4.2 Article

Electroacupuncture Inhibits the Interaction between Peripheral TRPV1 and P2X3 in Rats with Different Pathological Pain

Journal

PHYSIOLOGICAL RESEARCH
Volume 70, Issue 4, Pages 635-647

Publisher

ACAD SCIENCES CZECH REPUBLIC, INST PHYSIOLOGY
DOI: 10.33549/physiolres.934649

Keywords

Electroacupuncture; Interaction; TRPV1; Chronic inflammatory pain; Chronic neuropathic pain

Categories

Funding

  1. National Natural Science Fund of China [81473772, 81603690, 81603676]
  2. Major Medical and Health Science and Technology Project of Zhejiang Province [WKJ-ZJ-1419]
  3. Zhejiang Provincial Natural Science Fund of China [LQ15H270003]
  4. Key Science and Technology Innovation Team of Zhejiang Province [2013TD15]
  5. Zhejiang Provincial Natural Science Funds for Distinguished Young Scholars [LR17H270001]

Ask authors/readers for more resources

The study demonstrated that 100Hz and 2Hz electroacupuncture stimulation can effectively reduce hyperalgesia in rats with inflammatory and neuropathic pain. This effect is partly achieved by inhibiting the co-expression and indirect interaction between peripheral TRPV1 and P2X3.
Chronic pain is regarded to be one of the common and refractory diseases to cure in the clinic. One hundred Hz electroacupuncture (EA) is commonly used for inflammatory pain and 2 Hz for neuropathic pain possibly by modulating the transient receptor potential vanilloid subtype 1 (TRPV1) or the purinergic P2X3 related pathways. To clarify the mechanism of EA under various conditions of pathological pain, rats received a subcutaneous administration of complete Freund's adjuvant (CFA) for inflammatory pain and spared nerve injury (SNI) for neuropathic pain. The EA was performed at the bilateral ST36 and BL60 1 d after CFA or SNI being successfully established for 3 consecutive days. The mechanical hyperalgesia test was measured at baseline, 1 d after model establishment, 1 d and 3 d after EA. The co-expression changes, co-immunoprecipitation of TRPV1 and P2X3, and spontaneous pain behaviors (SPB) test were performed 3 d after EA stimulation. One hundred Hz EA or 2Hz EA stimulation could effectively down-regulate the hyperalgesia of CFA or SNI rats. The increased co-expression ratio between TRPV1 and P2X3 at the dorsal root ganglion (DRG) in two types of pain could be reduced by 100Hz or 2Hz EA intervention. While 100Hz or 2Hz EA was not able to eliminate the direct physical interaction between TRPV1 and P2X3. Moreover, EA could significantly inhibit the SPB induced by the co-activation of peripheral TRPV1 and P2X3. All results indicated that EA could significantly reduce the hyperalgesia and the SPB, which was partly related to inhibiting the co-expression and indirect interaction between peripheral TRPV1 and P2X3.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available