Relationship between Brain Metabolic Disorders and Cognitive Impairment: LDL Receptor Defect

被引:20
|
作者
Hong, Dong-Yong [1 ,2 ]
Lee, Dong-Hun [1 ,2 ]
Lee, Ji-Young [1 ]
Lee, Eun-Chae [1 ,2 ]
Park, Sang-Won [1 ,2 ]
Lee, Man-Ryul [2 ]
Oh, Jae-Sang [1 ,2 ]
机构
[1] Soonchunhyang Univ, Cheonan Hosp, Dept Neurosurg, Coll Med, Cheonan 31151, South Korea
[2] Soon Chun Hyang Univ, Soonchunhyang Inst Med Bio Sci SIMS, Cheonan 31151, South Korea
基金
新加坡国家研究基金会;
关键词
cholesterol metabolism; LDLr; insulin receptor; SREBP; blood-brain-barrier (BBB) breakdown; neuroinflammation; ER stress; mitochondria; apoptosis; lectin-like oxidized LDL receptor-1 (LOX-1); LOW-DENSITY-LIPOPROTEIN; CENTRAL-NERVOUS-SYSTEM; ENDOPLASMIC-RETICULUM STRESS; UNFOLDED PROTEIN RESPONSE; MODULAR ADAPTER PROTEIN; HIGH CHOLESTEROL DIET; ALZHEIMERS-DISEASE; APOLIPOPROTEIN-E; FAMILIAL HYPERCHOLESTEROLEMIA; OXIDATIVE STRESS;
D O I
10.3390/ijms23158384
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The low-density-lipoprotein receptor (LDLr) removes low-density lipoprotein (LDL), an endovascular transporter that carries cholesterol from the bloodstream to peripheral tissues. The maintenance of cholesterol content in the brain, which is important to protect brain function, is affected by LDLr. LDLr co-localizes with the insulin receptor and complements the internalization of LDL. In LDLr deficiency, LDL blood levels and insulin resistance increase, leading to abnormal cholesterol control and cognitive deficits in atherosclerosis. Defects in brain cholesterol metabolism lead to neuroinflammation and blood-brain-barrier (BBB) degradation. Moreover, interactions between endoplasmic reticulum stress (ER stress) and mitochondria are induced by ox-LDL accumulation, apolipoprotein E (ApoE) regulates the levels of amyloid beta (A beta) in the brain, and hypoxia is induced by apoptosis induced by the LDLr defect. This review summarizes the association between neurodegenerative brain disease and typical cognitive deficits.
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页数:15
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