The role of SIRT1 in the pathogenesis of insulin resistance in skeletal muscle

被引:5
|
作者
Stefanowicz, Magdalena [1 ]
Straczkowski, Marek [1 ]
Karczewska-Kupczewska, Monika [1 ]
机构
[1] Uniwersytet Med Bialymstoku, Zaklad Chorob Metab, PL-15089 Bialystok, Poland
来源
POSTEPY HIGIENY I MEDYCYNY DOSWIADCZALNEJ | 2015年 / 69卷
关键词
SIRT1; AMPK; insulin resistance; skeletal muscle; ACTIVATED PROTEIN-KINASE; FATTY-ACID OXIDATION; METABOLIC SYNDROME; LIPID-METABOLISM; GENE-EXPRESSION; PGC-1-ALPHA; AMPK; MECHANISMS; SIRTUINS; GLUCOSE;
D O I
10.5604/17322693.1136379
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Skeletal muscle insulin resistance manifests as a decreased ability of insulin to stimulate glucose uptake in consequence of an impairment in its intracellular signaling. Sirtuin 1 (SIRT1), which belongs to the family of sirtuins (Sir2; silent information regulator 2 protein) participates in the regulation of skeletal muscle glucose and lipid metabolism. Experimental studies indicate that SIRT1 may play a role in the pathogenesis of skeletal muscle insulin resistance. SIRT1 directly influences insulin signal transduction pathway. It increases insulin-dependent IRS2 phosphorylation and Akt activation. Moreover, SIRT1 interacts with PGC1a and AMPK to stimulate muscle glucose uptake and fatty acid oxidation and thus it can prevent insulin resistance. SIRT1 activators might be useful in the treatment of insulin resistance-related diseases.
引用
收藏
页码:63 / 68
页数:6
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