小胶质细胞
外围设备
医学
周围神经病变
电针
神经科学
免疫学
炎症
内科学
病理
内分泌学
针灸科
生物
替代医学
糖尿病
作者
Xiaochen Li,Yinghui Hua,Yu Chen,Yu‐Xia Chu,Wen-Li Mi,Yanqing Wang,Qi‐Liang Mao‐Ying
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2023-12-13
卷期号:212 (3): 410-420
被引量:2
标识
DOI:10.4049/jimmunol.2300539
摘要
Abstract 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 adeno-associated 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.
科研通智能强力驱动
Strongly Powered by AbleSci AI