Regulation of glucose transport in human skeletal muscle

被引:81
作者
Koistinen, HA
Zierath, JR
机构
[1] Karolinska Inst, Karolinska Hosp, Dept Clin Physiol, S-10401 Stockholm, Sweden
[2] Univ Helsinki, Cent Hosp & Biomedicum, Dept Med, Div Cardiol, Helsinki, Finland
关键词
AMPK; exercise; glucose transport; insulin resistance; insulin signalling; obesity;
D O I
10.1080/078538902321012351
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Glucose transport, the rate limiting step in glucose metabolism in skeletal muscle, is mediated by insulin-sensitive glucose transporter 4 (GLUT4) and can be activated in skeletal muscle by two separate and distinct signalling pathways: one stimulated by insulin and the second by muscle contractions. Skeletal muscle is the principal tissue responsible for insulin-stimulated glucose disposal and thus the major site of peripheral insulin resistance. Impaired glucose transport in skeletal muscle leads to impaired whole body glucose uptake, and contributes to the pathogenesis of Type 2 diabetes mellitus. A combination of genetic and environmental factors is likely to contribute to the pathogenesis of Type 2 diabetes mellitus; however, the primary defect is still unknown. Intense efforts are underway to define the molecular mechanisms that regulate glucose metabolism in insulin sensitive tissues. This review will present our current understanding of mechanisms regulating glucose transport in skeletal muscle in humans. Elucidation of the pathways involved in the regulation of glucose homeostasis will offer insight into the pathogenesis of insulin resistance and Type 2 diabetes mellitus and may lead to the identification of biochemical entry points for drug intervention to improve glucose homeostasis.
引用
收藏
页码:410 / 418
页数:9
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