Department of Biomedical and Biotechnological Sciences, Section of Pharmacology, University of Catania, Catania, Italy.
CNS Neurosci Ther. 2019 Jan;25(1):5-13. doi: 10.1111/cns.13050. Epub 2018 Aug 12.
Alzheimer's disease (AD) is characterized by extensive neurodegeneration and inflammation in selective brain areas, linked to severely disabling cognitive deficits. Before full manifestation, different stages appear with progressively increased brain pathology and cognitive impairment. This significantly extends the time lag between initial molecular triggers and appearance of detectable symptoms. Notably, a number of studies in the last decade have revealed that in the early stage of mild cognitive impairment, events that appear in contrast with neuronal distress may occur. These have been reproduced in vitro and in animal models and include increase in synaptic elements, increase in synaptic and metabolic activity, enhancement of neurotrophic milieu and changes in glial cell reactivity and inflammation. They have been interpreted as compensatory responses that could either delay disease progression or, in the long run, result detrimental. For this reason, these mechanisms define a new and previously undervalued window of opportunity for intervention. Their importance resides especially in their early appearance. Directing efforts to better characterize this stage, in order to identify new pharmacological targets, is an exciting new avenue to future advances in AD research.
阿尔茨海默病(AD)的特征是选择性大脑区域广泛的神经退行性变和炎症,与严重的认知障碍相关。在完全表现之前,不同的阶段出现,伴随着逐渐增加的脑病理学和认知障碍。这大大延长了最初的分子触发和可检测症状出现之间的时间间隔。值得注意的是,过去十年的许多研究表明,在轻度认知障碍的早期阶段,可能会出现与神经元压力相反的事件。这些在体外和动物模型中得到了重现,包括突触成分的增加、突触和代谢活性的增加、神经营养环境的增强以及神经胶质细胞反应性和炎症的变化。它们被解释为代偿性反应,可能会延迟疾病进展,或者从长远来看,导致不利后果。因此,这些机制定义了一个新的、以前被低估的干预机会窗口。它们的重要性尤其在于它们的早期出现。努力更好地描述这一阶段,以确定新的药理学靶点,是 AD 研究未来进展的一个令人兴奋的新途径。