期刊文献+

中药调心方对氧化损伤型类Alzheimer病大鼠线粒体呼吸链酶活性和钙稳态的影响 被引量:3

Effect of HBR on mitochondrial respiratory oxidase and calcium homeostasis of oxidative damaged AD rat model
下载PDF
导出
摘要 目的 观察调心方对氧化损伤型类Alzheimer病 (AD)大鼠线粒体呼吸链酶活性和钙稳态的影响。方法 采用二羟延胡索酸 (DHF) +FeCl3+ADP左侧脑室注射法建立氧化损伤型类AD大鼠模型。Morris水迷宫法观察大鼠空间学习记忆能力 ;Clark氧电极法观察脑皮层线粒体呼吸链氧化酶活性 ;原位杂交法观察脑皮层线粒体细胞色素氧化酶Ⅱ型亚基 (COⅡ )mRNA表达 ;Fura 2 /AM 荧光法测定脑皮层和海马Ca2 + 含量以及调心方对AD大鼠上述各项指标变化的影响。结果 与正常对照组比较 ,AD模型大鼠空间学习记忆能力、脑线粒体细胞色素氧化酶活性和皮层COⅡmRNA表达明显降低 ,皮层和海马神经元内Ca2 + 含量显著增高 ;调心方对上述各项指标有不同程度的改善作用。结论 调心方具有改善AD大鼠空间学习记忆能力、脑线粒体细胞色素氧化酶活性、皮层COⅡmRNA表达和钙稳态失衡的作用。 Objective To observe the effect of the Heart Benefiting Recipe(HBR) on the abilities of spatial learning memory.The activities of oxidase in mitochondrial respiratory and calcium homeostasis etc.in brain of the oxidative damaged AD rat model.Methods The rats were injected with the oxygen free radical generation system (DHF-FeCl 3-ADP) in left ventricles of the brain and induced oxidative damaged AD rat model. The spatial learning memory abilities were observed by Morris water maze test. The activities of cytochrome oxidase(CO) were determined using Clark oxygen electrode method.The expression of COⅡ mRNA was observed by in situ hybridization.The contents of cytoplasm Ca 2+ were determined using Fura2/AM- fluorescence method. The regulating effects of HBR on above indices were also studied.Results Compared with the normal group, the abilities of spatial learning memory, the activities of oxidase in mitochondrial respiratory and the expression of COⅡ mRNA were decreased obviously. The contents of calcium in cytoplasm of cortex and hippocampus were increased significantly.HBR, however, could improve the indexes of above mentioned in varying degrees.Conclusions The data demonstrated that the clinical efficacy of HBR on AD may be partly resulted from its improving the abilities of spatial learning memory, the activities of oxidase in mitochondrial respiratory , the expression of COⅡ mRNA and the calcium homeostasis.
出处 《中国老年学杂志》 CAS CSCD 北大核心 2003年第6期364-366,共3页 Chinese Journal of Gerontology
基金 国家自然科学基金重点项目 (39830 4 50 )
关键词 中药 调心方 氧化损伤型 ALZHEIMER病 大鼠 线粒体 钙稳态 细胞色素氧化酶活性 Alzheimer disease(AD) Cytochrome oxidase Calcium homeostasis Heart benefiting recipe(HBR)
  • 相关文献

参考文献11

  • 1周晖,赵伟康.调心方对βA大鼠痴呆模型空间学习记忆障碍和胆碱能系统的影响[J].中药药理与临床,1998,14(3):29-31. 被引量:29
  • 2林水淼 杨柏灿.补气活血、调心,补肾和化痰开窍改善早老性痴呆的临床研究[J].中药药理与临床研究进展,1996,10:202-210.
  • 3Markesbery WR . Oxidative stress hypothesis in Alzheimer's Disease [J]. Free Radical Biol Med, 1997 ; 23 (1) : 134-147.
  • 4Sugawara H.Tobise K. Kikuchi K. Antioxidant effects of calcium antagonists on rat myocardial membrane lipid peroxidation [J].Hypertens Res,1996;19(4) :223-228.
  • 5Nitta A.β-amyloid protein-induced Alzheimer disease animal model[J]. Neurosci Lett, 1994 ; 179 : 63-66.
  • 6Morris RJ. Developments of a water-maze procedure for studying spatial learning in the rats [J]. Neurosci Methods,1984;11:47-60.
  • 7Heinz S . Liposome-mitochondrial inner membrane fusion [J]. J Biochem, 1980 ; 255(8) : 3748-3756.
  • 8Nancy A. Functional alterations in Alzheimer's disease:Selective loss of mitochondrial-encoded cytochrome oxidase mRNA in the hippocampal formation [J]. J Neuropathol Exp Neurol, 1994, 53(5):508-512.
  • 9Jo Ellen Dildy,Steven W Leslie. Ethanol inhibits NMDA-induced increases in free intracellular Ca2+ in dissociated brain cells [J].Brain Res ,1989;499 : 383-387.
  • 10Eier Ruge W. What is primary and what is secondary for amyloid deposition in Alzheimer's disease[J]? Ann NY Acad Sci, 1994;719:23-27.

共引文献28

同被引文献33

  • 1姚柏春,袁华,黄翔.海马注射Aβ_(1~40)诱导大鼠记忆减退及其脑内细胞周期蛋白A的异常表达[J].郧阳医学院学报,2004,23(4):193-196. 被引量:19
  • 2Hirai K, Aliev G, Nunomura A, et al. Mitochondrial abnormalities in Alzheimer's disease[J]. Neuroscience,2001 ;21:3017-23.
  • 3Aksenov MY, Tucker HM, Nair P, et al. The expression of several mitochondrial and nuclear genes encoding the subunits of electron transport chain enzyme complexes cytochrome C oxidase, and NADH dehydrogenase, in different brain regions in Alzheimer' s disease [J]. Neurochem Res. 1999 ;24:767-74.
  • 4Hashimoto M, Rockenstein E, Crews L, et al. Role of protein aggregation in mitochondrial dysfunction and neurodegeneration in Alzheimer's and Parkinson's diseases[ J]. Neuromoleeular Med ,2003 ;4 ( 1-2 ) :21-36.
  • 5Cardoso SM, Santos S, Swerdlow RH, et al. Functional mitochondria are required for amyloid mediated neurotoxicity [ J]. FASEB J, 2001 ; 15 : 143941.
  • 6Praag H, Schinder AF, Christie BR ,et al, Functional neurogenesis in the adult hippocampus[ J]. Nature ,2002 ;415 : 1030-4.
  • 7Hardy J, Selkoe DJ. T'he amyloid hypothesis of Alzheimer's disease:progress and problems on the road to therapeutics[ J ]. Science, 2002 ;297: 353-6.
  • 8Hirai K,Aliev G,Nunomura A,et al. Mitochondrial abnormalities in Alzheimer's disease[J].Neurosci,2001;21:3017-23.
  • 9Aksenov MY,Tucker HM,Nair P,et al. The expression of several mitochondrial and nuclear genes encoding the subunits of electron transport chain enzyme complexes cytochrome C oxidase,and NADH dehydrogenase,in different brain regions in Alzheimer's disease[J]. Neurochem Res,1999;24:767-74.
  • 10Hashimoto M,Rockenstein E,Crews L,et al. Role of protein aggregation in mitochondrial dysfunction and neurodegeneration in Alzheimer's and Parkinson's diseases[J]. Neuromol Med,2003;4(1-2):21-36.

引证文献3

二级引证文献13

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