Department of Gene Technology, Tallinn University of Technology, Akadeemia tee 15, Tallinn 12618, Estonia.
Neurochem Int. 2013 Mar;62(4):367-78. doi: 10.1016/j.neuint.2013.01.023. Epub 2013 Feb 6.
Progressive deposition of amyloid beta (Aβ) peptides into amyloid plaques is the pathological hallmark of Alzheimer's disease (AD). The amyloid cascade hypothesis pins this deposition as the primary cause of the disease, but the mechanisms that causes this deposition remain elusive. An increasing amount of evidence shows that biometals Zn(II) and Cu(II) can interact with Aβ, thus influencing the fibrillization and toxicity. This review focuses on the role of Zn(II) and Cu(II) in AD, and revisits the amyloid cascade hypothesis demonstrating the possible roles of Zn(II) and Cu(II) in the disease pathogenesis.
淀粉样β(Aβ)肽的进行性沉积形成淀粉样斑块是阿尔茨海默病(AD)的病理标志。淀粉样蛋白级联假说将这种沉积视为疾病的主要原因,但导致这种沉积的机制仍不清楚。越来越多的证据表明,生物金属 Zn(II) 和 Cu(II) 可以与 Aβ相互作用,从而影响纤维形成和毒性。本综述重点讨论了 Zn(II) 和 Cu(II) 在 AD 中的作用,并重新审视了淀粉样蛋白级联假说,展示了 Zn(II) 和 Cu(II) 在疾病发病机制中的可能作用。