Insulin resistance and Alzheimer's disease

被引:310
作者
de la Monte, Suzanne M. [1 ,2 ,3 ,4 ]
机构
[1] Rhode Isl Hosp, Dept Neurol, Providence, RI USA
[2] Rhode Isl Hosp, Dept Pathol, Providence, RI 02902 USA
[3] Rhode Isl Hosp, Dept Med, Providence, RI 02902 USA
[4] Brown Univ, Warren Alpert Med Sch, Providence, RI 02912 USA
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; Central nervous system; Ceramid; Diabetes mellitus; Insulin resistance; Neurodegeneration; Non-alcoholic steatohepatitis; Obesity; Streptozotocin; GROWTH-FACTOR EXPRESSION; RECEPTOR SIGNAL-TRANSDUCTION; DIABETES-MELLITUS; DEGRADING ENZYME; FACTOR-I; GLUCOSE-METABOLISM; BRAIN; PROTEIN; TAU; PHOSPHORYLATION;
D O I
10.5483/BMBRep.2009.42.8.475
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
Emerging data demonstrate pivotal roles for brain insulin resistance and insulin deficiency as mediators of cognitive impairment and neurodegeneration, particularly Alzheimer's disease (AD). Insulin and insulin-like growth factors (IGFs) regulate neuronal survival, energy metabolism, and plasticity, which are required for learning and memory. Hence, endogenous brain-specific impairments in insulin and IGF signaling account for the majority of AD-associated abnormalities. However, a second major mechanism of cognitive impairment has been linked to obesity and Type 2 diabetes (T2DM). Human and experimental animal studies revealed that neurodegeneration associated with peripheral insulin resistance is likely effectuated via a liver-brain axis whereby toxic lipids, including ceramides, cross the blood brain barrier and cause brain insulin resistance, oxidative stress, neuro-inflammation, and cell death. In essence, there are dual mechanisms of brain insulin resistance leading to AD-type neurodegeneration: one mediated by endogenous, CNS factors; and the other, peripheral insulin resistance with excess cytotoxic ceramide production. [BMB reports 2009; 42(8): 475-481]
引用
收藏
页码:475 / 481
页数:7
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