Omentin: A Novel Link Between Inflammation, Diabesity, and Cardiovascular Disease

被引:244
作者
Tan, Bee K. [1 ,2 ]
Adya, Raghu [1 ]
Randeva, Harpal S. [1 ]
机构
[1] Univ Warwick, Clin Sci Res Inst, Warwick Med Sch, Endocrinol & Metab Grp, Coventry CV4 7AL, W Midlands, England
[2] Cambridge Univ Hosp NHS Fdn Trust, Dept Reprod Med & Surg, Addenbrookes Hosp, Cambridge CB2 0QQ, England
关键词
POLYCYSTIC-OVARY-SYNDROME; EPICARDIAL ADIPOSE-TISSUE; FATTY LIVER-DISEASE; METABOLIC SYNDROME; INSULIN-RESISTANCE; GENE-EXPRESSION; PLASMA-LEVELS; IN-VIVO; OBESITY; ADIPONECTIN;
D O I
10.1016/j.tcm.2010.12.002
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Obesity has reached pandemic proportions and is associated with serious cardiometabolic sequealae including insulin resistance, diabetes, dyslipidemia, hypertension, and cardiovascular disease, where adipose tissue-secreted cytokines, that is, adipokines, have been implicated in these processes. Omentin is a novel adipokine preferentially produced by visceral adipose tissue with insulin-sensitizing effects, where circulating levels are decreased in insulin-resistant states, for example, obesity and diabetes. With respect to vascular biology, omentin causes vasodilatation of blood vessels and attenuates C-reactive protein induced angio genesis potentially via the nuclear factor B signaling pathway, a potent proinflammatory signaling pathway. Thus, omen tin may have beneficial effects on the metabolic syndrome and could potentially be used as a biologic marker and/or pharmacologic agent in this respect. (Trends Cardiovasc Med 2010;20:143-148) (C) 2010, Elsevier Inc. All rights reserved.
引用
收藏
页码:143 / 148
页数:6
相关论文
共 39 条
[1]
Omentin plasma levels and gene expression are decreased in obesity [J].
Batista, Celia M. de Souza ;
Yang, Rong-Ze ;
Lee, Mi-Jeong ;
Glynn, Nicole M. ;
Yu, Dao-Zhan ;
Pray, Jessica ;
Ndubuizu, Kelechi ;
Patil, Susheel ;
Schwartz, Alan ;
Kligman, Mark ;
Fried, Susan K. ;
Gong, Da-Wei ;
Shuldiner, Alan R. ;
Pollin, Toni I. ;
McLenithan, John C. .
DIABETES, 2007, 56 (06) :1655-1661
[2]
Insulin resistance and progression to type 1 diabetes in the European Nicotinamide Diabetes Intervention Trial (ENDIT) [J].
Bingley, Polly J. ;
Mahon, Jeffrey L. ;
Gale, Edwin A. M. .
DIABETES CARE, 2008, 31 (01) :146-150
[3]
Omentin-1 and vaspin are present in the fetus and neonate, and perinatal concentrations are similar in normal and growth-restricted pregnancies [J].
Briana, Despina D. ;
Boutsikou, Maria ;
Baka, Stavroula ;
Gourgiotis, Dimitrios ;
Marmarinos, Antonios ;
Liosi, Sofia ;
Hassiakos, Dimitrios ;
Malamitsi-Puchner, Ariadne .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2011, 60 (04) :486-490
[4]
Cai Run-Ce, 2009, Zhonghua Yi Xue Za Zhi, V89, P381
[5]
Effect of acute physiological hyperinsulinemia on gene expression in human skeletal muscle in vivo [J].
Coletta, Dawn K. ;
Balas, Bogdan ;
Chavez, Alberto O. ;
Baig, Muhammad ;
Abdul-Ghani, Muhammad ;
Kashyap, Sangeeta R. ;
Folli, Franco ;
Tripathy, Devjit ;
Mandarino, Lawrence J. ;
Cornell, John E. ;
DeFronzo, Ralph A. ;
Jenkinson, Christopher P. .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2008, 294 (05) :E910-E917
[6]
Insulin inhibits intranuclear nuclear factor κB and stimulates IκB in mononuclear cells in obese subjects:: Evidence for an anti-inflammatory effect? [J].
Dandona, P ;
Aljada, A ;
Mohanty, P ;
Ghanim, H ;
Hamouda, W ;
Assian, E ;
Ahmad, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (07) :3257-3265
[7]
Metabolic syndrome - A comprehensive perspective based on interactions between obesity, diabetes, and inflammation [J].
Dandona, P ;
Aljada, A ;
Chaudhuri, A ;
Mohanty, P ;
Garg, R .
CIRCULATION, 2005, 111 (11) :1448-1454
[8]
De Flines J, 2010, ACTA GASTRO-ENT BELG, V73, P261
[9]
DEGRAUW WJC, 1995, DIABETIC MED, V12, P117
[10]
Increased toll-like receptor (TLR)2 and TLR4 expression in monocytes from patients with type 1 diabetes: Further evidence of a proinflammatory state [J].
Devaraj, Sridevi ;
Dasu, Mohan R. ;
Rockwood, Jason ;
Winter, William ;
Griffen, Steven C. ;
Jialal, Ishwarlal .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2008, 93 (02) :578-583