首都医科大学学报 ›› 2015, Vol. 36 ›› Issue (2): 255-261.doi: 10.3969/j.issn.1006-7795.2015.02.017

• 基础研究 • 上一篇    下一篇

纹状体注射不同剂量6-OHDA制备帕金森病小鼠模型的评价

于燕, 王可, 贾军, 王晓民   

  1. 首都医科大学基础医学院神经生物学系 教育部神经变性病重点实验室 北京市脑重大疾病研究院, 北京 100069
  • 收稿日期:2015-01-20 发布日期:2015-04-16
  • 通讯作者: 王晓民 E-mail:xmwang@ccmu.edu.cn
  • 基金资助:
    国家自然科学基金(81473770,31401024),中国博士后基金(2014M561007)。

Establishment and evaluation of the striatal 6-OHDA lesioned mice model of Parkinson's disease

Yu Yan, Wang Ke, Jia Jun, Wang Xiaomin   

  1. Department of Neurobiology, School of Basic Medical Sciences, Key Laboratory for Neurodegenerative Disorder, Ministry of Education; Beijing Institute for Brain Disorders, Beijing 100069, China
  • Received:2015-01-20 Published:2015-04-16
  • Supported by:
    This study was supported by National Natural Science Foundation of China(81473770, 31401024), Postdoctoral Science Foundation of China(2014M561007).

摘要: 目的 纹状体内注射6-OHDA可用于制备帕金森病(Parkinson's disease,PD)模型,其在小鼠模型上的行为学、形态学及多巴胺水平的变化需要进行系统评价。方法 在小鼠右侧纹状体背外侧部立体定位分别注入4、6、8及10 μg的6羟基多巴胺(6-hydroxydopamine,6-OHDA),动态观察各剂量组小鼠的基本生理状况。旋转行为和转棒行为可评价PD小鼠的运动症状; 酪氨酸羟化酶(tyrosine hydroxylase,TH)免疫组化染色可反映黑质-纹状体内多巴胺能系统的功能改变;高效液相色谱法能检测多巴胺(dopamine,DA)及其代谢产物的含量并分析DA代谢率。结果 除了10 μg 6-OHDA组的小鼠体质量呈一过性下降,其他剂量对小鼠体质量无显著影响。在6-OHDA注射一周后,各组小鼠均出现了持续性的异常旋转行为增加。此外,高剂量组(8 μg及10 μg)小鼠的转棒时间较低剂量组(4 μg及6 μg)小鼠明显缩短。TH组织化学染色显示,低剂量组小鼠损伤侧丢失了约60%的多巴胺神经元及40%的多巴胺神经纤维;而高剂量组小鼠则有超过80%的多巴胺神经元丢失和70%的多巴胺神经纤维减少。各组小鼠损伤侧纹状体内的DA水平及其代谢产物含量也显著降低,与6-OHDA注射量具有剂量依赖性;而DA代谢率却出现了代偿性增加改变。结论 纹状体内注射不同剂量6-OHDA均能引起一定程度的PD病理表型,其损伤程度与6-OHDA剂量相关,为研究PD不同病理阶段及其干预策略提供了新的模型。

关键词: 6-羟基多巴胺, 纹状体, 帕金森病, 小鼠模型

Abstract: Objective To establish different 6-hydroxydopamine(6-OHDA) lesioned mice model, we evaluated the behavioral, neurochemical and histological effect of different dosage injection of 6-OHDA on motor dysfunction and dopamine denervation. Methods Different doses of 6-OHDA(4 μg, 6 μg, 8 μg, 10 μg) were injected into the right dorsal striatum under the facilitation of stereotactic equipment. The body weight after 6-OHDA injection was observed. Apomorphine-induced rotation and rota-rod test were used to estimate motor impairment. Tyrosine hydroxylase(TH) immunostaining was performed to determine the dopaminergic cell loss. Dopamine(DA) content was determined by HPLC. Results 10 μg 6-OHDA injection induced a temporary weight loss, while as other dose of 6-OHDA had no obvious effect on the body weight of mice. At the 1st week after the injection of 6-OHDA, the positive apomorphine induced rotation was observed and this rotational performance was stable for at least 5 weeks. The mice of 8 μg and 10 μg 6-OHDA injection decreased the latency time on the rota-rod. TH-immunolabeling indicated that the 4 μg and 6 μg 6-OHDA injections reduced the number of 60% DA neurons and 40% fibers, as well as 8 μg and 10 μg 6-OHDA injections reduced the number of 80% DA neurons and 70% fibers. Besides, 6-OHDA injection leads to the significant decrease of striatal DA and its metabolites. The decreased of DA content showed a positive correlation with the injection dosage of 6-OHDA, and a negative correlation with dopamine availability(DOPAC+HVA/DA). Conclusion 4 μg and 6 μg 6-OHDA injection induced partial lesions of the nigrostriatal DA system to mimic the early phases of Parkinson's disease(PD). 8 μg and 10 μg 6-OHDA injection induced completely lesions of the nigrostriatal DA system to mimic the late phases of PD.

Key words: 6-hydroxydopamine, striatum, Parkinson's disease, mice model

中图分类号: