Insulin-resistant brain state: The culprit in sporadic Alzheimer's disease?

被引:167
作者
Correia, Sonia C. [2 ,3 ]
Santos, Renato X. [2 ,3 ]
Perry, George [4 ,5 ,6 ]
Zhu, Xiongwei [4 ]
Moreira, Paula I. [1 ,2 ]
Smith, Mark A. [4 ]
机构
[1] Univ Coimbra, Fac Med, Ctr Neurosci & Cell Biol, Inst Physiol, P-3000354 Coimbra, Portugal
[2] Univ Coimbra, Ctr Neurosci & Cell Biol Coimbra, P-3030 Coimbra, Portugal
[3] Univ Coimbra, Fac Sci & Technol, Dept Life Sci, P-3004517 Coimbra, Portugal
[4] Case Western Reserve Univ, Dept Pathol, Cleveland, OH 44106 USA
[5] Univ Texas San Antonio, UTSA Neurosci Inst, San Antonio, TX 78249 USA
[6] Univ Texas San Antonio, Dept Biol, San Antonio, TX 78249 USA
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; Glucose metabolism; Insulin signaling; Streptozotocin; CENTRAL-NERVOUS-SYSTEM; ACTIVATED PROTEIN-KINASE; GROWTH-FACTOR EXPRESSION; ADULT-RAT BRAIN; ALPHA-KETOGLUTARATE DEHYDROGENASE; RECEPTOR SIGNAL-TRANSDUCTION; CEREBRAL GLUCOSE-METABOLISM; GLYCOGEN-SYNTHASE KINASE-3; TRANSGENIC MOUSE MODEL; NITRIC-OXIDE SYNTHASE;
D O I
10.1016/j.arr.2011.01.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Severe abnormalities in brain glucose/energy metabolism and insulin signaling have been documented to take a pivotal role in early sporadic Alzheimer's disease (sAD) pathology. Indeed, the "insulin-resistant brain state" has been hypothesized to form the core of the neurodegenerative events that occur in sAD. In this vein, intracerebroventricular administration of subdiabetogenic doses of streptozotocin (STZ) in rats can induce an insulin-resistant brain state, which is proposed as a suitable experimental model of sAD. This review highlights the involvement of disturbed brain insulin metabolism in sAD etiopathogenesis. Furthermore, current knowledge demonstrates that central STZ administration produces brain pathology and behavioral changes that resemble changes found in sAD patients. The STZ-intracerebroventricularly treated rat represents a promising experimental tool in this field by providing new insights concerning early brain alterations in sAD, which can be translated in novel etiopathogenic and therapeutic approaches in this disease. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:264 / 273
页数:10
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