Brainstem Modulation of Nociception by Periaqueductal Gray Neurons Expressing the μ-Opioid Receptor in Mice

Author:

Nguyen Eileen1,Chiang Michael C.2,Nguyen Catherine3,Ross Sarah E.4

Affiliation:

1. 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.

2. 2Department of Anesthesiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania; Department of Neurobiology, University of Pittsburgh, Pittsburgh, Pennsylvania.

3. 3Department of Anesthesiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania; Department of Neurobiology, University of Pittsburgh, Pittsburgh, Pennsylvania.

4. 4Department of Anesthesiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania; Department of Neurobiology, University of Pittsburgh, Pittsburgh, Pennsylvania.

Abstract

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. Editor’s Perspective What We Already Know about This Topic What This Article Tells Us That Is New

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Anesthesiology and Pain Medicine

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