Mu-opioid receptors are widely distributed in the central and peripheral nervous system and upon activation have manifold actions including; depression of respiration, activation of the reward pathway, disruption of normal gastrointestinal motility and analgesia. Chronic administration of opioids results in a decline in the response (tolerance) the degree of which differs depending on the agonist and the measure under study. Analgesic tolerance to opioids limits the therapeutic efficacy. The link between the initial activation of receptors and the development of long-term tolerance is the subject of intense study and is dependent on multiple mechanisms. One repeatable and robust measure of opioid action measured on single cells is acute desensitization. This is thought to be an initial adaptive step in the pathway to cellular tolerance. Studies of desensitization have centered on (1) agonist occupancy (2) receptor phosphorylation (3) arrestin binding and (4) receptor internalization. By examining receptors where phosphorylation is blocked this proposal will determine the link between desensitization and the development of long-term tolerance. There are two possible outcomes. One is that the block of desensitization disrupts the development of long-term tolerance measured at the cellular level. The second is that the block of desensitization results in continued signaling that augments homeostatic mechanisms at the cellular and synaptic level that counter the continued activation of receptors. The results from this study will address a long-standing question surrounding the mechanisms that underlie a significant therapeutic problem with the use of opioids as analgesics.

Public Health Relevance

Opioids are used clinically for the treatment of acute and chronic pain. The development of tolerance is a limitation of these compounds. The results of this study will define the earliest agonist/receptor-dependent processes. Knowledge of these early events with acute application of agonists as well as the change in regulation following chronic treatment will facilitate the development of protocols for safe and effective treatment of pain.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA008163-27
Application #
9674404
Study Section
Molecular Neuropharmacology and Signaling Study Section (MNPS)
Program Officer
Sorensen, Roger
Project Start
1993-04-01
Project End
2022-03-31
Budget Start
2019-04-01
Budget End
2020-03-31
Support Year
27
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Oregon Health and Science University
Department
Neurosciences
Type
Overall Medical
DUNS #
096997515
City
Portland
State
OR
Country
United States
Zip Code
97239
Arttamangkul, Seksiri; Heinz, Daniel A; Bunzow, James R et al. (2018) Cellular tolerance at the µ-opioid receptor is phosphorylation dependent. Elife 7:
Levitt, Erica S; Williams, John T (2018) Desensitization and Tolerance of Mu Opioid Receptors on Pontine Kölliker-Fuse Neurons. Mol Pharmacol 93:8-13
Hunnicutt, Barbara J; Jongbloets, Bart C; Birdsong, William T et al. (2016) A comprehensive excitatory input map of the striatum reveals novel functional organization. Elife 5:
Arttamangkul, Seksiri; Birdsong, William; Williams, John T (2015) Does PKC activation increase the homologous desensitization of ? opioid receptors? Br J Pharmacol 172:583-92
Levitt, Erica S; Abdala, Ana P; Paton, Julian F R et al. (2015) ? opioid receptor activation hyperpolarizes respiratory-controlling Kölliker-Fuse neurons and suppresses post-inspiratory drive. J Physiol 593:4453-69
Birdsong, William T; Arttamangkul, Seksiri; Bunzow, James R et al. (2015) Agonist Binding and Desensitization of the ?-Opioid Receptor Is Modulated by Phosphorylation of the C-Terminal Tail Domain. Mol Pharmacol 88:816-24
Williams, John T (2014) Desensitization of functional µ-opioid receptors increases agonist off-rate. Mol Pharmacol 86:52-61
Birdsong, William T; Arttamangkul, Seksiri; Clark, Mary J et al. (2013) Increased agonist affinity at the ?-opioid receptor induced by prolonged agonist exposure. J Neurosci 33:4118-27
Banghart, Matthew R; Williams, John T; Shah, Ruchir C et al. (2013) Caged naloxone reveals opioid signaling deactivation kinetics. Mol Pharmacol 84:687-95
Arttamangkul, Seksiri; Lau, Elaine K; Lu, Hsin-Wei et al. (2012) Desensitization and trafficking of ýý-opioid receptors in locus ceruleus neurons: modulation by kinases. Mol Pharmacol 81:348-55

Showing the most recent 10 out of 52 publications