期刊文献+

Environmental factors in the development and progression of late-onset Alzheimer's disease 被引量:6

Environmental factors in the development and progression of late-onset Alzheimer's disease
原文传递
导出
摘要 Late-onset Alzheimer's disease (LOAD) is an age-related neurodegenerative disorder characterized by gradual loss of synapses and neurons, but its pathogenesis remains to be clarified. Neurons live in an environment constituted by neurons themselves and glial cells. In this review, we propose that the neuronal degeneration in the AD brain is partially caused by diverse environmental factors. We first discuss various environmental stresses and the corresponding responses at different levels. Then we propose some mechanisms underlying the specific pathological changes, in particular, hypothalamic-pituitary adrenal axis dysfunction at the systemic level; cerebrovascular dysfunction, metal toxicity, glial activation, and Aβ toxicity at the intercellular level; and kinase-phosphatase imbalance and epigenetic modification at the intracellular level. Finally, we discuss the possibility of developing new strategies for the prevention and treatment of LOAD from the perspective of environmental stress. We conclude that environmental factors play a significant role in the development of LOAD through multiple pathological mechanisms. Late-onset Alzheimer's disease (LOAD) is an age-related neurodegenerative disorder characterized by gradual loss of synapses and neurons, but its pathogenesis remains to be clarified. Neurons live in an environment constituted by neurons themselves and glial cells. In this review, we propose that the neuronal degeneration in the AD brain is partially caused by diverse environmental factors. We first discuss various environmental stresses and the corresponding responses at different levels. Then we propose some mechanisms underlying the specific pathological changes, in particular, hypothalamic-pituitary adrenal axis dysfunction at the systemic level; cerebrovascular dysfunction, metal toxicity, glial activation, and Aβ toxicity at the intercellular level; and kinase-phosphatase imbalance and epigenetic modification at the intracellular level. Finally, we discuss the possibility of developing new strategies for the prevention and treatment of LOAD from the perspective of environmental stress. We conclude that environmental factors play a significant role in the development of LOAD through multiple pathological mechanisms.
出处 《Neuroscience Bulletin》 SCIE CAS CSCD 2014年第2期253-270,共18页 神经科学通报(英文版)
基金 supported by National Basic Research Development Program(973 Program)of China(2011CBA00400) the National Natural Science Foundation of China(91332201) the Natural Science Foundation of Shanghai Municipality,China(13JC1401500) the Fund for Medical Emerging Cutting-edge Technology of Shanghai Municipality,China(SHDC12012114)
关键词 Alzheimer's disease environmental factors corticotrophin-releasing factor CEREBROVASCULAR metatoxicity GLIA astrocyte microglia AI3 kinase PHOSPHATASE tau HYPERPHOSPHORYLATION epigenetic modificationDNA methylation histone acetylation Alzheimer's disease environmental factors corticotrophin-releasing factor cerebrovascular metatoxicity glia astrocyte microglia AI3 kinase phosphatase tau hyperphosphorylation epigenetic modificationDNA methylation histone acetylation
  • 相关文献

参考文献223

  • 1Kagias K, Nehammer C, Pocock R. Neuronal responses to physiological stress. Front Genet 2012, 3: 222.
  • 2Stanton ML, environments Roy BA, Thiede DA. Evolution in stressfu and response I. Phenotypic variability, phenotypic selection to selection in five distinct environmenta stresses. Evolution 2000, 54: 93-111.
  • 3Anderegg WR, Berry JA, Field CB. Linking definitions, mechanisms, and modeling of drought-induced tree death. Trends Plant Sci 2012, 17: 693-700.
  • 4Han HW, Ohn JH, Moon J, Kim JH. Yin and Yang of disease genes and death genes between reciprocally scale-free biological networks. Nucleic Acids Res 2013, 41: 9209-9217.
  • 5Fields RD, Araque A, Johansen-Berg H, Lim SS, Lynch G, Nave KA, et al. Glial biology in learning and cognition. Neuroscientist 2013. doi: 10.1177/1073858413504465.
  • 6Pirttimaki TM, Parri HR. Astrocyte plasticity: implications for synaptic and neuronal activity. Neuroscientist 2013, 19: 604-615.
  • 7Kagias K, Nehammer C, Pocock R. Neuronal responses to physiological stress. Front Genet 2012, 3:222.
  • 8Caldji C, Hellstrom IC, Zhang TY, Diorio J, Meaney MJ. Environmental regulation of the neural epigenome. FEBS Lett 2011, 585: 2049-2058.
  • 9Migliore L, Coppede F. Genetics, environmental factors and the emerging role of epigenetics in neurodegenerative diseases. Murat Res 2009, 667: 82-97.
  • 10Debacq-Chainiaux F, Leduc C, Verbeke A, Toussaint O. UV, stress and aging. Dermatoendocrinol 2012, 4: 236-240.

同被引文献98

  • 1陈静,温红博.优秀乒乓球运动员压力来源与应对的质性研究[J].广东技术师范学院学报,2007,28(7):49-55. 被引量:9
  • 2K.库代贝根诺夫,陈遵.高山矿床露天开采境界的确定[J].国外金属矿山,1990(5):39-41. 被引量:1
  • 3Henry W Querfurth , Frank M LaFerla. Alzheimer^Disease[J]. N Engl J Med,2010,362(4):329-344.
  • 4Jean Francois Dartigues . Alzheimer’s disease: a globalchallenge for the 21st century[J]. Lancet Neurol, 2009,8(12):1082-1083.
  • 5David A Bennett,Yu Lei,Yang Jing-yun, et al. Epigenomicsof Alzheimer’s disease[J]. Transl Res, 2015,165 (1):200-220.
  • 6Ignacio F Mata,James Leverenz,Daniel Weintraub,et al.APOE,MAPT,and SNCA genes and cognitive performancein Parkinson disease[J]. JAMA Neurol,2014,71 (11): 1405-1412.
  • 7Irwin David J,Cohen Todd J,Grossman Murray,et al.Acetylated tau,a novel pathological signature in Alzheimer’sdisease and other tauopathies[J]. Brain,2012,135 (Pt 3 ):807-818.
  • 8S Sakura Minami,Min Sang-Won, Grietj e Krabbe, et al.Progranulin protects against amyloid p deposition and toxicityin Alzheimer’s disease mouse models [J]. Nat Med, 2014,20(10):1157-1164.
  • 9Tara L Spires-Jones, Bradley T Hyman. The intersectionof amyloid beta and tau at synapses in Alzheimer’s diseasefJ].Neuron,2014,82 (4): 756-771.
  • 10Min-Kyoo Shin,Hong-Gi Kim,Seung-Hyun Baek,e/ al.Neuropep-1 ameliorates learning and memory deficits in anAlzheimer’s disease mouse model,increases brain-derivedneurotrophic factor expression in the brain, and causesreduction of amyloid beta plaques[J]. Neurobiol Aging,2014,35(5):990-1001.

引证文献6

二级引证文献16

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