Literature DB >> 29513163

Electrical stimulation promotes regeneration and re-myelination of axons of injured facial nerve in rats.

Yue Deng1, Yaping Xu1, Huanhai Liu1, Hu Peng1, Qilei Tao1, Hongyi Liu1, Haibin Liu1, Jian Wu1, Xiaoping Chen2, Jingping Fan1.   

Abstract

Objective To investigate the effects of electrical stimulation (ES) on the nerve regeneration and functional recovery of facial expression muscles in facial nerve defect rats. Methods Sixty rats were surgically introduced with a 1-cm defect on the right facial nerves and evenly divided into the Surgery group (Group A, the main trunk of the right facial nerve was surgically cut-off with a 1.0 cm at the foramina stylomastoideum) and the Surgery + ES group (Group B). Twenty normal rats were as normal control group (without receiving surgery or ES). For rats in group B, the orbicularis oris muscle of the right paralyzed face was stimulated with an electrical pulse of 3 V, 20 Hz and 0.3 mA for 1 h each day. The effects of ES on the facial muscle movement, compound muscle action potentials (CMAPs), histological structure, and the expression levels of S100B and NF200 proteins were comparatively studied. Results In group A, facial paralysis scores were slightly improved from day 1 to 28; the facial nerve trunks had swelled and malformed till day 14; and CMAPs could be induced in fewer animals and were abnormal, resulting in a slow recovery of the facial muscle movement. In group B, facial paralysis scores were improved from 4 to 2.6 during the 4 weeks; more rats showed a higher amplitude and shorter latency of CMAPs from day 14 to 28 after surgery; and increased axons and the expression of S100B and NF200 proteins and gradually decreased swelling in the injured facial nerve. Conclusion ES promotes outgrowth and myelination of axons and a partial functional recovery of facial muscles in injured facial nerve rats.

Entities:  

Keywords:  Electrical stimulation; facial paralysis scores; injured facial nerve; regeneration and re-myelination of axons

Mesh:

Substances:

Year:  2018        PMID: 29513163     DOI: 10.1080/01616412.2018.1428390

Source DB:  PubMed          Journal:  Neurol Res        ISSN: 0161-6412            Impact factor:   2.448


  6 in total

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Authors:  Brian M Balog; Kangli Deng; Vinod Labhasetwar; Kathryn J Jones; Margot S Damaser
Journal:  Curr Opin Urol       Date:  2019-07       Impact factor: 2.309

2.  Facial nerve repair utilizing intraoperative repair strategies.

Authors:  Brandon L Brown; Morgan M Sandelski; Sarah M Drejet; Elizabeth M Runge; Taha Z Shipchandler; Kathryn J Jones; Chandler L Walker
Journal:  Laryngoscope Investig Otolaryngol       Date:  2020-05-28

3.  A fully biodegradable and self-electrified device for neuroregenerative medicine.

Authors:  Liu Wang; Changfeng Lu; Shuhui Yang; Pengcheng Sun; Yu Wang; Yanjun Guan; Shuang Liu; Dali Cheng; Haoye Meng; Qiang Wang; Jianguo He; Hanqing Hou; Huo Li; Wei Lu; Yanxu Zhao; Jing Wang; Yaqiong Zhu; Yunxuan Li; Dong Luo; Tong Li; Hao Chen; Shirong Wang; Xing Sheng; Wei Xiong; Xiumei Wang; Jiang Peng; Lan Yin
Journal:  Sci Adv       Date:  2020-12-11       Impact factor: 14.136

4.  The effect of charge-balanced transcutaneous electrical nerve stimulation on rodent facial nerve regeneration.

Authors:  Young Sang Cho; Onjeon Ryu; Kyeongwon Cho; Dohyoung Kim; Jihyun Lim; Sung Hwa Hong; Yang-Sun Cho
Journal:  Sci Rep       Date:  2022-01-26       Impact factor: 4.379

Review 5.  3D Printed Personalized Nerve Guide Conduits for Precision Repair of Peripheral Nerve Defects.

Authors:  Kai Liu; Lesan Yan; Ruotao Li; Zhiming Song; Jianxun Ding; Bin Liu; Xuesi Chen
Journal:  Adv Sci (Weinh)       Date:  2022-02-18       Impact factor: 17.521

6.  Electrical stimulation of human neural stem cells via conductive polymer nerve guides enhances peripheral nerve recovery.

Authors:  Shang Song; Kelly W McConnell; Danielle Amores; Alexa Levinson; Hannes Vogel; Marco Quarta; Thomas A Rando; Paul M George
Journal:  Biomaterials       Date:  2021-06-23       Impact factor: 15.304

  6 in total

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