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

被引:7
|
作者
Wei, Siqi [1 ,2 ,4 ]
Chang, Shuyang [1 ,2 ]
Dong, Yue [1 ,2 ]
Xu, Linping [1 ,2 ]
Yuan, Xiaocui [1 ,2 ]
Jia, Hong [1 ,2 ]
Zhang, Jun [3 ]
Liang, Lingli [1 ,2 ,5 ]
机构
[1] Xi An Jiao Tong Univ, Inst Neurosci, Translat Med Inst, Hlth Sci Ctr, Xian, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Basic Med Sci, Dept Physiol & Pathophysiol, Hlth Sci Ctr, Xian, Shaanxi, Peoples R China
[3] Nankai Univ, Tianjin Union Med Ctr, Dept Pain Med, Tianjin, Peoples R China
[4] Xi An Jiao Tong Univ, Res Ctr Stomatol, Key Lab Shaanxi Prov Craniofacial Precis Med Res, Coll Stomatol, Xian, Shaanxi, Peoples R China
[5] Xi An Jiao Tong Univ, Minist Educ, Key Lab Environm & Genes Related Dis, Beijing, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
AXL; Electro-acupuncture; Neuropathic pain; Spinal nerve ligation; RECEPTOR TYROSINE KINASES; GROWTH-FACTOR; NEUROTROPHIC FACTOR; TAM RECEPTORS; GAS6; NGF; ACTIVATION; IDENTIFICATION; INFLAMMATION; PREVALENCE;
D O I
10.1007/s11064-020-03185-x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:504 / 512
页数:9
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