-1827 from alpha 4 beta 2 receptors expressed in SH-EP1 cells and nicotine-evoked [(3)H]-dopamine release from rat striatal synaptosomes were non-competitively inhibited by all of the antipsychotics. Similarly, alpha-bungarotoxin-sensitive epibatidine-evoked [(3)H]-norepinephrine release from rat hippocampal slices and acetylcholine-activated currents of alpha 7 nicotinic receptors expressed in oocytes were inhibited by haloperidol, chlorpromazine, clozapine and N-desmethylclozapine. The inhibitory effects on nicotinic receptor function produced by the antipsychotics tested occurred at concentrations similar to plasma levels achieved in schizophrenia patients, suggesting that they may lead to clinically relevant effects on cognition.

• 出版日期2009-8