期刊文献+

6-OHDA制作帕金森病大鼠模型及评估 被引量:11

Establishment and Evaluation of Parkinson's disease model of rat with 6-OHDA
下载PDF
导出
摘要 目的应用6-OHDA制作帕金森病(PD)大鼠模型,并对不同剂量6-OHDA制作的模型进行综合评价。方法取雄性SD大鼠70只,随机分成12μl单点、8μl单点、4μl单点、8μl双点和对照组,采用立体定向法,分别行左侧纹状体区相应剂量6-OHDA单点及双点注射,检测大鼠行为学变化及黑质多巴胺(DA)能神经元变化。结果双点组大鼠模型病死率高于其余各组,12μl单点组大鼠模型成功率高于其余各组,行为学检测见各单点组随6-OHDA剂量增加,其异常行为出现率增高;免疫组化检测各单点组间存在显著差异,但12μl单点组与双点组之间无显著差异。结论纹状体区对6-OHDA损伤存在剂量依赖性,12μl单点注射方法优于双点注射法。 Objective The aim of this study is to establish a stable and easy to perform Parkinson's disease rat model by using 6-OHDA.Methods 70 male SD rats were used in this study. Different doses(4μl,8μl,12μl) of 6-OHDA were injected to the left striaturn area by employing single-injection strategy under the facilitation of stereotaxis equiprnents.8gl of 6-OHDA was injected by employing double-position injection strategy to act as a postitive control grop. The control group was injected with the same volume of saline. The ethological alterations and the suhsbstantia nigra dopaminergic neuronal changes were investigated to compare the profiles of PD models induced by different doses and by single or double-position injection methods of 6-OHDA at the dosage of 8μl.Results The motality rate of rats employing double-position strategy was higher that other groups. The 12μl group rats showed increased successful model rates in comparision with other groups' rats. No significant ethological changes were in either groups. Conclusion In this study a stable and easy to perform PD rat model was established successfully by employing single-position injection strategy of 6-OHDA at adose of 12μl to stria- turn area.This study builds a strong experimental and theoretical basis on making PD animal models with better successful rate and less mortality rate and will facilitate the further research on PD.
作者 张伟 杨辉
出处 《四川医学》 CAS 2007年第8期818-820,共3页 Sichuan Medical Journal
基金 国家自然科学基金资助项目(No.30371461)
关键词 帕金森病 大鼠模型 6-羟基多巴胺 纹状体 Parkinson's disease(PD) rat model 6-OHDA corpora striatum(CS)
  • 相关文献

参考文献10

二级参考文献43

  • 1周嘉伟,武义鸣,徐慧君,冯家笙.帕金森病大白鼠动物模型的建立[J].南通医学院学报,1989,9(2):84-86. 被引量:13
  • 2周明付,张华,吴金良,郭漳生,林玲,汤善钧,周祥庭.大鼠帕金森氏病模型的建立[J].河南医科大学学报,1994,29(4):289-292. 被引量:14
  • 3邵宴平 焦守恕 等.脑细胞悬液移植治疗黑质损伤-1.黑质损伤动物模型的建立[J].北京第二医学院学报,1986,7:107-107. 被引量:5
  • 4包新民 舒斯之.大鼠脑立体定向图谱[M].北京:人民卫生出版社,1991.39-40. 被引量:27
  • 5Mattson MP. Metal - catalyzed disruption of membrance protein and lipid signaling in the pathogenesis of neurodegenerative disorder. Ann N Y Acad Sci, 2004; 1012:37~50. 被引量:1
  • 6Tsang F, Soong TW. Interaction between environmental and genetic factors in the pathophysiology of Parkinson's disease. HUBMB Life, 2003; 55 (6): 323~327. 被引量:1
  • 7Bush AI. Metal and neuroscience. Curr Opin Chem Biol,2000; 4 (2): 184~191. 被引量:1
  • 8Sayre LM, Perry G, Atwood GS et al. The role of metals in neurodegenerative disease. Cell Mol Bio, 2000; 46(4): 731~741. 被引量:1
  • 9Sadryadeh SM, Saffari Y. Iron and brain disorders. Am J ClinPathol, 2004; 121 (Suppl): S64~67. 被引量:1
  • 10Levenson CW. Iron and Parkinson's disease: chelator to the recuse? Nutr Rev, 2003; 61 (9): 311~313. 被引量:1

共引文献51

同被引文献91

引证文献11

二级引证文献34

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部