Exp Clin Endocrinol Diabetes 2003; 111(4): 191-197
DOI: 10.1055/s-2003-40462
Review

J. A. Barth Verlag in Georg Thieme Verlag Stuttgart · New York

Analysis of Insulin Signaling Pathways through Comparative Genomics. Mapping Mechanisms for Insulin Resistance in Type 2 (Non-Insulin-Dependent) Diabetes Mellitus

S. Lake 1 , A. Krook 2 , J. R. Zierath 2
  • 1Department of Biology, Biovitrum AB, Stockholm, Sweden
  • 2Department of Surgical Sciences, Section for Integrative Physiology at Karolinska Institutet, Stockholm, Sweden
Further Information

Publication History

Received: May 30, 2002 First decision: September 8, 2002

Accepted: October 20, 2002

Publication Date:
07 July 2003 (online)

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Abstract

The precise molecular cause of insulin resistance has not yet been elucidated. Resistance to the normal action of insulin contributes to the pathogenesis of a number of common human disorders, including type 1 (insulin-dependent) and type 2 (non-insulin-dependent) diabetes mellitus, hypertension, and the Metabolic Syndrome X, thus constituting a major public health problem. A disease program aimed at combating this disorder should focus on the identification of targets for therapeutic intervention which may overcome insulin resistance and hence the associated metabolic consequences characteristic of the Metabolic Syndrome. Although the primary defect in the pathogenesis of type 2 diabetes is unknown, genetic and environmental factors are likely to contribute to the manifestation of this progressive metabolic disorder, which is usually not clinically apparent until mid-life. Defects at the level of glucose uptake/phosphorylation characterize insulin resistance in skeletal muscle of type 2 diabetic patients. Identification of putative components of the insulin receptor-signaling pathway may offer insights into mechanisms involved in insulin resistance. Enhanced flux of free fatty acids due to impaired lipid metabolism may contribute to impaired insulin secretion and peripheral insulin resistance. Genes regulating lipolysis are prime candidates for susceptibility towards the metabolic syndrome. Here we describe pathways constituting complex interactions that control glucose homeostasis. We will be considering 1) regulation of glucose uptake by the insulin receptor signaling pathway, and 2) control of adipogenesis and insulin sensitivity by the sterol response element binding protein (SREBP) pathway.

References

Ph.D., Professor of Physiology Juleen R. Zierath

Department of Surgical Sciences and Section for Integrative Physiology
Karolinska Institutet

von Eulers väg 4, II

17177 Stockholm

Sweden

Phone: + 4687287580

Fax: + 46 8 33 54 36

Email: Juleen.Zierath@fyfa.ki.se