Department of Acu-mox and Tuina, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai 200233, China.
Department of Acu-mox and Tuina, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai 200233, China.
Biomed Pharmacother. 2017 May;89:1125-1135. doi: 10.1016/j.biopha.2017.02.077. Epub 2017 Mar 12.
Electro-acupuncture (EA) has been proven to contribute towards neurologic and functional recoveries in spinal cord injury (SCI), but the underlying mechanism remains largely unknown especially regarding the effects of preventing neuronal apoptosis and alleviating neuropathic pain involved in the development of EA. In this study, we evaluated the effect of EA treatment in an animal model of SCI using the Basso, Beattie, and Bresnahan (BBB) score method, lesion volume by cresyl violet staining and neuronal apoptosis by TUNEL staining. Our results showed that EA therapy improved functional recovery, and reduced tissue loss and neuronal apoptosis after SCI. Meanwhile, we found that proapoptotic proteins (cleaved-caspase-3, 9 and cleaved-PARP) were downregulated and antiapoptotic protein Bcl-2 was upregulated following EA. To further explore the antiapoptotic effect of EA treatment, we verified that a large set of microRNAs (miRNAs) expression were altered following EA treatment and the miR-214 was one of the miRNAs being most significantly upregulated. Importantly, we validated both apoptosis related protein Bax and pain related protein Nav1.3 as two functional targets of miR-214 in vitro and vivo. Furthermore, our data showed that EA attenuates SCI-induced Nav1.3 and Bax upregulation in injured spinal cord via upregulating miR-214. These results suggest that miR-214 played an important role after SCI in the process of EA therapy, and the miR-214 could become an attractive novel therapeutic target for the treatment of SCI.
电针(EA)已被证明有助于脊髓损伤(SCI)中的神经和功能恢复,但潜在机制在很大程度上仍然未知,特别是关于预防神经元凋亡和缓解参与 EA 发展的神经病理性疼痛的作用。在这项研究中,我们使用 Basso、Beattie 和 Bresnahan(BBB)评分法、甲苯胺蓝染色测量损伤体积和 TUNEL 染色检测神经元凋亡,评估了 SCI 动物模型中 EA 治疗的效果。我们的结果表明,EA 治疗可改善 SCI 后的功能恢复,并减少组织损失和神经元凋亡。同时,我们发现 EA 后促凋亡蛋白(裂解 caspase-3、9 和裂解 PARP)下调,抗凋亡蛋白 Bcl-2 上调。为了进一步探讨 EA 治疗的抗凋亡作用,我们验证了 EA 治疗后一组大量 microRNAs(miRNAs)的表达发生改变,其中 miR-214 是上调最显著的 miRNA 之一。重要的是,我们在体外和体内验证了凋亡相关蛋白 Bax 和疼痛相关蛋白 Nav1.3 是 miR-214 的两个功能靶点。此外,我们的数据表明,EA 通过上调 miR-214 来减轻 SCI 诱导的损伤脊髓中 Nav1.3 和 Bax 的上调。这些结果表明,miR-214 在 SCI 后 EA 治疗过程中发挥重要作用,miR-214 可能成为治疗 SCI 的有吸引力的新型治疗靶点。