Src-dependent phosphorylation of μ-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 μ-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 i

SUBMITTER: Zhang L 

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

REPOSITORIES: biostudies-literature