Targeted therapies of the LKB1/AMPK pathway for the treatment of insulin resistance

Eijiro Yamada; Ting Wen A. Lee; Jeffrey E. Pessin; Claire C. Bastie

doi:10.4155/fmc.10.264

Targeted therapies of the LKB1/AMPK pathway for the treatment of insulin resistance

Eijiro Yamada, Ting Wen A. Lee, Jeffrey E. Pessin, Claire C. Bastie

Medicine

Research output: Contribution to journal › Review article › peer-review

13 Scopus citations

Abstract

Type II diabetes is characterized by elevated serum glucose levels and altered lipid metabolism due to peripheral insulin resistance and defects of insulin secretion in the pancreatic -cells. While some cases of obesity and Type II diabetes result from genetic dysfunction, the increased worldwide incidence of these two disorders strongly suggest that the contribution of environmental factors such as sedentary lifestyles and high-calorie intake may disrupt energy balance. AMP-activated protein kinase and its upstream kinase liver kinase B1 are conserved serine/threonine kinases regulating anabolic and catabolic metabolic processes, therefore representing attractive therapeutic targets for the treatment of obesity and Type II diabetes. In this review, we will discuss the advantages of targeting the liver kinase B1/AMP-activated protein kinase pathway for the treatment of metabolic diseases.

Original language	English (US)
Pages (from-to)	1785-1796
Number of pages	12
Journal	Future Medicinal Chemistry
Volume	2
Issue number	12
DOIs	https://doi.org/10.4155/fmc.10.264
State	Published - Dec 2010

ASJC Scopus subject areas

Molecular Medicine
Pharmacology
Drug Discovery

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