Glycosphingolipids and insulin resistance

被引:84
作者
Langeveld, Mirjam [2 ]
Aerts, Johannes M. F. G. [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Med Biochem K1 110, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Endocrinol & Metab, NL-1105 AZ Amsterdam, Netherlands
关键词
Glycosphingolipids; Insulin resistance; GM3; PLASMA SPHINGOLIPID METABOLISM; I GAUCHER-DISEASE; SKELETAL-MUSCLE; ADIPOSE-TISSUE; CERAMIDE SYNTHESIS; GANGLIOSIDE GM3; FATTY-ACIDS; GLUCOSYLCERAMIDE SYNTHASE; RECEPTOR SUBSTRATE-1; GLUT4; TRANSLOCATION;
D O I
10.1016/j.plipres.2009.03.002
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
Obesity is associated with an increased risk for insulin resistance, a state characterized by impaired responsiveness of liver, muscle and adipose tissue to insulin. One class of lipids involved in the development of insulin resistance are the (glyco)sphingolipids. Ceramide, the most simple sphingolipid, directly inhibits phosphorylation of the insulin signaling mediator Akt/Protein Kinase B. More complex glycosphingolipids, so-called gangliosides, block phosphorylation of the insulin receptor and down-stream signaling, possibly by exclusion of the insulin receptor from specific membrane domains. Pharmacological inhibition of glycosphingolipid synthesis is found to markedly improve insulin sensitivity in rodent models of insulin resistance. Partial glycosphingolipid reduction is well tolerated and may thus offer an attractive new treatment modality for obesity-induced insulin resistance and type 11 diabetes. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:196 / 205
页数:10
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