Alzheimer's disease & metals: therapeutic opportunities

作者：Kenche Vijaya B; Barnham Kevin J^*

来源：British Journal of Pharmacology, 2011, 163(2): 211-219.

DOI：10.1111/j.1476-5381.2011.01221.x

• copper
• zinc
• amyloid
• synaptic toxicity
• homeostasis
• oxidative stress
• chelator
• bioinorganic chemistry
• drug

Alzheimer's disease (AD) is the most common age related neurodegenerative disease. Currently, there are no disease modifying drugs, existing therapies only offer short-term symptomatic relief. Two of the pathognomonic indicators of AD are the presence of extracellular protein aggregates consisting primarily of the A beta peptide and oxidative stress. Both of these phenomena can potentially be explained by the interactions of A beta with metal ions. In addition, metal ions play a pivotal role in synaptic function and their homeostasis is tightly regulated. A breakdown in this metal homeostasis and the generation of toxic A beta oligomers are likely to be responsible for the synaptic dysfunction associated with AD. Therefore, approaches that are designed to prevent A beta metal interactions, inhibiting the formation of toxic A beta species as well as restoring metal homeostasis may have potential as disease modifying strategies for treating AD. This review summarizes the physiological and pathological interactions that metal ions play in synaptic function with particular emphasis placed on interactions with A beta. A variety of therapeutic strategies designed to address these pathological processes are also described. The most advanced of these strategies is the so-called 'metal protein attenuating compound' approach, with the lead molecule PBT2 having successfully completed early phase clinical trials. The success of these various strategies suggests that manipulating metal ion interactions offers multiple opportunities to develop disease modifying therapies for AD.

• 出版日期2011-5