在大脑发育过程中,拮抗剂与n -甲基- d -天冬氨酸受体的慢性结合导致神经退行性变,并在衰老过程中导致学习和记忆障碍

F. Tschudi-Monnet, R. Fitzgerald
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引用次数: 3

摘要

该AOP将大脑发育过程中的慢性NMDA受体抑制与海马和皮层的神经变性、淀粉样斑块沉积和tau过度磷酸化以及学习和记忆障碍联系起来,这些被认为是阿尔茨海默病的标志。它利用了AOP 13中的一些KEs和KERs,并将神经炎症作为KE引入,它与几种神经退行性疾病有关。这个AOP是基于Landrigan和他的同事(2005)提出的神经退行性疾病在晚年早期起源的假设。在本AOP中用于经验支持的化学引发剂是铅(Pb)。在成人中,终生累积铅暴露也与认知能力下降有关,这表明在发育过程中或职业暴露期间长期暴露于铅会增加患神经退行性疾病的风险。暴露和迟发效应之间的长潜伏期使其具有非常广泛的生命阶段适用性。知识的差距主要是由于有限的定量评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adverse Outcome Pathway on chronic binding of antagonist to N-methyl-D-aspartate receptors during brain development leading to neurodegeneration with impairment in learning and memory in aging
This AOP links chronic NMDA receptors inhibition during brain development to neurodegeneration in hippocampus and cortex with amyloid plaque deposition and tau hyperphosphorylation, and impairment of learning and memory, which are considered as hallmark of Alzheimer's disease. It makes use of some KEs and KERs from AOP 13 and introduces Neuroinflammation as KE, which is involved in several neurodegenerative diseases. This AOP is based on the hypothesis of Landrigan and coworkers (2005) proposing an early origin of neurodegenerative diseases in later life. The chemical initiator used in this AOP for the empirical support is lead (Pb). In adults, cumulative lifetime Pb exposure is also associated with decline in cognition, suggesting that long-term exposure during development or occupational exposure increases the risk to develop neurodegenerative disease. The long latency period between exposure and late-onset of effects gives a very broad life-stage applicability. The gap of knowledge is mainly due to limited quantitative evaluations.
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