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Different neuronal populations mediate inflammatory pain analgesia by exogenous and endogenous opioids.


ABSTRACT: Mu-opioid receptors (MORs) are crucial for analgesia by both exogenous and endogenous opioids. However, the distinct mechanisms underlying these two types of opioid analgesia remain largely unknown. Here, we demonstrate that analgesic effects of exogenous and endogenous opioids on inflammatory pain are mediated by MORs expressed in distinct subpopulations of neurons in mice. We found that the exogenous opioid-induced analgesia of inflammatory pain is mediated by MORs in Vglut2+ glutamatergic but not GABAergic neurons. In contrast, analgesia by endogenous opioids is mediated by MORs in GABAergic rather than Vglut2+ glutamatergic neurons. Furthermore, MORs expressed at the spinal level is mainly involved in the analgesic effect of morphine in acute pain, but not in endogenous opioid analgesia during chronic inflammatory pain. Thus, our study revealed distinct mechanisms underlying analgesia by exogenous and endogenous opioids, and laid the foundation for further dissecting the circuit mechanism underlying opioid analgesia.

SUBMITTER: Zhang XY 

PROVIDER: S-EPMC7311172 | biostudies-literature | 2020 Jun

REPOSITORIES: biostudies-literature

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Different neuronal populations mediate inflammatory pain analgesia by exogenous and endogenous opioids.

Zhang Xin-Yan XY   Dou Yan-Nong YN   Yuan Lei L   Li Qing Q   Zhu Yan-Jing YJ   Wang Meng M   Sun Yan-Gang YG  

eLife 20200610


Mu-opioid receptors (MORs) are crucial for analgesia by both exogenous and endogenous opioids. However, the distinct mechanisms underlying these two types of opioid analgesia remain largely unknown. Here, we demonstrate that analgesic effects of exogenous and endogenous opioids on inflammatory pain are mediated by MORs expressed in distinct subpopulations of neurons in mice. We found that the exogenous opioid-induced analgesia of inflammatory pain is mediated by MORs in Vglut2<sup>+</sup> glutam  ...[more]

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