IRCCS S. Lucia Foundation, Via del Fosso di Fiorano 65, 00143 Rome, Italy.
Prog Neurobiol. 2012 Oct;99(1):42-60. doi: 10.1016/j.pneurobio.2012.07.001. Epub 2012 Jul 10.
The human brain contains about 100 billion neurons forming an intricate network of innumerable connections, which continuously adapt and rewire themselves following inputs from external and internal environments as well as the physiological synaptic, dendritic and axonal sculpture during brain maturation and throughout the life span. Growing evidence supports the idea that Alzheimer's disease (AD) targets selected and functionally connected neuronal networks and, specifically, their synaptic terminals, affecting brain connectivity well before producing neuronal loss and compartmental atrophy. The understanding of the molecular mechanisms underlying the dismantling of neuronal circuits and the implementation of 'clinically oriented' methods to map-out the dynamic interactions amongst neuronal assemblies will enhance early/pre-symptomatic diagnosis and monitoring of disease progression. More important, this will open the avenues to innovative treatments, bridging the gap between molecular mechanisms and the variety of symptoms forming disease phenotype. In the present review a set of evidence supports the idea that altered brain connectivity, exhausted neural plasticity and aberrant neuronal activity are facets of the same coin linked to age-related neurodegenerative dementia of Alzheimer type. Investigating their respective roles in AD pathophysiology will help in translating findings from basic research to clinical applications.
人类大脑包含大约 1000 亿个神经元,形成一个错综复杂的网络,其中无数的连接不断地适应和重新布线,以响应来自外部和内部环境的输入,以及大脑成熟和整个生命周期中生理突触、树突和轴突的塑造。越来越多的证据支持这样一种观点,即阿尔茨海默病(AD)靶向选定的和功能连接的神经元网络,特别是它们的突触末梢,并在产生神经元丧失和隔室萎缩之前影响大脑连接。了解导致神经元回路解体的分子机制,并实施“以临床为导向”的方法来描绘神经元集合之间的动态相互作用,将有助于早期/无症状诊断和监测疾病进展。更重要的是,这将为创新治疗开辟道路,弥合分子机制与形成疾病表型的各种症状之间的差距。在本综述中,有一组证据支持这样一种观点,即改变的大脑连接、耗尽的神经可塑性和异常的神经元活动是与年龄相关的阿尔茨海默型神经退行性痴呆相关的同一枚硬币的不同方面。研究它们在 AD 病理生理学中的各自作用将有助于将基础研究的发现转化为临床应用。