Institute for Memory Impairments and Neurological Disorders, University of California, Irvine, CA 92697, USA.
Institute for Memory Impairments and Neurological Disorders, University of California, Irvine, CA 92697, USA; Department of Neurobiology and Behavior, University of California, Irvine, CA 92697, USA.
Trends Neurosci. 2017 Jun;40(6):347-357. doi: 10.1016/j.tins.2017.04.002. Epub 2017 May 8.
Alzheimer's disease (AD) is characterized by memory loss, cognitive decline, and devastating neurodegeneration, not only as a result of the extracellular accumulation of beta-amyloid peptide (Aβ) and intracellular accumulation of tau, but also as a consequence of the dysfunction and loss of synapses. Although significant advances have been made in our understanding of the relationship of the pathological role of Aβ and tau in synapse dysfunction, several questions remain as to how Aβ and tau interdependently cause impairments in synaptic function in AD. Overall, more insight into these questions should enable researchers in this field to develop novel therapeutic targets to mitigate or delay the cognitive deficits associated with this devastating disease.
阿尔茨海默病(AD)的特征是记忆丧失、认知能力下降和毁灭性的神经退行性变,这不仅是由于细胞外β-淀粉样肽(Aβ)的积累和细胞内 tau 的积累,还由于突触的功能障碍和丧失。尽管我们对 Aβ和 tau 的病理作用与突触功能障碍之间的关系有了重大的了解,但关于 Aβ和 tau 如何相互作用导致 AD 中突触功能受损,仍有几个问题尚未解决。总的来说,对这些问题的更深入了解应该使该领域的研究人员能够开发新的治疗靶点,以减轻或延缓与这种毁灭性疾病相关的认知缺陷。