Parameter-specific analgesic effects of electroacupuncture mediated by degree of regulation TRPV1 and P2X3 in inflammatory pain in rats

Life Sci. 2018 May 1:200:69-80. doi: 10.1016/j.lfs.2018.03.028. Epub 2018 Mar 14.

Abstract

Aims: Observing the parameter-specific anti-hyperalgesic effects of EA with different stimulation times and frequencies on painful hyperalgesia mediated by the level of TRPV1 and P2X3 expression in DRG after CFA injection.

Main methods: The model was induced by the injection of CFA in each rat's right hind paw. EA treatment was applied to the bilateral ST36 and BL60. Paw withdrawal threshold (PWT) and paw withdrawal latency (PWL) were tested with Von Frey filaments and the radiant heat source of the test instrument, respectively. TRPV1 and P2X3 expressions were measured by immunofluorescence and western blot. αβ-meATP and capsaicine combined with EA were further utilized to investigate the change in PWL.

Key findings: Different stimulation times (20, 30, 45 min) combined with different frequencies (2 Hz, 100 Hz, 2/100 Hz) of EA have analgesic effects on the PWT and PWL; however, the level of the hypoalgesic efficacy of EA was primarily associated with EA frequency. The analgesic effect of EA was better at 100 Hz than at 2 Hz. The level of regulation of 100 Hz EA on TRPV1 and P2X3 in DRG was greater than that of 2 Hz. Furthermore, both TRPV1 agonist and P2X3 agonist may impair the level of EA analgesia.

Significance: EA has a parameter-specific effect on chronic inflammatory pain relief, which primarily depend on the stimulation frequency and not on the stimulation time at a certain stimulation time. The parameter-specific analgesic effect of EA is at least partially related to mediation of the protein level of TRPV1 and P2X3 expression in DRG of CFA rats.

Keywords: Electroacupuncture; Frequency-specific; Inflammatory pain; P2X3; TRPV1.

MeSH terms

  • Animals
  • Disease Models, Animal
  • Electroacupuncture*
  • Ganglia, Spinal / metabolism*
  • Ganglia, Spinal / pathology
  • Ganglia, Spinal / physiopathology
  • Gene Expression Regulation*
  • Hyperalgesia / chemically induced
  • Hyperalgesia / metabolism*
  • Hyperalgesia / physiopathology
  • Hyperalgesia / therapy*
  • Male
  • Pain / chemically induced
  • Pain / metabolism*
  • Pain / pathology
  • Pain / physiopathology
  • Pain Management*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Purinergic P2X3 / biosynthesis*
  • TRPV Cation Channels / biosynthesis*

Substances

  • Receptors, Purinergic P2X3
  • TRPV Cation Channels
  • Trpv1 protein, rat