Adiponectin, driver or passenger on the road to insulin sensitivity?

被引:200
作者
Ye, Risheng
Scherer, Philipp E. [1 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Internal Med, Touchstone Diabet Ctr, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
关键词
Mouse; Human; Ceramide; AMPK; Oligomeric complexes; AdipoR; Insulin sensitivity; CORONARY-HEART-DISEASE; MOLECULAR-WEIGHT ADIPONECTIN; FATTY-ACID OXIDATION; ACTIVATED PROTEIN-KINASE; SKELETAL-MUSCLE; GENE-EXPRESSION; REGULATES ADIPONECTIN; PPAR-GAMMA; T-CADHERIN; IN-VIVO;
D O I
10.1016/j.molmet.2013.04.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Almost 20 years have passed since the first laboratory evidence emerged that an abundant message encoding a protein with homology to the C1q superfamily is highly specifically expressed in adipocytes. At this stage, we refer to this protein as adiponectin. Despite more than 10,000 reports in the literature since its initial description, we seem to have written only the first chapter in the textbook on adiponectin physiology. With every new aspect we learn about adiponectin, a host of new questions arise with respect to the underlying molecular mechanisms. Here, we aim to summarize recent findings in the field and bring the rodent studies that suggest a causal relationship between adiponectin levels in plasma and systemic insulin sensitivity in perspective with the currently available data on the clinical side. (C) 2013 Elsevier GmbH. Open access under CCBY-NC-ND license
引用
收藏
页码:133 / 141
页数:9
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