Nootropic drug modulation of neuronal nicotinic acetylcholine receptors inrat cortical neurons

Nefiracetam (DM-9384) is a new pyrrolidone nootropic drug being developed f or the treatment of Alzheimer's type and poststroke vascular-type dementia. Because the cholinergic system plays an important role in cognitive functi ons and Alzheimer's disease dementia, the present study was conducted to el ucidate the mechanism of action of nefiracetam and aniracetam on neuronal n icotinic acetylcholine receptors (nnAChRs). Currents were recorded from rat cortical neurons in long-term primary culture using the whole-cell, patch- clamp technique. Two types of currents were evoked by acetylcholine (ACh): alpha -bungarotoxin-sensitive, alpha7-type currents and alpha -bungarotoxin -insensitive, alpha4 beta2-type currents. Although nefiracetam and aniracet am inhibited alpha7-type currents only weakly, these nootropic agents poten tiated alpha4 beta2-type currents in a very potent and efficacious manner. Nefiracetam at 1 nM and aniracetam at 0.1 nM reversibly potentiated alpha4 beta2-type currents to 200 to 300% of control. Nefiracetam at very high con centrations (similar to 10 muM) also potentiated alpha4 beta2-type currents but to a lesser extent, indicative of a bell-shaped dose-response relation ship. Nefiracetam markedly increased the saturating responses induced by hi gh concentrations of ACh. However, human alpha4 beta2 subunits expressed in human embryonic kidney cells were inhibited rather than potentiated by nef iracetam. The specific protein kinase A inhibitors (H-89, KT5720, and pepti de 5-24) and protein kinase C inhibitors (chelerythrine, calphostin C, and peptide 19-63) did not prevent nefiracetam from potentiating a4b2-type curr ents, indicating that these protein kinases are not involved in nefiracetam action. The nefiracetam potentiating action was not affected by 24-h pretr eatment of neurons with pertussis toxin, but was abolished by cholera toxin . Therefore, G(s) proteins, but not G(i)/G(o) proteins, are involved in nef iracetam potentiation. These results indicate that nnAChRs are an important site of action of nefiracetam and G(s) proteins may be its crucial target.