中国神经再生研究(英文版) ›› 2018, Vol. 13 ›› Issue (7): 1276-1280.doi: 10.4103/1673-5374.235076

• 原著:退行性病与再生 • 上一篇    下一篇

鱼藤酮和6-羟多巴胺诱导的帕金森病大鼠模型:大脑病理改变有差异吗?

  

  • 收稿日期:2018-05-26 出版日期:2018-07-15 发布日期:2018-07-15
  • 基金资助:

    秦皇岛市科技支持项目(201402B036);河北省科技项目(1427777118D

Differences in brain pathological changes between rotenone and 6-hydroxydopamine Parkinson’s disease models

Lan-Xiang Liu1, Dan Du1, Zhan-Qiu Wang1, Yuan Fang1, Tao Zheng1, Yan-Chao Dong2, Qing-Lei Shi3, Min Zhao4, Fang Xiao4, Juan Du5   

  1. 1 Department of Magnetic Resonance Imaging, Qinhuangdao Municipal No. 1 Hospital, Qinhuangdao, Hebei Province, China
    2 Department of Intervention, Qinhuangdao Municipal No. 1 Hospital, Qinhuangdao, Hebei Province, China
    3 Siemens Ltd., Beijing, China
    4 Department of Pathology, Qinhuangdao Municipal No. 1 Hospital, Qinhuangdao, Hebei Province, China
    5 Hebei Medical University, Shijiazhuang, Hebei Province, China
  • Received:2018-05-26 Online:2018-07-15 Published:2018-07-15
  • Contact: Lan-Xiang Liu,liulanxiang66@sina.com
  • Supported by:

    This study was supported by a grant from the Qinhuangdao Science-Technology Support Project of China, No. 201402B036; a grant from the Science and Technology Project of Hebei Province of China, No. 1427777118D

摘要:

 

鱼藤酮和6-羟多巴胺诱导帕金森动物模型常用的2种药物,它们不仅能够实现黑质多巴胺神经元退行性改变,还能满足研究中对铁沉积的要求,但比较这2种模型在磁共振成像及测量方面各自有何特点,则少有研究,实验你探讨此问题。设计方案为分别在右侧黑质注射3 µg鱼藤酮或10 μg 6-羟多巴胺诱导帕金森病大鼠模型,注射后1,2,4,6周时MRI进行冠状全脑T2加权成像、横向全脑T2加权成像和冠状扩散张量加权成像,计算损伤部位分数各向异性和T2*值。见鱼藤酮诱导模型大鼠大脑黑质右侧分数各向异性值在第6周时明显低于其他时间点,6-羟多巴胺诱导模型大鼠大脑黑质右侧分数各向异性值降低,第1周时分数各向异性值和T2*值升高。提示6-羟多巴胺诱导的大鼠模型似乎更适合短时间研究多巴胺能神经元,而鱼藤酮诱导的大鼠模型可能更适合于研究帕金森病的远期病理和生理过程。

orcid:0000-0002-7434-4434(Lan-Xiang Liu)

关键词: 分数各向异性, T2*, 鱼藤酮, 6-羟多巴胺, 帕金森病, MRI, 扩散张量成像, 多巴胺能神经元, 神经再生

Abstract:

Rotenone and 6-hydroxydopamine are two drugs commonly used to generate Parkinson’s disease animal models. They not only achieve degenerative changes of dopaminergic neurons in the substantia nigra, but also satisfy the requirements for iron deposition. However, few studies have compared the characteristics of these two models by magnetic resonance imaging. In this study, rat models of Parkinson’s disease were generated by injection of 3 μg rotenone or 10 μg 6-hydroxydopamine into the right substantia nigra. At 1, 2, 4, and 6 weeks after injection, coronal whole-brain T2-weighted imaging, transverse whole-brain T2-weighted imaging, and coronal diffusion tensor weighted imaging were conducted to measure fractional anisotropy and T2* values at the injury site. The fractional anisotropy value on the right side of the substantia nigra was remarkably lower at 6 weeks than at other time points in the rotenone group. In the 6-hydroxydopamine group,the fractional anisotropy value was decreased, but T2* values were increased on the right side of the substantia nigra at 1 week. Our findings confirm that the 6-hydroxydopamine-induced model is suitable for studying dopaminergic neurons over short periods, while the rotenone-induced model may be appropriate for studying the pathological and physiological processes of Parkinson’s disease over long periods.

Key words: nerve regeneration, fractional anisotropy, T2*, rotenone, 6-hydroxydopamine, Parkinson’s disease, magnetic resonance imaging, diffusion tensor imaging, dopaminergic neurons, neural regeneration