Home > Mechanism of opioid addiction and its intervention therapy: focusing on the reward circuitry and mu-opioid receptor.

Zhang, Jia-Jia and Song, Chang-Geng and Dai, Ji-Min and Li, Ling and Yang, Xiang-Min and Chen, Zhi-Nan (2022) Mechanism of opioid addiction and its intervention therapy: focusing on the reward circuitry and mu-opioid receptor. MedComm, 3, (3), e148. doi: 10.1002/mco2.148.

External website: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC92185...

Opioid abuse and addiction have become a global pandemic, posing tremendous health and social burdens. The rewarding effects and the occurrence of withdrawal symptoms are the two mainstays of opioid addiction. Mu-opioid receptors (MORs), a member of opioid receptors, play important roles in opioid addiction, mediating both the rewarding effects of opioids and opioid withdrawal syndrome (OWS). The underlying mechanism of MOR-mediated opioid rewarding effects and withdrawal syndrome is of vital importance to understand the nature of opioid addiction and also provides theoretical basis for targeting MORs to treat drug addiction.

In this review, we first briefly introduce the basic concepts of MORs, including their structure, distribution in the nervous system, endogenous ligands, and functional characteristics. We focused on the brain circuitry and molecular mechanism of MORs-mediated opioid reward and withdrawal. The neuroanatomical and functional elements of the neural circuitry of the reward system underlying opioid addiction were thoroughly discussed, and the roles of MOR within the reward circuitry were also elaborated. Furthermore, we interrogated the roles of MORs in OWS, along with the structural basis and molecular adaptions of MORs-mediated withdrawal syndrome. Finally, current treatment strategies for opioid addiction targeting MORs were also presented.


Item Type
Article
Publication Type
International, Open Access, Review, Article
Drug Type
Opioid
Intervention Type
Screening / Assessment
Date
September 2022
Identification #
doi: 10.1002/mco2.148
Volume
3
Number
3
EndNote

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