脂筏
神经科学
神经退行性变
突触可塑性
长时程增强
胆固醇
星形胶质细胞
细胞内
阿尔茨海默病
疾病
生物
化学
细胞生物学
内分泌学
内科学
医学
生物化学
受体
中枢神经系统
出处
期刊:Cornell University - arXiv
日期:2023-01-01
标识
DOI:10.48550/arxiv.2310.20232
摘要
I present a theory of Alzheimer's Disease (AD) that explains its symptoms, pathology, and risk factors. To do this, I introduce a new theory of brain plasticity that elucidates the physiological roles of AD-related agents. New events generate synaptic and branching candidates competing for long-term enhancement. Competition resolution crucially depends on the formation of membrane lipid rafts, which requires astrocyte-produced cholesterol. Sporadic AD is caused by impaired formation of plasma membrane lipid rafts, which prevents the conversion of short- to long-term memory, and yields excessive tau phosphorylation, intracellular cholesterol accumulation, synaptic dysfunction, and neurodegeneration. Amyloid beta (Abeta) production is promoted by cholesterol during the switch to competition resolution, and cholesterol accumulation stimulates chronic Abeta production, secretion, and aggregation. The theory addresses all of the major established facts known about the disease, and is supported by strong evidence.
科研通智能强力驱动
Strongly Powered by AbleSci AI