期刊文献+

Mitochondrial dysfunction and cellularmetabolic deficiency in Alzheimer's disease 被引量:8

Mitochondrial dysfunction and cellularmetabolic deficiency in Alzheimer's disease
原文传递
导出
摘要 Alzheimer's disease (AD) is an age-related neurodegenerative disorder. The pathology of AD includes amyloid-β (Aβ) deposits in neuritic plaques and neurofibrillary tangles composed of hyperphosphorylated tau, as well as neuronal loss in specific brain regions. Increasing epidemiological and functional neuroimaging evidence indicates that global and regional disruptions in brain metabolism are involved in the pathogenesis of this disease. Aβ precursor protein is cleaved to produce both extracellular and intracellular Aβ, accumulation of which might interfere with the homeostasis of cellular metabolism. Mitochondria are highly dynamic organelles that not only supply the main energy to the cell but also regulate apoptosis. Mitochondrial dysfunction might contribute to Aβ neurotoxicity. In this review, we summarize the pathways ofAβ generation and its potential neurotoxic effects on cellular metabolism and mitochondrial dysfunction. Alzheimer's disease (AD) is an age-related neurodegenerative disorder. The pathology of AD includes amyloid-β (Aβ) deposits in neuritic plaques and neurofibrillary tangles composed of hyperphosphorylated tau, as well as neuronal loss in specific brain regions. Increasing epidemiological and functional neuroimaging evidence indicates that global and regional disruptions in brain metabolism are involved in the pathogenesis of this disease. Aβ precursor protein is cleaved to produce both extracellular and intracellular Aβ, accumulation of which might interfere with the homeostasis of cellular metabolism. Mitochondria are highly dynamic organelles that not only supply the main energy to the cell but also regulate apoptosis. Mitochondrial dysfunction might contribute to Aβ neurotoxicity. In this review, we summarize the pathways ofAβ generation and its potential neurotoxic effects on cellular metabolism and mitochondrial dysfunction.
出处 《Neuroscience Bulletin》 SCIE CAS CSCD 2012年第5期631-640,共10页 神经科学通报(英文版)
基金 supported by the National Natural Science Foundation of China(31071512) the Subsidy for Outstanding People of Beijing Municipality, China (2012D005022000006) the Project for Academic Human Resources Development in Institutions of Higher Learning Under the Jurisdiction of Beijing Municipality, China [PHR(IHLB), PHR20090514]
关键词 Alzheimer’s disease amyloid-β metabolic deficiency mitochondrial dysfunction Alzheimer’s disease; amyloid-β; metabolic deficiency; mitochondrial dysfunction
  • 相关文献

参考文献82

  • 1Huang HC, Jiang ZF. Amyloid-beta protein precursor family mem- bers: a review from homology to biological function. J Alzheimers Dis 2011, 26: 607-626.
  • 2Huang HC, Jiang ZF. Accumulated amyloid-beta peptide and hy- perphosphorylated tau protein: relationship and links in Alzheimer's disease. J Alzheimers Dis 2009, 16: 15-27.
  • 3Kapogiannis D, Mattson MP. Disrupted energy metabolism and neuronal circuit dysfunction in cognitive impairment and Alzheim- er's disease. Lancet Neurol 2011, 10:187-198.
  • 4Sultana R, Mecocci P, Mangialasche F, Cecchetti R, Baglioni M, Butterfield DA. Increased protein and lipid oxidative damage in mi- tochondria isolated from lymphocytes from patients with Alzheim- er's disease: insights into the role of oxidative stress in Alzheimer's disease and initial investigations into a potential biomarker for this dementing disorder. J Alzheimers Dis 2011, 24: 77-84.
  • 5Ishii K, Sasaki M, Kitagaki H, Yamaji S, Sakamoto S, Matsuda K, et al. Reduction of cerebellar glucose metabolism in advanced A1- zheimer's disease. J Nucl Med 1997, 38: 925-928.
  • 6Kennedy AM, Frackowiak RS, Newman SK, Bloomfield PM, Seaward J, Roques P, et al. Deficits in cerebral glucose metabolism demon- strated by positron emission tomography in individuals at risk of familial Alzheimer's disease. Neurosci Lett 1995, 186:17-20.
  • 7Furst A J, Lal RA. Amyloid-beta and glucose metabolism in A1- zheimer's disease. J Alzheimers Dis 2011, 26 (Suppl 3): 105-116.
  • 8Hoyer S. Glucose metabolism and insulin receptor signal transduc- tion in Alzheimer disease. Eur J Pharmacol 2004, 490:115-125.
  • 9Young-Collier KJ, McArdle M, Bennett JP. The dying of the light: mitochondrial failure in Alzheimer's disease. J Alzheimers Dis 2012, 28: 771-781.
  • 10Liang WS, Reiman EM, Valla J, Dunckley T, Beach TG, Grover A, et al. Alzheimer's disease is associated with reduced expression of energy metabolism genes in posterior cingulate neurons. Proe Natl Acad Sci U S A 2008, 105: 4441-4446.

同被引文献21

引证文献8

二级引证文献29

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