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慢性低氧低糖培养影响新生大鼠海马神经元α-分泌酶的实验研究 被引量:1

An experimental study of the effect on α-secretase of rat hippocampal neurons after chronic hypoxic and hypoglycemic culture
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摘要 目的探讨慢性低氧低糖培养对新生大鼠海马神经元α-分泌酶活性及表达的影响。方法取新生24h的Wistar大鼠海马原代培养神经元并予以鉴定,培养第七天予以12h、24h、36h低氧低糖培养干预,MTT法检测海马神经元的活力,荧光法检测α、β-分泌酶活性,Western blot检测α-分泌酶蛋白表达水平。结果低氧低糖培养12小时组海马神经元α-分泌酶活性升高(P<0.01),低氧低糖培养24h、36h组α-分泌酶(TACE)活性无明显变化(P>0.05),低氧低糖培养12h、24h、36h组海马神经元β-分泌酶(BACE1)活性升高(P<0.05);低氧低糖培养12h、24h、36h组海马神经元α-分泌酶蛋白表达水平降低(P<0.05)。结论慢性低氧低糖培养降低新生大鼠海马神经元α-分泌酶的表达。 Objective To investigate tbe effect of chronic hypoxic and hypoglycemic culture on α-secretase activities and expression of rat hippocampal neurons. Methods Primary cultures of Wistar rat hippoeampal neurons were prepared for the following procedures. At 7th day after cells plating,hippocampal neurons were treated with hy- poxic and hypoglycemic euhure for 12h,24h,and 36h respectively. Cells vitality were assayed by MTT, fluorescence detection and Western blot were applied respectively to assay tx-seeretase expression and activity. Results The ac- tivity of tx-secretase was increased at 12h time point( P 〈 0.01 ) and no significantly alterations at other time points( P 〉 0.05 ) , β-secretase activity was increased at all time points ( P 〈 0.05 ) ; α-secretase expression was desereased at all time points after chronic hypoxic and hypoglycemic culture(P 〈 0.05). Conclusion α-secretase expression and activity of rat hippocampal neurons changed after chronic hypoxic and hypoglycemie culture.
出处 《脑与神经疾病杂志》 2009年第2期141-144,共4页 Journal of Brain and Nervous Diseases
关键词 阿尔茨海默病 慢性低氧低糖培养 海马神经元 Α-分泌酶 Β-分泌酶 Alzheimer disease chronic hypoxic and hypoglycemic culture hippocampal neuron α-secretase β-secretase
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参考文献14

  • 1Mattson MP.Pathways towards and away from Alzheimer's disease.Nature,2004,430:631-639. 被引量:1
  • 2Kalaria RN.The role of cerebral ischemia in Alzheimer's disease.Neurobiol.Aging,2000,21:321-333. 被引量:1
  • 3Webster NJ,Green KN,Peers C,et al.Altered processing of amyloid precursor protein in the human neuroblastoma SH-SY5Y by chronic hypoxia.Neurochem,2002,83:1262-1271. 被引量:1
  • 4Vassar R,Martin C.Aβ-generating enzymes:Recent advances in β-and γ-secretase research.Neuron,2000,27:419-422. 被引量:1
  • 5Snowdon DA,Greiner LH,Mortimer JA,et al.Brain infarction and theclinical expression of Alzheimer's disease:the Nun study.JAMA,1997,277:813-817. 被引量:1
  • 6Pohjasvaara T,Erkinjuntti T,Ylikoski R,et al.Clinical determinants of poststrokedementia.Stroke,1998,29:75-81. 被引量:1
  • 7Asahara T,Masuda H,Takahashi T,et al.Bonemarrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization.Circ Res,1999,85:221-228. 被引量:1
  • 8Popa-Wagner A,Schroder E,Walker L C,et al.β-amyloid precursor protein and β-amyloid peptide immunoreactivity in the brain after middle cerebral artery occlusion.Stroke,1998,29:2196-2202. 被引量:1
  • 9Hall ED,Oostveen JA,Dunn E,et al.Increased amyloid protein precursor and apolipprotein E immunoreactivity in the selectively vulnerable hippocampus following transient forebrain ischemia in gerbils.Exp Neuro,1995,135:17-27. 被引量:1
  • 10Groen TV,Puurunen K,Maki HM,et al.Transformation of Diffuse[beta]-Amyloid Precursor Protein and[beta]-Amyloid Deposits to Plaques in the Thalamus After Transient Occlusion of the Middle Cerebral Artery in Rats.Stroke,2005,36:1551-1556. 被引量:1

二级参考文献19

  • 1Jack C,De la Torre JC.Is Alzheimer's disease a neurodegenerative or a vascular disorder? Data,dogma,and dialectics[J].Lancet Neurology,2004,3:184-190 被引量:1
  • 2De Carli C.The role of cerebrovascular disease in dementia[J].Neurology,2003,9:123-136 被引量:1
  • 3Jellinger KA,Mitter-Ferst E.The impact of cerebrovascular lesions in Alzheimer's disease.A comaprative autopsy study[J].J Neurol,2003,250:1050-1055 被引量:1
  • 4De-la Torre JC,Fortin T,Park GAS,et al.Brain blood flow restoration 'rescues'chronically damaged rat CA1 neurons[J].Brain Res,1993,623:6-15 被引量:1
  • 5Wakita H,Tominoto H,Kimurua J.Glia activation and white matter change in the rat brain induced by chronic cerebral by hypoperfusion:an immunohischemical study[J].Acta Neuropathol Berl,1993,87:484-492 被引量:1
  • 6Tyler SJ,Dawbarn D,Wilcock GK,et al.Alpha-and beta-secretase:profound changes in Alzheimer's disease[J].Biochem Biophys Res Commun,2002,299:373-376 被引量:1
  • 7Selkoe DJ.Cell biology of the amyloid beta-protein precursor and the mechanism of Alzheimer's disease[J].Annu Rev Cell Biol,1994,10:373-403 被引量:1
  • 8Bodendorf U,Danner S,Fischer F,et al.Expression of human beta-secretase in the mouse brain increases the steady-state level of beta-amyloid[J].J Neurochem,2002,80:799-806 被引量:1
  • 9Vassar R.The beta-secretase,BACE:a prime drug target for Alzheimer's disease[J].J Mol Neurosci,2001,17:157-170 被引量:1
  • 10Cai H,Wang Y,McCarthy D,et al.BACE1 is the major β-secretase for generation of A β peptides by neurons[J].Nat Neurosci,2001,4:233-234 被引量:1

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