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Src-dependent phosphorylation of ?-opioid receptor at Tyr336 modulates opiate withdrawal.


ABSTRACT: Opiate withdrawal/negative reinforcement has been implicated as one of the mechanisms for the progression from impulsive to compulsive drug use. Increase in the intracellular cAMP level and protein kinase A (PKA) activities within the neurocircuitry of addiction has been a leading hypothesis for opiate addiction. This increase requires the phosphorylation of ?-opioid receptor (MOR) at Tyr336 by Src after prolonged opiate treatment in vitro Here, we report that the Src-mediated MOR phosphorylation at Tyr336 is a prerequisite for opiate withdrawal in mice. We observed the recruitment of Src in the vicinity of MOR and an increase in phosphorylated Tyr336 (pY336) levels during naloxone-precipitated withdrawal. The intracerebroventricular or stereotaxic injection of a Src inhibitor (AZD0530), or Src shRNA viruses attenuated pY336 levels, and several somatic withdrawal signs. This was also observed in Fyn-/- mice. The stereotaxic injection of wild-type MOR, but not mutant (Y336F) MOR, lentiviruses into the locus coeruleus of MOR-/- mice restored somatic withdrawal jumping. Regulating pY336 levels during withdrawal might be a future target for drug development to prevent opiate addictive behaviors.

SUBMITTER: Zhang L 

PROVIDER: S-EPMC5666313 | biostudies-literature | 2017 Nov

REPOSITORIES: biostudies-literature

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Src-dependent phosphorylation of μ-opioid receptor at Tyr<sup>336</sup> modulates opiate withdrawal.

Zhang Lei L   Kibaly Cherkaouia C   Wang Yu-Jun YJ   Xu Chi C   Song Kyu Young KY   McGarrah Patrick W PW   Loh Horace H HH   Liu Jing-Gen JG   Law Ping-Yee PY  

EMBO molecular medicine 20171101 11


Opiate withdrawal/negative reinforcement has been implicated as one of the mechanisms for the progression from impulsive to compulsive drug use. Increase in the intracellular cAMP level and protein kinase A (PKA) activities within the neurocircuitry of addiction has been a leading hypothesis for opiate addiction. This increase requires the phosphorylation of μ-opioid receptor (MOR) at Tyr<sup>336</sup> by Src after prolonged opiate treatment <i>in vitro</i> Here, we report that the Src-mediated  ...[more]

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