中国神经再生研究(英文版) ›› 2019, Vol. 14 ›› Issue (4): 673-682.doi: 10.4103/1673-5374.247471

• 原著:颅神经损伤修复保护与再生 • 上一篇    下一篇

电针促进面神经损伤后的再生:上调神经元胶质细胞源性神经营养因子和神经钙粘素的表达

  

  • 出版日期:2019-04-15 发布日期:2019-04-15

Electroacupuncture promotes peripheral nerve regeneration after facial nerve crush injury and upregulates the expression of glial cell-derived neurotrophic factor

Jing Fei 1 , Lin Gao 1 , Huan-Huan Li 2 , Qiong-Lan Yuan 2 , Lei-Ji Li 1   

  1. 1 Department of Otorhinolaryngology, Head and Neck Surgery, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan Province, China
    2 Department of Anatomy and Neurobiology, Tongji University School of Medicine, Shanghai, China
  • Online:2019-04-15 Published:2019-04-15
  • Contact: Lei-Ji Li, MD, 83193604@qq.com.

摘要:

电针疗法治疗周围性面瘫的疗效确切,但具体机制一直不明确。以往有研究表明,作为胶质细胞源性神经营养因子通过与N-钙粘素结合可保护神经元。课题组以往的研究也表明,电针能上调神面经元中的N-钙粘素mRNA表达,从而促进面神经再生。故本次实验以此为点,旨在验证观察胶质细胞源性神经营养因子和神经钙粘素在周围面神经压榨性损伤后对中枢面神经元的作用,探讨电针促进面神经再生的可能机制。将111只新西兰大白兔随机分成正常组21只,不做任何处理和治疗,损伤组45只,制作右侧面神经上颊支压榨性损伤的面神经损伤模型,电针组45只,造模后即进行右侧“翳风(TE17)”、“颊车(ST6)”、“四白(ST2)”、“地仓(ST4)”、“阳白(GB14)”、“颧髎(SI18)” 穴位电针刺及“合谷(L14)”埋针治疗。(1)行为学评分检测显示:术后14 d,电针组行为学眨眼反射、触须运动、鼻尖位置评分总分明显低于损伤组,说明电针能显著促进面肌功能的恢复;(2)各组脑桥中下部含面神经元的脑干组织苏木精伊红染色及尼氏染色结果显示:术后7 d,电针组凋亡神经元数量明显少于损伤组,且术后21 d,电针组与正常组神经元数目无显著差异;(3)各组右侧颊肌组织苏木精伊红染色显示:电针组横截面积在术后1,14,21 d大于损伤组;(4)各组右侧面神经组织甲苯胺蓝染色显示:术后14 d,与损伤组相比,电针组神经轴突脱髓鞘反应减轻,炎性细胞减少;(5)qRT-PCR结果显示,与损伤组相比,电针组术后4,7,14,21 d面神经元组织神经钙粘素 mRNA表达及术后4,7,14 d 胶质细胞源性神经营养因子 mRNA表达均明显升高;(6)Western blot结果显示:与损伤组相比,电针在术后4,7,14 d能明显上调面神经元N-cadherin蛋白的表达,在术后7,14,21 d明显上调面神经元胶质细胞源性神经营养因子蛋白的表达;(7)上述数据说明,电针促进兔面神经外周部压榨性损伤后的再生,抑制神经元凋亡并减轻外周炎性反应,其机制是通过上调胶质细胞源性神经营养因子和N-cadherin在中枢面神经元中的表达而实现。

orcid: 0000-0002-9531-7400(Lei-Ji Li)

关键词: 周围性面瘫, 电针, GDNF, N-cadherin, 压榨损伤, 神经再生, 神经元再生, 神经元凋亡, 面神经元, 神经脱髓鞘

Abstract:

The efficacy of electroacupuncture in the treatment of peripheral facial paralysis is known, but the specific mechanism has not been clar¬ified. Glial cell-derived neurotrophic factor (GDNF) has been shown to protect neurons by binding to N-cadherin. Our previous results have shown that electroacupuncture could increase the expression of N-cadherin mRNA in facial neurons and promote facial nerve re¬generation. In this study, the potential mechanisms by which electroacupuncture promotes nerve regeneration were elucidated through assessing the effects of electroacupuncture on GDNF and N-cadherin expression in facial motoneurons of rabbits with peripheral facial nerve crush injury. New Zealand rabbits were randomly divided into a normal group (normal control, n = 21), injury group (n = 45) and electroacupuncture group (n = 45). Model rabbits underwent facial nerve crush injury only. Rabbits in the electroacupuncture group received facial nerve injury, and then underwent electroacupuncture at Yifeng (TE17), Jiache (ST6), Sibai (ST2), Dicang (ST4), Yangbai (GB14), Quanliao (SI18), and Hegu (LI4; only acupuncture, no electrical stimulation). The results showed that in behavioral assessments, the total scores of blink reflex, vibrissae movement, and position of apex nasi, were markedly lower in the EA group than those in the injury group. Hematoxylin-eosin staining of the right buccinator muscle of each group showed that the cross-sectional area of buccinator was larger in the electroacupuncture group than in the injury group on days 1, 14 and 21 post-surgery. Toluidine blue staining of the right facial nerve tissue of each group revealed that on day 14 post-surgery, there was less axonal demyelination and fewer inflammatory cells in the electroacupuncture group compared with the injury group. Quantitative real time-polymerase chain reaction showed that compared with the injury group, N-cadherin mRNA levels on days 4, 7, 14 and 21 and GDNF mRNA levels on days 4, 7 and 14 were significant¬ly higher in the electroacupuncture group. Western blot assay displayed that compared with the injury group, the expression of GDNF protein levels on days 7, 14 and 21 were significantly upregulated in the electroacupuncture group. The histology with hematoxylin-eosin staining and Nissl staining of brainstem tissues containing facial neurons in the middle and lower part of the pons exhibited that on day 7 post-surgery, there were significantly fewer apoptotic neurons in the electroacupuncture group than in the injury group. By day 21, there was no significantly difference in the number of neurons between the electroacupuncture and normal groups. Taken together, these results have confirmed that electroacupuncture promotes regeneration of peripheral facial nerve injury in rabbits, inhibits neuronal apoptosis, and reduces peripheral inflammatory response, resulting in the recovery of facial muscle function. This is achieved by up-regulating the expression of GDNF and N-cadherin in central facial neurons.

Key words: nerve regeneration, facial paralysis, electroacupuncture, glial cell-derived neurotrophic factor, N-cadherin, crush injury, neuronal apoptosis, facial neuron, nerve demyelination, neural regeneration