Spinal Neuronal miR-124 Inhibits Microglial Activation and Contributes to Preventive Effect of Electroacupuncture on Chemotherapy-Induced Peripheral Neuropathy in Mice

被引:7
作者
Li, Xiao-Chen [1 ]
Chen, Hui [1 ]
Chen, Yu [1 ]
Chu, Yu-Xia [1 ,2 ]
Mi, Wen -Li [1 ,2 ]
Wang, Yan-Qing [1 ,2 ,3 ,4 ]
Mao-Ying, Qi-Liang [1 ,2 ,5 ]
机构
[1] Fudan Univ, Inst Acupuncture Res, Inst Integrat Med, Shanghai Med Coll,Dept Integrat Med & Neurobiol,Sc, Shanghai, Peoples R China
[2] Fudan Univ, Shanghai Key Lab Acupuncture Mech & Acupoint Funct, Shanghai, Peoples R China
[3] Fudan Univ, Inst Brain Sci, State Key Lab Med Neurobiol, Shanghai, Peoples R China
[4] Fudan Univ, Inst Brain Sci, MOE Frontiers Ctr Brain Sci, Shanghai, Peoples R China
[5] Fudan Univ, Sch Basic Med Sci, Dept Integrat Med & Neurobiol, POB 291,138 Yi Xue Yuan Rd, Shanghai 200032, Peoples R China
关键词
MICRORNAS; ACUPUNCTURE; MACROPHAGES; EXPRESSION; SYSTEM;
D O I
10.4049/jimmunol.2300539
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chemotherapy -induced peripheral neuropathy (CIPN) is a persistent and irreversible side effect of antineoplastic agents. Patients with CIPN usually show chronic pain and sensory deficits with glove -and -stocking distribution. However, whether spinal neuronal microRNA (miR)-124 is involved in cisplatin-induced peripheral neuropathy remains to be studied. In this study, miR-124 was significantly reduced in the spinal dorsal horn in CIPN mice. Overexpression of neuronal miR-124 induced by injecting adenoassociated virus with neuron -specific promoter into the spinal cord of mice prevented the development of mechanical allodynia, sensory deficits, and the loss of intraepidermal nerve fibers induced by cisplatin. Meanwhile, cisplatin-induced M1 microglia activation and the release of proinflammatory cytokines were significantly inhibited by overexpression of neuronal miR-124. Furthermore, electroacupuncture (EA) treatment upregulated miR-124 expression in the spinal dorsal horn of CIPN mice. Interestingly, downregulation of spinal neuronal miR-124 significantly inhibited the regulatory effect of EA on CIPN and microglia activity as well as spinal neuroinflammation induced by cisplatin. These results demonstrate that spinal neuronal miR-124 is involved in the prevention and treatment of EA on cisplatin-induced peripheral neuropathy in mice. Our findings suggest that spinal neuronal miR-124 might be a potential target for EA effect, and we provide, to our knowledge, a new experimental basis for EA prevention of CIPN.
引用
收藏
页码:410 / 420
页数:12
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