Opportunities and challenges for the development of M1 muscarinic receptor positive allosteric modulators in the treatment for neurocognitive deficits
- PMID: 36355830
- DOI: 10.1111/bph.15982
Opportunities and challenges for the development of M1 muscarinic receptor positive allosteric modulators in the treatment for neurocognitive deficits
Abstract
Targeting allosteric sites of M1 muscarinic acetylcholine receptors (M1 receptors) is a promising strategy to treat neurocognitive disorders, such as Alzheimer's disease and schizophrenia. Indeed, the last two decades have seen an impressive body of work focussing on the design and development of positive allosteric modulators (PAMs) for the M1 receptor. This has led to the identification of a structurally diverse range of highly selective M1 PAMs. In preclinical models, M1 PAMs have shown rescue of cognitive deficits and improvement of endpoints predictive of symptom domains of schizophrenia. Yet, to date only a few M1 PAMs have reached early-stage clinical trials, with many of them failing to progress further due to on-target mediated cholinergic adverse effects that have plagued the development of this class of ligand. This review covers the recent preclinical and clinical studies in the field of M1 receptor drug discovery for the treatment of Alzheimer's disease and schizophrenia, with a specific focus on M1 PAM, highlighting both the undoubted potential but also key challenges for the successful translation of M1 PAMs from bench-side to bedside. LINKED ARTICLES: This article is part of a themed issue Therapeutic Targeting of G Protein-Coupled Receptors: hot topics from the Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists 2021 Virtual Annual Scientific Meeting. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v181.14/issuetoc.
Keywords: M1 muscarinic acetylcholine receptors; allosteric modulators; cognitive deficits.
© 2022 British Pharmacological Society.
Similar articles
-
Diverse Effects on M1 Signaling and Adverse Effect Liability within a Series of M1 Ago-PAMs.ACS Chem Neurosci. 2017 Apr 19;8(4):866-883. doi: 10.1021/acschemneuro.6b00429. Epub 2017 Jan 10. ACS Chem Neurosci. 2017. PMID: 28001356 Free PMC article.
-
Development of M1 mAChR allosteric and bitopic ligands: prospective therapeutics for the treatment of cognitive deficits.ACS Chem Neurosci. 2013 Jul 17;4(7):1026-48. doi: 10.1021/cn400086m. Epub 2013 May 23. ACS Chem Neurosci. 2013. PMID: 23659787 Free PMC article. Review.
-
Probing the binding site of novel selective positive allosteric modulators at the M1 muscarinic acetylcholine receptor.Biochem Pharmacol. 2018 Aug;154:243-254. doi: 10.1016/j.bcp.2018.05.009. Epub 2018 May 17. Biochem Pharmacol. 2018. PMID: 29777683 Free PMC article.
-
M1 muscarinic acetylcholine receptors: A therapeutic strategy for symptomatic and disease-modifying effects in Alzheimer's disease?Adv Pharmacol. 2020;88:277-310. doi: 10.1016/bs.apha.2019.12.003. Epub 2020 Jan 27. Adv Pharmacol. 2020. PMID: 32416870 Review.
-
Therapeutic potential of TAK-071, a muscarinic M1 receptor positive allosteric modulator with low cooperativity, for the treatment of cognitive deficits and negative symptoms associated with schizophrenia.Neurosci Lett. 2021 Nov 1;764:136240. doi: 10.1016/j.neulet.2021.136240. Epub 2021 Sep 10. Neurosci Lett. 2021. PMID: 34509568
Cited by
-
Extrahelical Binding Site for a 1H-Imidazo[4,5-c]quinolin-4-amine A3 Adenosine Receptor Positive Allosteric Modulator on Helix 8 and Distal Portions of Transmembrane Domains 1 and 7.Mol Pharmacol. 2024 Feb 15;105(3):213-223. doi: 10.1124/molpharm.123.000784. Mol Pharmacol. 2024. PMID: 38182432 Free PMC article.
-
The potential of muscarinic M1 and M4 receptor activators for the treatment of cognitive impairment associated with schizophrenia.Front Psychiatry. 2024 Oct 4;15:1421554. doi: 10.3389/fpsyt.2024.1421554. eCollection 2024. Front Psychiatry. 2024. PMID: 39483736 Free PMC article. Review.
-
Muscarinic Receptors and Alzheimer's Disease: New Perspectives and Mechanisms.Curr Issues Mol Biol. 2024 Jul 2;46(7):6820-6835. doi: 10.3390/cimb46070407. Curr Issues Mol Biol. 2024. PMID: 39057049 Free PMC article. Review.
-
The Partial M1 Muscarinic Cholinergic Receptor Agonist, CDD-0102A, Differentially Modulates Glutamate Efflux in Striatal Subregions during Stereotyped Motor Behavior in the BTBR Mouse Model of Autism.ACS Chem Neurosci. 2023 Aug 2;14(15):2699-2709. doi: 10.1021/acschemneuro.3c00260. Epub 2023 Jul 11. ACS Chem Neurosci. 2023. PMID: 37434313 Free PMC article.
-
Role of Muscarinic Acetylcholine Receptors in Intestinal Epithelial Homeostasis: Insights for the Treatment of Inflammatory Bowel Disease.Int J Mol Sci. 2023 Mar 30;24(7):6508. doi: 10.3390/ijms24076508. Int J Mol Sci. 2023. PMID: 37047478 Free PMC article. Review.
References
REFERENCES
-
- Abd‐Elrahman, K. S., Sarasija, S., Colson, T. L., & Ferguson, S. S. G. (2022). A positive allosteric modulator for the muscarinic receptor (M1 mAChR) improves pathology and cognitive deficits in female APPswe/PSEN1ΔE9 mice. British Journal of Pharmacology, 179(8), 1769–1783. https://doi.org/10.1111/bph.15750
-
- Abdel‐wahab, B. A., & Abdel‐wahab, M. M. (2016). Protective effect of resveratrol against chronic intermittent hypoxia‐induced spatial memory deficits, hippocampal oxidative DNA damage and increased p47Phox NADPH oxidase expression in young rats. Behavioural Brain Research, 305, 65–75. https://doi.org/10.1016/j.bbr.2016.02.030
-
- Abdul‐Ridha, A., Lane, J. R., Mistry, S. N., López, L., Sexton, P. M., Scammells, P. J., Christopoulos, A., & Canals, M. (2014). Mechanistic insights into allosteric structure‐function relationships at the M1 muscarinic acetylcholine receptor. Journal of Biological Chemistry, 289(48), 33701–33711. https://doi.org/10.1074/jbc.M114.604967
-
- Abdul‐Ridha, A., Lane, J. R., Sexton, P. M., Canals, M., & Christopoulos, A. (2013). Allosteric modulation of a chemogenetically modified G protein‐coupled receptor. Molecular Pharmacology, 83(2), 521–530. https://doi.org/10.1124/mol.112.083006
-
- Abrams, P., Andersson, K., Buccafusco, J. J., Chapple, C., Chet, W., Groat, D., Fryer, A. D., Kay, G., Laties, A., Nathanson, N. M., Pasricha, P. J., & Wein, A. J. (2006). Muscarinic receptors: Their distribution and function in body systems, and the implications for treating overactive bladder. British Journal of Pharmacology, 148, 565–578. https://doi.org/10.1038/sj.bjp.0706780
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous