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Acute morphine induces matrix metalloproteinase-9 up-regulation in primary sensory neurons to mask opioid-induced analgesia in mice.

Yen-Chin Liu | Temugin Berta | Tong Liu | Ping-Heng Tan | Ru-Rong Ji
Molecular pain | 2012

Despite decades of intense research efforts, actions of acute opioids are not fully understood. Increasing evidence suggests that in addition to well-documented antinociceptive effects opioids also produce paradoxical hyperalgesic and excitatory effects on neurons. However, most studies focus on the pronociceptive actions of chronic opioid exposure. Matrix metalloproteinase 9 (MMP-9) plays an important role in neuroinflammation and neuropathic pain development. We examined MMP-9 expression and localization in dorsal root ganglia (DRGs) after acute morphine treatment and, furthermore, the role of MMP-9 in modulating acute morphine-induced analgesia and hyperalgesia in mice.

Pubmed ID: 22444868

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Associated grants

  • Agency: NINDS NIH HHS, United States
    Id: R01 NS067686
  • Agency: NINDS NIH HHS, United States
    Id: NS67686
  • Agency: NIDCR NIH HHS, United States
    Id: DE17794
  • Agency: NINDS NIH HHS, United States
    Id: NS54932

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