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Updated: Aug 15, 2026

Assessment of Morphine-induced Hyperalgesia and Analgesic Tolerance in Mice Using Thermal and Mechanical Nociceptive Modalities
Published on: July 29, 2014
Inescapable shock-induced potentiation of morphine analgesia in rats: sites of action
S E Hammack1, C E Hartley, S E Lea
1Department of Psychology, University of Colorado, 80309-0345, USA. jom@clipr.colorado.edu
Abstract:
Inescapable shock (IS) enhances analgesia to systemic morphine (MOR) 24 hr later. IS activates serotonin neurons in the dorsal raphe nucleus (DRN), rendering them hyperexcitable. These studies tested whether IS potentiates the analgesic effect of MOR microinjected in the DRN, as predicted by this hypothesis. To test site specificity, the effect of previous IS was examined on MOR microinjected lateral to the DRN and into 2 other sites that support MOR analgesia, the nucleus raphe magnus (NRM) and spinal cord. Twenty-four hours after IS, potentiated analgesia was observed after 0.5 microg MOR microinjected into, but not lateral to, the DRN. Potentiated analgesia was also observed after NRM (1.0 microg) and spinal cord (3.0 microg) MOR microinjections. These data suggest that IS-induced excitability changes within the DRN synergize with opiates microinjected in other analgesia areas and that this potentiates the responses to opiates 24 hr after IS.
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