Muscarinic acetylcholine receptor subtypes have been the subjects of resear
ch for at least a quarter of a century. Nonetheless, there are few selectiv
e muscarinic receptor ligands presently used as therapeutics. The extensive
development of muscarinic Mi receptor agonists for the treatment of cognit
ive dysfunction has culminated in a series of unsuccessful drug candidates,
which reflects a lack of understanding of the disease and the role played
by muscarinic cholinergic transmission. Paradoxically, the most successful
antagonist approved for use in urinary incontinence is the nonselective mus
carinic receptor antagonist tolterodine. This deficit in subtype-selective
ligands could be circumvented by the development of transgenic mice, each l
acking functional M-1, M-2, M-3, M-4 or M-5 receptors. In this article, the
current status of muscarinic receptor research is critically assessed.