Stop signs in hippocampal insulin signaling: the role of insulin resistance in structural, functional and behavioral deficits

被引:40
作者
Fadel, Jim R. [1 ]
Reagan, Lawrence P. [1 ,2 ]
机构
[1] Univ South Carolina, Sch Med, Dept Pharmacol Physiol & Neurosci, Columbia, SC 29208 USA
[2] WJB Dorn Vet Affairs Med Ctr, Columbia, SC 29209 USA
基金
美国国家卫生研究院;
关键词
HIGH-FAT-DIET; HIGH SATURATED FAT; OBESE ZUCKER RATS; INTRANASAL INSULIN; COGNITIVE FUNCTION; SYNAPTIC PLASTICITY; IMPROVES MEMORY; SPATIAL MEMORY; ALZHEIMERS-DISEASE; DEPENDENT MEMORY;
D O I
10.1016/j.cobeha.2015.12.004
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
In peripheral tissues insulin activates signaling cascades to facilitate glucose uptake from the blood into tissues like liver, muscle and fat. Although insulin appears to play a minor role in the regulation of glucose uptake in the central nervous system (CNS), insulin is known to play a major role in regulating synaptic plasticity in brain regions like the hippocampus. The concept that insulin regulates hippocampal neuroplasticity is further supported from animal models of type 2 diabetes (T2DM) and Alzheimer's disease (AD). The goal of this review is to provide an overview of these studies, as well as the studies that have examined whether deficits in hippocampal insulin signaling are amenable to intervention strategies.
引用
收藏
页码:47 / 54
页数:8
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