Loss of resistin improves glucose homeostasis in leptin deficiency

被引:122
作者
Qi, Yong
Nie, Zhenying
Lee, Yun-Sik
Singhal, Neel S.
Scherer, Philipp E.
Lazar, Mitchell A.
Ahima, Rexford S.
机构
[1] Univ Penn, Sch Med, Div Endocrinol Diabet & Metab, Philadelphia, PA 19104 USA
[2] Inst Diabet Obes & Metab, Philadelphia, PA USA
[3] Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10467 USA
[4] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
关键词
INSULIN-RESISTANCE; SKELETAL-MUSCLE; RECOMBINANT RESISTIN; BODY-WEIGHT; OBESITY; EXPRESSION; METABOLISM; ROSIGLITAZONE; SENSITIVITY; ADIPOCYTES;
D O I
10.2337/db05-0615
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Resistin levels are increased in obesity, and hyperresistinemia impairs glucose homeostasis in rodents. Here, we have determined the role of resistin in ob/ob mice that are obese and insulin resistant because of genetic deficiency of leptin. Loss of resistin increased obesity in ob/ob mice by further lowering the metabolic rate without affecting food intake. Nevertheless, resistin deficiency improved glucose tolerance and insulin sensitivity in these severely obese mice, largely by enhancing insulin-mediated glucose disposal in muscle and adipose tissue. In contrast, in C57BL/6J mice with diet-induced obesity but wild-type leptin alleles, resistin deficiency reduced hepatic glucose production and increased peripheral glucose uptake. Resistin deficiency enhanced Akt phosphorylation in muscle and liver and decreased suppressor of cytokine signaling-3 level in muscle, and these changes were reversed by resistin replacement. Together, these results provide strong support for an important role of resistin in insulin resistance and diabetes associated with genetic or diet-induced obesity.
引用
收藏
页码:3083 / 3090
页数:8
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