Skip to Content
by Leigh MacMillan | Posted on Tuesday, Jul. 17, 2012 — 7:00 AM
Drugs that selectively activate the “M1” type of muscarinic acetylcholine receptor are being explored as new treatments for schizophrenia and other major brain disorders.
Jeffrey Conn, Lee E. Limbird Chair in Pharmacology, and colleagues have discovered novel M1 allosteric agonists, drugs that can “turn up” the activity of the M1 receptor. They now report that two of these compounds activate some – but not all – M1-regulated signaling pathways in cells. They further demonstrate that these drugs have robust effects in some brain areas, such as the hippocampus, but not in other brain regions, and that these differences correspond to behavioral effects in animal models. Both M1 agonists enhanced hippocampal-dependent cognitive functions, but did not exhibit antipsychotic activity in rats.
The studies in the June 20 Journal of Neuroscience offer new insights for M1 receptor-mediated responses and drug development. They emphasize the importance of measuring drug effects on multiple cellular signaling pathways and in multiple brain systems to avoid advancing drug candidates that have restricted physiological effects.
This research was supported by grants from the National Institute of Mental Health (MH084659, MH082867, MH087965, MH073676, MH087039, MH065215) and the National Institute of Neurological Disorders and Stroke (NS071746, NS065867) of the National Institutes of Health.
Send suggestions for research to highlight in Aliquots to: firstname.lastname@example.org
Leigh MacMillan, (615) 322-4747
Health and Medicine, Reporter, Research acetylcholine, Aliquots, Allosteric modulator, brain, chemistry, drug discovery, Jeffrey Conn, Journal of Neuroscience, journal publication, NIH, NIMH, NINDS, pharmacology, psychosis, Reporter July 13 2012, schizophrenia, Vanderbilt Center for Neuroscience Drug Discovery
There are lots of ways to keep up with Vanderbilt. Choose your preferred method: