Watt Nicole T, Whitehouse Isobel J, Hooper Nigel M
Institute of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Clarendon Way, Leeds LS2 9JT, UK.
Int J Alzheimers Dis. 2010 Dec 20;2011:971021. doi: 10.4061/2011/971021.
Zinc, the most abundant trace metal in the brain, has numerous functions, both in health and in disease. Zinc is released into the synaptic cleft of glutamatergic neurons alongside glutamate from where it interacts and modulates NMDA and AMPA receptors. In addition, zinc has multifactorial functions in Alzheimer's disease (AD). Zinc is critical in the enzymatic nonamyloidogenic processing of the amyloid precursor protein (APP) and in the enzymatic degradation of the amyloid-β (Aβ) peptide. Zinc binds to Aβ promoting its aggregation into neurotoxic species, and disruption of zinc homeostasis in the brain results in synaptic and memory deficits. Thus, zinc dyshomeostasis may have a critical role to play in the pathogenesis of AD, and the chelation of zinc is a potential therapeutic approach.
锌是大脑中含量最丰富的痕量金属,在健康和疾病状态下均具有多种功能。锌与谷氨酸一起释放到谷氨酸能神经元的突触间隙中,并在那里与N-甲基-D-天冬氨酸(NMDA)和α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体相互作用并对其进行调节。此外,锌在阿尔茨海默病(AD)中具有多方面的作用。锌在淀粉样前体蛋白(APP)的非淀粉样生成酶促加工过程以及淀粉样β(Aβ)肽的酶促降解过程中至关重要。锌与Aβ结合,促进其聚集成神经毒性物质,而大脑中锌稳态的破坏会导致突触和记忆缺陷。因此,锌稳态失衡可能在AD的发病机制中起关键作用,而锌螯合是一种潜在的治疗方法。