دورية أكاديمية

Identification and pharmacological profile of SPP1, a potent, functionally selective and brain penetrant agonist at muscarinic M1 receptors.

التفاصيل البيبلوغرافية
العنوان: Identification and pharmacological profile of SPP1, a potent, functionally selective and brain penetrant agonist at muscarinic M1 receptors.
المؤلفون: Broad, Lisa M1 broad_lisa@lilly.com, Sanger, Helen E1, Mogg, Adrian J1, Colvin, Ellen M1, Zwart, Ruud1, Evans, David A1, Pasqui, Francesca1, Sher, Emanuele1, Wishart, Graham N1, Barth, Vanessa N2, Felder, Christian C2, Goldsmith, Paul J1
المصدر: British Journal of Pharmacology. Jan2019, Vol. 176 Issue 1, p110-126. 17p. 2 Diagrams, 3 Charts, 8 Graphs.
مصطلحات موضوعية: *ALZHEIMER'S disease treatment, *MUSCARINIC receptors, *MUSCARINIC agonists, *PHARMACOLOGY, *LABORATORY rats
مستخلص: Background and Purpose: We aimed to identify and develop novel, selective muscarinic M1 receptor agonists as potential therapeutic agents for the symptomatic treatment of Alzheimer's disease. Experimental Approach We developed and utilized a novel M1 receptor occupancy assay to drive a structure activity relationship in a relevant brain region while simultaneously tracking drug levels in plasma and brain to optimize for central penetration. Functional activity was tracked in relevant native in vitro assays allowing translational (rat–human) benchmarking of structure–activity relationship molecules to clinical comparators. Key Results: Using this paradigm, we identified a series of M1 receptor selective molecules displaying desirable in vitro and in vivo properties and optimized key features, such as central penetration while maintaining selectivity and a partial agonist profile. From these compounds, we selected spiropiperidine 1 (SPP1). In vitro, SPP1 is a potent, partial agonist of cortical and hippocampal M1 receptors with activity conserved across species. SPP1 displays high functional selectivity for M1 receptors over native M2 and M3 receptor anti‐targets and over a panel of other targets. Assessment of central target engagement by receptor occupancy reveals SPP1 significantly and dose‐dependently occupies rodent cortical M1 receptors. Conclusions and Implications: We report the discovery of SPP1, a novel, functionally selective, brain penetrant partial orthosteric agonist at M1 receptors, identified by a novel receptor occupancy assay. SPP1 is amenable to in vitro and in vivo study and provides a valuable research tool to further probe the role of M1 receptors in physiology and disease. [ABSTRACT FROM AUTHOR]
قاعدة البيانات: Academic Search Index
الوصف
تدمد:00071188
DOI:10.1111/bph.14510