Lipocalin-2 Deficiency Attenuates Insulin Resistance Associated With Aging and Obesity

被引:275
作者
Law, Ivy K. M. [1 ]
Xu, Aimin [1 ,2 ,3 ]
Lam, Karen S. L. [2 ,3 ]
Berger, Thorsten [4 ]
Mak, Tak W. [4 ]
Vanhoutte, Paul M. [1 ]
Liu, Jacky T. C. [1 ]
Sweeney, Gary [5 ]
Zhou, Mingyan [1 ,2 ,3 ]
Yang, Bo [1 ]
Wang, Yu [1 ,2 ,3 ]
机构
[1] Univ Hong Kong, Dept Pharmacol & Pharm, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, Dept Med, Hong Kong, Hong Kong, Peoples R China
[3] Univ Hong Kong, Ctr Heart Brain Hormone & Healthy Aging, Hong Kong, Hong Kong, Peoples R China
[4] Princess Margaret Hosp, Campbell Family Inst Breast Canc Res, Toronto, ON M4X 1K9, Canada
[5] York Univ, Dept Biol, Toronto, ON M3J 2R7, Canada
关键词
NECROSIS-FACTOR-ALPHA; GELATINASE-ASSOCIATED LIPOCALIN; ADIPOSE-TISSUE; NEUTROPHIL GELATINASE; TNF-ALPHA; MICE; INFLAMMATION; ADIPOCYTES; EXPRESSION; IDENTIFICATION;
D O I
10.2337/db09-1541
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
OBJECTIVE-The proinflammatory cytokines/adipokines produced from adipose tissue act in an autocrine and/or endocrine manner to perpetuate local inflammation and to induce peripheral insulin resistance. The present study investigates whether lipocalin-2 deficiency or replenishment with this adipokine has any impact on systemic insulin sensitivity and the underlying mechanisms. METHODS AND RESULTS-Under conditions of aging or dietary-/genetic-induced obesity, lipocalin-2 knockout (Lcn2-KO) mice show significantly decreased fasting glucose and insulin levels and improved insulin sensitivity compared with their wild-type littermates. Despite enlarged fat mass, inflammation and the accumulation of lipid peroxidation products are significantly attenuated in the adipose tissues of Lcn2-KO mice. Adipose fatty acid composition of these mice varies significantly from that in wild-type animals. The amounts of arachidonic acid (C20:4 n6) are elevated by aging and obesity and are paradoxically further increased in adipose tissue, but not skeletal muscle and liver of Lcn2-KO mice. On the other hand, the expression and activity of 12-lipoxygenase, an enzyme responsible for metabolizing arachidonic acid, and the production of tumor necrosis factor-alpha (TNF-alpha), a critical insulin resistance-inducing factor, are largely inhibited by lipocalin-2 deficiency. Lipocalin-2 stimulates the expression and activity of 12-lipoxygenase and TNF-alpha production in fat. tissues. Cinnamy1-3,4-dihydroxy-alpha-cyanocinnamate (CDC), an arachidonate lipoxygenase inhibitor, prevents TNF-alpha expression induced by lipocalin-2. Moreover, treatment with TNF-alpha neutralization antibody or CDC significantly attenuated the differences of insulin sensitivity between wild-type and Lcn2-KO mice. CONCLUSIONS-Lipocalin-2 deficiency protects mice from developing aging- and obesity-induced insulin resistance largely by modulating 12-lipoxygenase and TNF-alpha levels in adipose tissue. Diabetes 59:872-882, 2010
引用
收藏
页码:872 / 882
页数:11
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