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Characterization of a Novel M1Muscarinic Acetylcholine Receptor Positive Allosteric Modulator Radioligand, [3H]PT-1284
- Source :
- Molecular Pharmacology; 2016, Vol. 90 Issue: 3 p177-187, 11p
- Publication Year :
- 2016
-
Abstract
- Selective activation of the M1muscarinic acetylcholine receptor (mAChR) via a positive allosteric modulator (PAM) is a new approach for the treatment of the cognitive impairments associated with schizophrenia and Alzheimer’s disease. Herein, we describe the characterization of an M1PAM radioligand, 8-((1S,2S)-2-hydroxycyclohexyl)-5-((6-(methyl-t3)pyridin-3-yl)methyl)-8,9-dihydro-7H-pyrrolo[3,4-hour]quinolin-7-one ([3H]PT-1284), as a tool for characterizing the M1allosteric binding site, as well as profiling novel M1PAMs. 8-((1S,2S)-2-Hydroxycyclohexyl)-5-((6-methylpyridin-3-yl)methyl)-8,9-dihydro-7H-pyrrolo[3,4-hour]quinolin-7-one (PT-1284 (1)) was shown to potentiate acetylcholine (ACh) in an M1fluorometric imaging plate reader (FLIPR) functional assay (EC50, 36 nM) and carbachol in a hippocampal slice electrophysiology assay (EC50, 165 nM). PT-1284 (1) also reduced the concentration of ACh required to inhibit [3H]N-methylscopolamine ([3H]NMS) binding to M1, left-shifting the ACh Kiapproximately 19-fold at 10 μM. Saturation analysis of a human M1mAChR stable cell line showed that [3H]PT-1284 bound to M1mAChR in the presence of 1 mM ACh with Kd, 4.23 nM, and saturable binding capacity (Bmax), 6.38 pmol/mg protein. M1selective PAMs were shown to inhibit [3H]PT-1284 binding in a concentration-responsive manner, whereas M1allosteric and orthosteric agonists showed weak affinity (>30 μM). A strong positive correlation (R2= 0.86) was found to exist between affinity values generated for nineteen M1PAMs in the [3H]PT-1284 binding assay and the EC50values of these ligands in a FLIPR functional potentiation assay. These data indicate that there is a strong positive correlation between M1PAM binding affinity and functional activity, and that [3H]PT-1284 can serve as a tool for pharmacological investigation of M1mAChR PAMs.
Details
- Language :
- English
- ISSN :
- 0026895X and 15210111
- Volume :
- 90
- Issue :
- 3
- Database :
- Supplemental Index
- Journal :
- Molecular Pharmacology
- Publication Type :
- Periodical
- Accession number :
- ejs39851799
- Full Text :
- https://doi.org/10.1124/mol.116.104737