4.5 Article

Electro-acupuncture Suppresses AXL Expression in Dorsal Root Ganglion Neurons and Enhances Analgesic Effect of AXL Inhibitor in Spinal Nerve Ligation Induced-Neuropathic Pain Rats

Journal

NEUROCHEMICAL RESEARCH
Volume 46, Issue 3, Pages 504-512

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11064-020-03185-x

Keywords

AXL; Electro-acupuncture; Neuropathic pain; Spinal nerve ligation

Funding

  1. Key Projects of National Health and Family Planning Commission of Tianjin, China [16KG157]
  2. National Natural Science Foundation of China [81701112, 31871065]
  3. Natural Science Foundation of Shaanxi Province [2019JM-128]
  4. China Postdoctoral Science Foundation [2018M633527]
  5. Shaanxi Province Postdoctoral Science Foundation [2018BSHEDZZ147]

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The study indicates that electro-acupuncture can alleviate neuropathic pain by inhibiting the AXL signaling pathway, and the combination of AXL inhibitor and electro-acupuncture may have a synergistic effect, providing a new strategy for clinical treatment of neuropathic pain.
Electro-acupuncture (EA) has been used for clinic analgesia for many years. However, its mechanisms are not fully understood. We recently reported that AXL, a tyrosine kinase receptor, contributes to the peripheral mechanism of neuropathic pain. We here aim to figure out the significance of EA on neuropathic pain mediated by AXL in dorsal root ganglion (DRG). Spinal nerve ligation (SNL) was used as a neuropathic pain model. EA was applied at ''Huantiao'' (GB-30) and ''Yanglingquan'' (GB-34) acupoints for 30 min daily from day 7 to day 10 after SNL. EA not only gradually attenuated SNL-induced mechanical allodynia, but also suppressed the expression of phosphorylated AXL (p-AXL) and AXL in injured DRGs of SNL rats examined by western blotting and immunofluorescence. Moreover, intrathecal injection of the subthreshold dose of AXL inhibitor TP0903, significantly prolonged the analgesic time of single EA treatment and enhanced the analgesic effect of repeated EA treatments, suggesting a synergic effect of EA and AXL inhibitor. These results indicate that AXL signaling underlies EA analgesia and combination of AXL inhibitor and EA might be a new strategy for clinic analgesia on neuropathic pain.

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