Kawahara Masahiro
Department of Analytical Chemistry, School of Pharmaceutical Sciences, Kyushu University of Health and Welfare, Nobeoka-city, Miyazaki, 882-8508, Japan.
J Alzheimers Dis. 2005 Nov;8(2):171-82; discussion 209-15. doi: 10.3233/jad-2005-8210.
Aluminum is environmentally abundant, but not an essential element. Aluminum has been associated with several neurodegenerative diseases, such as dialysis encephalopathy, amyotrophic lateral sclerosis and Parkinsonism dementia in the Kii peninsula and Guam, and in particular, Alzheimer's disease. Although this association remains controversial, there is increasing evidence which suggests the implication of metal homeostasis in the pathogenesis of Alzheimer's disease. Aluminum, zinc, copper, and iron cause the conformational changes of Alzheimer's amyloid-beta protein. Al causes the accumulation of tau protein and amyloid-beta protein in experimental animals. Aluminum induces neuronal apoptosis in vivo as well as in vitro. Furthermore, a relationship between aluminum and the iron-homeostasis or calcium-homeostasis has been suggested. Based on these findings, the characteristics of aluminum neurotoxicity are reviewed, and the potential link between aluminum and neurodegenerative diseases is reconsidered.
铝在环境中含量丰富,但并非必需元素。铝与多种神经退行性疾病有关,如透析性脑病、肌萎缩侧索硬化症以及日本纪伊半岛和关岛的帕金森痴呆症,尤其是阿尔茨海默病。尽管这种关联仍存在争议,但越来越多的证据表明金属稳态在阿尔茨海默病发病机制中起作用。铝、锌、铜和铁会导致阿尔茨海默病β淀粉样蛋白的构象变化。铝会导致实验动物体内tau蛋白和β淀粉样蛋白的积累。铝在体内和体外均可诱导神经元凋亡。此外,铝与铁稳态或钙稳态之间的关系也已被提出。基于这些发现,对铝神经毒性的特征进行了综述,并重新审视了铝与神经退行性疾病之间的潜在联系。