喉返神经损伤后神经肌肉变化及再生特点研究

白玉, 徐文, 胡蓉, 等. 喉返神经损伤后神经肌肉变化及再生特点研究[J]. 临床耳鼻咽喉头颈外科杂志, 2017, 31(12): 932-936. doi: 10.13201/j.issn.1001-1781.2017.12.009
引用本文: 白玉, 徐文, 胡蓉, 等. 喉返神经损伤后神经肌肉变化及再生特点研究[J]. 临床耳鼻咽喉头颈外科杂志, 2017, 31(12): 932-936. doi: 10.13201/j.issn.1001-1781.2017.12.009
BAI Yu, XU Wen, HU Rong, et al. Degeneration and regeneration characteristics of nerves and muscles after recurrent laryngeal nerve injury[J]. J Clin Otorhinolaryngol Head Neck Surg, 2017, 31(12): 932-936. doi: 10.13201/j.issn.1001-1781.2017.12.009
Citation: BAI Yu, XU Wen, HU Rong, et al. Degeneration and regeneration characteristics of nerves and muscles after recurrent laryngeal nerve injury[J]. J Clin Otorhinolaryngol Head Neck Surg, 2017, 31(12): 932-936. doi: 10.13201/j.issn.1001-1781.2017.12.009

喉返神经损伤后神经肌肉变化及再生特点研究

  • 基金项目:

    国家自然科学基金 (No:81170901)

    北京市自然科学基金 (No:7132053)

详细信息
    通讯作者: 徐文,E-mail:entwen@trohs.com
  • 中图分类号: R767

Degeneration and regeneration characteristics of nerves and muscles after recurrent laryngeal nerve injury

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  • 目的:观察大鼠喉返神经不同程度损伤后神经及甲杓肌变化、再生特点及其相互关系。方法:实验用SD大鼠95只,因感染死亡2只、手术死亡2只、运输途中死亡1只未计入统计外,将剩余90只大鼠分为完全损伤组(横断伤)及不完全损伤组(钳夹伤)各43例,对照组4例。造模成功后6 h、12 h、1 d、3 d、5 d、1周、2周、3周及4周观察喉运动情况,甲杓肌肌电生理及病理组织学特点,喉返神经病理形态及超微结构变化特征。结果:大鼠喉返神经损伤后均即刻出现声带固定。完全损伤组未见声带活动恢复;不完全损伤组中41例于伤后2周声带活动恢复正常,另2例分别于伤后3周及4周声带活动恢复正常。完全损伤组伤后1 d甲杓肌出现纤颤波,伤后4周出现神经再生电位;不完全损伤组甲杓肌于伤后2周内可观察到失神经电位,3周后肌电恢复正常。两组甲杓肌伤后4周均出现肌细胞卷曲变性、横纹溶解等失神经表现,完全损伤组随时间的延长肌萎缩逐渐加重,不完全损伤组损伤2周后肌萎缩现象开始逐渐好转。完全损伤组喉返神经损伤后,神经远端崩解变性程度较近端明显,伤后4周出现少量粗大的有髓神经纤维;不完全损伤组伤后1 d有髓神经破坏最明显,随后逐渐好转,至伤后1周基本正常。完全损伤组Schwann细胞于伤后2周内出现吞噬现象,3周后开始出现不包绕神经纤维的Schwann细胞,以近端尤为明显;不完全损伤组伤后1周内可见Schwann吞噬现象,偶见凋亡及变性。炎性反应在完全损伤组更为严重,同时纤维母细胞及成纤维细胞逐渐增多,间质中胶原成分增加。结论:喉返神经完全损伤后,神经远端变性更为明显,伤后4周观察到再生神经,不完全损伤的喉返神经具有自我修复能力,结构恢复早于神经功能的恢复。Schwann细胞伤后可发挥吞噬作用,并有幼稚型出现。神经纤维崩解产物可能不是诱导巨噬细胞产生趋化作用的原因,但却加速巨噬细胞的迁移活化。
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  • [1]

    XU W, HAN D, HOU L, et al.Clinical and electrophysiological characteristics of larynx in myasthenia gravis[J].Ann Otol Rhinol Laryngol, 2009, 118:656-661.

    [2]

    徐文, 赵功伟, 胡慧英, 等.喉返神经损伤后喉肌病理生理研究[J].临床耳鼻咽喉头颈外科杂志, 2009, 23 (9):403-406.

    [3]

    ALLODI I, UDINA E, NAVARRO X.Specificity of peripheral nerve regeneration:interactions at the axon level[J].Prog Neurobiol, 2012, 98:16-37.

    [4]

    JESSEN K R, MIRSKY R.Negative regulation of myelination:relevance for development, injury, and demyelinating disease[J].Glia, 2008, 56:1552-1565.

    [5]

    TAKADA H, YUASA S, ARAKI T.Demyelination can proceed independently of axonal degradation during Wallerian degeneration in wlds mice[J].Eur J Neurosci, 2011, 34:531-537.

    [6]

    BEIROWSKI B, BABETTO E, COLEMAN M P, et al.The WldS gene delays axonal but not somatic degeneration in a rat glaucoma model[J].Eur J Neurosci, 2008, 28:1166-1179.

    [7]

    PITMAN M J, WEISSBROD P, ROARK R, et al.Electromyographic and histologic evolution of the recurrent laryngeal nerve from transection and anastomosis to mature reinnervation[J].Laryngoscope, 2011, 121:325-331.

    [8]

    HADLOCK T A, KOWALESKI J, LO D, et al.Rodent facial nerve recovery after selected lesions and repair technique[J].Plast Reconstr Surg, 2010, 125:99-109.

    [9]

    MARTINI R, FISCHER S, LPEZ-VALES R, et al.Interactions between Schwann cells and macrophages in injury and inherited demyelinating disease[J].Glia, 2008, 56:1566-1577.

    [10]

    STOLL G, GRIFFIN J W, LI C Y, et al.Wallerian degeneration in the peripheral nervous system:participation of both Schwann cells and macrophages in myelin degradation[J].J Neurocytol, 1989, 18:671-683.

    [11]

    付秀美, 王荣良, 杨振江, 等.施万样细胞对大鼠脊神经节NGF和BDNF表达的影响[J].中国临床解剖学杂志, 2017, 35 (1):48-51.

    [12]

    INO D, SAGARA H, SUZUKI J, et al.Neuronal Regulation of Schwann Cell Mitochondrial Ca (2+) Signaling during Myelination[J].Cell Rep, 2015, 12:1951-1959.

    [13]

    MIRSKY R, JESSEN K R, BRENNAN A, et al.Schwann cells as regulators of nerve development[J].J Physiol Paris, 2002, 96:17-24.

    [14]

    HKE A, CHENG C, ZOCHODNE D W.Expression of glial cell line-derived neurotrophic factor family of growth factors inperipheral nerve injury in rats[J].Neuroreport, 2000, 11:1651-1654.

    [15]

    TAKAGI T, ISHII K, SHIBATA S, et al.Schwannspheres derived from injured peripheral nerves in adult mice-their in vitro characterization and therapeutic potential[J].PLoS One, 2011, 6:e21497.

    [16]

    ROSENBERG A F, WOLMAN M A, FRANZINIARMSTRONG C, et al.In vivo nerve-macrophage interactions following peripheral nerve injury[J].J Neurosci, 2012, 32:3898-3909.

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出版历程
收稿日期:  2017-03-27

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