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- W1987383838 endingPage "411" @default.
- W1987383838 startingPage "395" @default.
- W1987383838 abstract "Background: Nicotinic acetylcholine receptors (nAChRs) are ligand-gated ion channels that participate in many physiological functions. Receptors result from the assembly of five homologous or heterologous subunits that form the ligand-binding site and an ionic pore. In vertebrates, 17 subunits have been identified, α (1 – 10), β (1 – 4), γ, δ and ϵ. Assembly of different subunit combinations allows a diversity of physiological and pharmacological properties. Objective: To review the putative involvement of nAChRs in several diseases. Methods: We discuss the expression pattern of the subunits, the pharmacological tools for distinguishing them and their role in pathogenesis. Results/conclusion: Long-standing efforts in this field should soon result in the finding of new molecules that might be applicable to situations ranging from neurological diseases to immune treatments." @default.
- W1987383838 created "2016-06-24" @default.
- W1987383838 creator A5034835507 @default.
- W1987383838 creator A5063992837 @default.
- W1987383838 date "2009-03-31" @default.
- W1987383838 modified "2023-10-03" @default.
- W1987383838 title "Nicotinic acetylcholine receptors: an overview on drug discovery" @default.
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