首页 | 本学科首页   官方微博 | 高级检索  
     

家兔迟发性面瘫模型建立及药物干预研究
引用本文:吴政海洪文瑶管宏新郑学胜王旭辉李心远李世亭. 家兔迟发性面瘫模型建立及药物干预研究[J]. 现代生物医学进展, 2011, 11(11): 2113-2116
作者姓名:吴政海洪文瑶管宏新郑学胜王旭辉李心远李世亭
作者单位:上海交通大学医学院附属新华医院神经外科,上海交通大学颅神经疾病诊治中心,上海,200092
摘    要:目的:优化迟发性面瘫的建模方法,并对药物的神经保护作用进行观察。方法:家兔48只共96侧面神经,分A、B、C、D 4个实验组,以一侧面神经进行实验处理,另一侧为自身对照。A组:直视下钳夹损伤桥池段面神经;B组:直视下向桥小脑角注射动脉血,以诱导血管痉挛;C组:处理因素=A组+B组;D组:在C组基础上,应用药物(强的松+丹参+维生素B1+维生素B12)干预。观察家兔面瘫,并做面神经病理切片,比较各组间迟发性面瘫发生率、面瘫持续时间及预后。结果:面瘫发生情况:A组6只家兔(6/11,54.5%)出现迟发性面瘫;平均面瘫持续时间为13.2天。B组有2只(2/12,16.7%)出现迟发性面瘫,平均持续8天。C组6只(6/12,50%)家兔出现迟发性面瘫,平均持续14.3天。D组4只(4/12,33.33%)出现迟发性面瘫,平均持续6天。所有自身对照侧均无面瘫发生。病理:各组均见神经纤维水肿;A、C两组呈高度水肿改变,神经束周围结构紊乱;B组见神经内血管细小,而水肿较A、C两组轻微;D组呈轻度水肿改变。结论:C组出现迟发性面瘫几率高,是较好的模型;联合应用强的松、丹参、维生素B1、维生素B12虽不能防止迟发性面瘫发生,但可使迟发性面瘫病程明显缩短。

关 键 词:迟发性面瘫  模型  药物防治

Rabbit Model of Delayed Facial Paralysis and Drug Intervention
WU Zheng-hai,HONG Wen-yao,GUAN Hong-xin,ZHENG Xue-sheng,WANG Xu-hui,LI Xin-yuan,LI Shi-ting. Rabbit Model of Delayed Facial Paralysis and Drug Intervention[J]. Progress in Modern Biomedicine, 2011, 11(11): 2113-2116
Authors:WU Zheng-hai  HONG Wen-yao  GUAN Hong-xin  ZHENG Xue-sheng  WANG Xu-hui  LI Xin-yuan  LI Shi-ting
Affiliation:△(Department of Neurosurgery,Xinhua Hospital AND cranial nerves Treatment Center,Shanghai Jiao Tong University School of Medicine,Shanghai 200092,China)
Abstract:ABSTRACTObjective:Optimization ofmodeling of delayed facial paralysis.The neuroprotective effect of several drugswere observed.Methods: Forty-eight rabbits were assigned to A, B, C, D 4 experimental groups, with one side of the facial nerve to the experimentaltreatment, and the other side of self-control. A: The cisternal section of the facial nerve was injured by clamp. B: Injection of arterialblood to the cerebellopontine angle to induce vasospasm. C: treatment factor = group A + group B. D group: C group plus the applicationof drug (prednisone + SM + vitamin B1 + vitamin B12) intervention. The rabbit facial paralysis was observed. And facial nerve biopsywas done. The incidence of delayed facial paralysis, duration and prognosis were compared. Results: The incidence of facial paralysis: ingroup A 6 rabbits (6 / 11, 54.5%) had delayed facial paralysis; the average duration of facial paralysis was 13.2 days. In group B, 2 (2 /12, 16.7%) had delayed facial paralysis, the average duration was 8 days. In group C 6 (6 / 12, 50%) had delayed facial paralysis, and theaverage duration was 14.3 days. In group D 4 (4 / 12, 33.33%) had delayed facial paralysis, the average duration was 6 days. There wasno facial paralysis in all self-control sides. Pathology: Nerve fiber edema was seen in each group ; groups A, C showed a high degree ofedema, with nerve bundles around the structural disorder; group B showed small blood vessels within the nerve, and mild edema comparedwith groups A, C; group D showed a slight edema change. Conclusion: Group C had higher risk of delayed facial paralysis, so it isa better model. Combination of prednisone, Salvia, vitamin B1, vitamin B12, although not able to prevent the occurrence of delayed facialparalysis, but the duration of the delayed facial paralysis was significantly shortened.
Keywords:Delayed facial paralysis   Model   Drug prevention and treatment
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《现代生物医学进展》浏览原始摘要信息
点击此处可从《现代生物医学进展》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号