Brandeis University, Waltham, MA 02453, USA.
Helen Wills Neuroscience Institute, University of California Berkeley, Berkeley, CA 94720, USA.
Neurosci Biobehav Rev. 2023 Jul;150:105192. doi: 10.1016/j.neubiorev.2023.105192. Epub 2023 Apr 20.
The basal forebrain cholinergic system (BFCS) has long been implicated in age-related cognitive changes and the pathophysiology of Alzheimer's disease (AD). Limitations of cholinergic interventions helped to inspire a shift away from BFCS in AD research. A resurgence in interest in the BFCS following methodological and analytical advances has resulted in a call for the BFCS to be examined in novel frameworks. We outline the basic structure and function of the BFCS, its role in supporting cognitive and affective function, and its vulnerability to aging and AD. We consider the BFCS in the context of the amyloid hypothesis and evolving concepts in AD research: resilience and resistance to pathology, selective neuronal vulnerability, trans-synaptic pathology spread and sleep health. We highlight 1) the potential role of the BFCS in cognitive resilience, 2) recent work refining understanding about the selective vulnerability of BFCS to AD, 3) BFCS connectivity that suggests it is related to tau spreading and neurodegeneration and 4) the gap between BFCS involvement in AD and sleep-wake cycles.
基底前脑胆碱能系统(BFCS)长期以来一直与年龄相关的认知变化和阿尔茨海默病(AD)的病理生理学有关。胆碱能干预的局限性有助于激发 AD 研究中对 BFCS 的转移。随着方法和分析上的进步,人们对 BFCS 的兴趣重新高涨,呼吁在新的框架中检查 BFCS。我们概述了 BFCS 的基本结构和功能、它在支持认知和情感功能方面的作用,以及它对衰老和 AD 的脆弱性。我们考虑了 BFCS 在淀粉样蛋白假说和 AD 研究中不断发展的概念的背景下:对病理的弹性和抵抗力、选择性神经元脆弱性、跨突触病理传播和睡眠健康。我们强调了 1)BFCS 在认知弹性中的潜在作用,2)最近关于 BFCS 对 AD 选择性脆弱性的理解的工作,3)BFCS 连接性表明它与 tau 传播和神经退行性变有关,以及 4)BFCS 参与 AD 和睡眠-觉醒周期之间的差距。