Adipokines - removing road blocks to obesity and diabetes therapy

被引:200
作者
Blueher, Matthias [1 ]
机构
[1] Univ Leipzig, Dept Med, Liebigstr 20, D-04103 Leipzig, Germany
关键词
Adipokines; Obesity; Type; 2; diabetes; Road blocks; Therapeutic compounds; Leptin; Adiponectin; DPP4; Vaspin; Nampt/visfatin; Nesfatin-1; Apelin; BMP7; NECROSIS-FACTOR-ALPHA; INCREASED INSULIN SENSITIVITY; BONE MORPHOGENETIC PROTEIN-7; ADIPOSE-TISSUE EXPRESSION; DIET-INDUCED OBESITY; WEIGHT-LOSS; RECOMBINANT LEPTIN; LINKING OBESITY; IN-VIVO; ADIPONECTIN;
D O I
10.1016/j.molmet.2014.01.005
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Prevention of obesity and therapeutic weight loss interventions have provided only limited long term success. Therefore there is an urgent need to develop novel pharmacological treatment strategies, which target mechanisms underlying positive energy balance, excessive fat accumulation and adverse fat distribution. Adipokines may have potential for future pharmacological treatment strategies of obesity and metabolic diseases, because they are involved in the regulation of appetite and satiety, energy expenditure, endothelial function, blood pressure, insulin sensitivity, adipogenesis, fat distribution and insulin secretion and others. There are important road blocks on the way from an adipokine candidate to the clinical use a therapeutic compound. Such road blocks include an incomplete understanding of the mechanism of action, resistance to a specific adipokine, side effects of the adipokine and others. This review focuses on the potential of selected adipokines as therapeutic tools or targets and discusses important road blocks, which currently prevent their clinical use. (C) 2014 The Author. Published by Elsevier GmbH. open access under CCBY-NC-SA license
引用
收藏
页码:230 / 240
页数:11
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