Electroacupuncture suppresses the pain and pain-related anxiety of chronic inflammation in rats by increasing the expression of the NPS/NPSR system in the ACC

Brain Res. 2020 Apr 15:1733:146719. doi: 10.1016/j.brainres.2020.146719. Epub 2020 Feb 7.

Abstract

Background: The neuropeptide S/Neuropeptide S receptor (NPS/NPSR) system is involved in the regulation of anxiety in rodents. Chronic inflammation can induce anxiety. Our lab has observed that electroacupuncture (EA) has a beneficial effect on chronic inflammatory pain and pain-related anxiety; however, the mechanism should be further clarified. In the present study, we used an inflammatory pain model to investigate the role of the NPS/NPSR system in the anterior cingulate cortex (ACC) in the analgesic and antianxiety effects of EA.

Results: In an inflammatory pain model, the paw withdrawal thresholds (PWTs) were decreased, pain-related anxiety-like behaviors were induced, and the ipsilateral protein expression of NPS and NPSR was decreased in the ACC. EA stimulation increased the PWTs, reduced pain-related anxiety-like behavior, and enhanced the ipsilateral protein expression of NPS and NPSR in the ACC. NPS microinjection increased the PWTs and decreased pain-related anxiety-like behaviors. Furthermore, an NPSR inhibitor combined with EA reversed the effect of EA on the PWTs and pain-related anxiety-like behaviors.

Conclusions: Our results suggest that EA suppresses pain and pain-related anxiety-like behavior of chronic inflammation in rats by increasing the expression of the NPS/NPSR system in the ACC.

Keywords: ACC; Electroacupuncture; NPS/NPSR system; Pain; Pain-related anxiety-like behavior.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anxiety / complications
  • Anxiety / metabolism*
  • Electroacupuncture*
  • Gyrus Cinguli / metabolism*
  • Inflammation / complications
  • Inflammation / metabolism*
  • Male
  • Neuropeptides / metabolism*
  • Pain / complications
  • Pain / metabolism*
  • Pain Threshold
  • Rats, Sprague-Dawley
  • Receptors, Neuropeptide / metabolism*

Substances

  • Neuropeptides
  • Receptors, Neuropeptide
  • neuropeptide S receptor, rat
  • neuropeptide S, rat