首页> 外文期刊>Biomedicine & pharmacotherapy =: Biomedecine & pharmacotherapie >Electro-acupuncture-modulated miR-214 prevents neuronal apoptosis by targeting Bax and inhibits sodium channel Nav1.3 expression in rats after spinal cord injury
【24h】

Electro-acupuncture-modulated miR-214 prevents neuronal apoptosis by targeting Bax and inhibits sodium channel Nav1.3 expression in rats after spinal cord injury

机译:电针调制的miR-214通过靶向诱导抗体来防止神经元细胞凋亡,并抑制脊髓损伤后大鼠的钠通道Nav1.3表达

获取原文
获取原文并翻译 | 示例
           

摘要

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. (C) 2017 Elsevier Masson SAS. All rights reserved.
机译:被证明的电针(EA)已被证明有助于脊髓损伤(SCI)中的神经系统和功能性质,但潜在机制仍然很大程度上未知,特别是预防神经元细胞凋亡的影响,并减轻ea发展中涉及的神经性疼痛。在本研究中,我们评估了使用贝索,Beattie和Bresnahan(BBB)评分法,枸杞染色和神经细胞凋亡的病变体积对SCI动物模型中EA治疗的影响。我们的研究结果表明,EA治疗改善了功能恢复,并在SCI后减少了组织丧失和神经元凋亡。同时,我们发现促凋亡蛋白(切割 - caspase-3,9和切割PARP)被下调,并且在EA之后上调抗曝气蛋白Bcl-2。为了进一步探索EA治疗的抗污染效果,我们验证了在EA治疗后改变了大量的MicroRNA(miRNA)表达,并且miR-214是最显着上调的miRNA之一。重要的是,我们将凋亡相关的蛋白质Bax和疼痛相关蛋白质Nav1.3验证为miR-214体外和体内的两个功能靶标。此外,我们的数据显示EA通过上调miR-214衰减受损脊髓中的SCI诱导的Nav1.3和Bax Upregulation。这些结果表明MiR-214在EA治疗过程中SCI后发挥着重要作用,并且MIR-214可以成为治疗SCI的有吸引力的新疗法靶标。 (c)2017年Elsevier Masson SAS。版权所有。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号