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Updated: Jul 25, 2025

Assessment of Morphine-induced Hyperalgesia and Analgesic Tolerance in Mice Using Thermal and Mechanical Nociceptive Modalities
Published on: July 29, 2014
Brainstem Modulation of Nociception by Periaqueductal Gray Neurons Expressing the μ-Opioid Receptor in Mice
Eileen Nguyen1, Michael C Chiang2, Catherine Nguyen2
1Department of Anesthesiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania; Department of Neurobiology, University of Pittsburgh, Pittsburgh, Pennsylvania; Department of Anesthesiology, University of California-Los Angeles, Los Angeles, California.
Background:
Pharmacologic manipulations directed at the periaqueductal gray have demonstrated the importance of the μ-opioid receptor in modulating reflexive responses to nociception. The authors hypothesized that a supraspinal pathway centered on neurons in the periaqueductal gray containing the μ-opioid receptor could modulate nociceptive and itch behaviors.
Methods:
The study used anatomical, optogenetic, and chemogenetic approaches in male and female mice to manipulate μ-opioid receptor neurons in the periaqueductal gray. Behavioral assays including von Frey, Hargreaves, cold plantar, chloroquine-induced itch, hotplate, formalin-induced injury, capsaicin-induced injury, and open field tests were used. In separate experiments, naloxone was administered in a postsurgical model of latent sensitization.
Results:
Activation of μ-opioid receptor neurons in the periaqueductal gray increased jumping (least-squares mean difference of -3.30 s; 95% CI, -6.17 to -0.44; P = 0.023; n = 7 or 8 mice per group), reduced itch responses (least-squares mean difference of 70 scratching bouts; 95% CI, 35 to 105; P < 0.001; n = 8 mice), and elicited modestly antinociceptive effects (least-squares mean difference of -0.7 g on mechanical and -10.24 s on thermal testing; 95% CI, -1.3 to -0.2 and 95% CI, -13.77 to -6.70, and P = 0.005 and P < 0.001, respectively; n = 8 mice). Last, the study uncovered the role of the periaqueductal gray in suppressing hyperalgesia after a postsurgical state of latent sensitization (least-squares mean difference comparing saline and naloxone of -12 jumps; 95% CI, -17 to -7; P < 0.001 for controls; and -2 jumps; 95% CI, -7 to 4; P = 0.706 after optogenetic stimulation; n = 7 to 9 mice per group).
Conclusions:
μ-Opioid receptor neurons in the periaqueductal gray modulate distinct nocifensive behaviors: their activation reduced responses to mechanical and thermal testing, and attenuated scratching behaviors, but facilitated escape responses. The findings emphasize the role of the periaqueductal gray in the behavioral expression of nociception using reflexive and noxious paradigms.
Insights
Activation of μ-opioid receptor neurons in the periaqueductal gray modulates pain and itch behaviors. This study highlights the periaqueductal gray's role in expressing nociception through reflexive and noxious responses.
Area of Science:
- Neuroscience
- Pain Research
- Behavioral Science
Background:
- Periaqueductal gray (PAG) involvement in pain modulation is established.
- μ-opioid receptors (MOR) within the PAG are crucial for processing nociception.
- A supraspinal pathway involving PAG MOR neurons may regulate nociceptive and itch behaviors.
Purpose of the Study:
- To investigate the role of μ-opioid receptor neurons in the periaqueductal gray (PAG) in modulating nociceptive and itch behaviors.
- To elucidate the specific behavioral outputs influenced by PAG MOR activation.
- To examine the PAG's function in suppressing post-surgical hyperalgesia.
Main Methods:
- Utilized anatomical, optogenetic, and chemogenetic techniques in mice.
- Employed a battery of behavioral assays including mechanical/thermal nociception tests, itch assays, and open field tests.
- Administered naloxone in a postsurgical latent sensitization model.
Main Results:
- PAG MOR neuron activation reduced responses to mechanical and thermal stimuli.
- Activation attenuated scratching behaviors associated with itch.
- PAG MOR neuron activation facilitated escape responses and suppressed post-surgical hyperalgesia.
Conclusions:
- PAG MOR neurons play a significant role in modulating diverse nocifensive behaviors.
- Activation of PAG MOR neurons can reduce pain and itch but increase escape behaviors.
- The PAG is critical for the behavioral expression of nociception in various paradigms.
Related Concept Videos
Analgesia and Pain Management
Opioid Receptors: Overview
Nociception
Pain

