Identification of Positive Allosteric Modulators of the D 1 Dopamine Receptor That Act at Diverse Binding Sites

• Published in: Molecular pharmacology 2018-10, Vol.94 (4), p.1197-1209
• Main Authors: Luderman, Kathryn D, Conroy, Jennie L, Free, R Benjamin, Southall, Noel, Ferrer, Marc, Sanchez-Soto, Marta, Moritz, Amy E, Willette, Blair K A, Fyfe, Tim J, Jain, Prashi, Titus, Steve, Hazelwood, Lisa A, Aubé, Jeffrey, Lane, J Robert, Frankowski, Kevin J, Sibley, David R
• Format: Article
• Language: English
• Subjects: Allosteric Regulation - physiology; Allosteric Site - physiology; Animals; beta-Arrestins - metabolism; CHO Cells; Cricetulus; Cyclic AMP - metabolism; Dopamine - metabolism; GTP-Binding Proteins - metabolism; HEK293 Cells; Humans; Receptors, Dopamine - metabolism; Signal Transduction - physiology
• ISSN: 0026-895X; 1521-0111
• DOI: 10.1124/mol.118.113175

The D dopamine receptor is linked to a variety of neuropsychiatric disorders and represents an attractive drug target for the enhancement of cognition in schizophrenia, Alzheimer disease, and other disorders. Positive allosteric modulators (PAMs), with their potential for greater selectivity and larger therapeutic windows, may represent a viable drug development strategy, as orthosteric D receptor agonists possess known clinical liabilities. We discovered two structurally distinct D receptor PAMs, MLS6585 and MLS1082, via a high-throughput screen of the NIH Molecular Libraries program small-molecule library. Both compounds potentiate dopamine-stimulated G protein- and -arrestin-mediated signaling and increase the affinity of dopamine for the D receptor with low micromolar potencies. Neither compound displayed any intrinsic agonist activity. Both compounds were also found to potentiate the efficacy of partial agonists. We tested maximally effective concentrations of each PAM in combination to determine if the compounds might act at separate or similar sites. In combination, MLS1082 + MLS6585 produced an additive potentiation of dopamine potency beyond that caused by either PAM alone for both -arrestin recruitment and cAMP accumulation, suggesting diverse sites of action. In addition, MLS6585, but not MLS1082, had additive activity with the previously described D receptor PAM "Compound B," suggesting that MLS1082 and Compound B may share a common binding site. A point mutation (R130Q) in the D receptor was found to abrogate MLS1082 activity without affecting that of MLS6585, suggesting this residue may be involved in the binding/activity of MLS1082 but not that of MLS6585. Together, MLS1082 and MLS6585 may serve as important tool compounds for the characterization of diverse allosteric sites on the D receptor as well as the development of optimized lead compounds for therapeutic use.