| Literature DB >> 27119457 |
Larry S Barak1, Yushi Bai1, Sean Peterson1, Tama Evron1, Nikhil M Urs1, Satyamaheshwar Peddibhotla2, Michael P Hedrick3, Paul Hershberger2, Patrick R Maloney2, Thomas D Y Chung3, Ramona M Rodriguiz1, William C Wetsel1, James B Thomas4, Glen R Hanson5, Anthony B Pinkerton3, Marc G Caron1.
Abstract
Pharmacological treatment for methamphetamine addiction will provide important societal benefits. Neurotensin receptor NTR1 and dopamine receptor distributions coincide in brain areas regulating methamphetamine-associated reward, and neurotensin peptides produce behaviors opposing psychostimulants. Therefore, undesirable methamphetamine-associated activities should be treatable with druggable NTR1 agonists, but no such FDA-approved therapeutics exist. We address this limitation with proof-of-concept data for ML314, a small-molecule, brain penetrant, β-arrestin biased, NTR1 agonist. ML314 attenuates amphetamine-like hyperlocomotion in dopamine transporter knockout mice, and in C57BL/6J mice it attenuates methamphetamine-induced hyperlocomotion, potentiates the psychostimulant inhibitory effects of a ghrelin antagonist, and reduces methamphetamine-associated conditioned place preference. In rats, ML314 blocks methamphetamine self-administration. ML314 acts as an allosteric enhancer of endogenous neurotensin, unmasking stoichiometric numbers of hidden NTR1 binding sites in transfected-cell membranes or mouse striatal membranes, while additionally supporting NTR1 endocytosis in cells in the absence of NT peptide. These results indicate ML314 is a viable, preclinical lead for methamphetamine abuse treatment and support an allosteric model of G protein-coupled receptor signaling.Entities:
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Year: 2016 PMID: 27119457 PMCID: PMC4947017 DOI: 10.1021/acschembio.6b00291
Source DB: PubMed Journal: ACS Chem Biol ISSN: 1554-8929 Impact factor: 5.100