Visfatin, TNF-α and IL-6 mRNA expression is increased in mononuclear cells from type 2 diabetic women

被引:53
作者
Tsiotra, P. C.
Tsigos, C.
Yfanti, E.
Anastasiou, E.
Vikentiou, M.
Psarra, K.
Papasteriades, C.
Raptis, S. A.
机构
[1] Hellen Natl Ctr Res, Athens, Greece
[2] Alexandra Hosp, Endocrine Sect & Diabet Ctr 1, Athens, Greece
[3] Evangelismos Gen Hosp, Dept Immunol & Histocompatibil, Athens, Greece
关键词
adipokines; visfatin/PBEF; TNF-alpha; type; 2; diabetes; obesity; mRNA expression;
D O I
10.1055/s-2007-990288
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Visfatin, is a new adipokine, highly expressed in the visceral fat of both mice and humans. To examine whether visfatin is expressed in human peripheral monocyte-enriched mononuclear cells and whether its expression is altered in type 2 diabetes (DM2), we compared 24 DM2 women [17 overweight (BMI > 25) and 7 lean (BMI < 25)] to 26 healthy women (14 overweight and 12 lean), all premenopausal. Relative visfatin mRNA levels were significantly higher (approximately 3-fold) in DM2 compared to healthy control women (p < 0.02), independently of the presence of overweight/obesity. Mononuclear TNF-alpha) and IL-6 mRNA expression was also elevated in DM2 compared to control women (p = 0.001 and p = 0.004, respectively), an increase observed in both lean and overweight DM2 women. By contrast, circulating visfatin, TNF-alpha, and IL-6 levels showed no difference between DM2 and control women, while adiponectin plasma levels were significantly decreased in the DM2 women (p < 0.001). Circulating visfatin and TNF-alpha levels did not differ either between the lean and the overweight subgroups of DM2 and control women, while IL-6 plasma levels were significantly higher in both overweight subgroups compared to their lean counterparts. In conclusion, visfatin, TNF-alpha, and IL-6 mRNA expressions are increased in peripheral mononuclear-monocytic cells from women with type 2 diabetes, independent of their BMI, which may enhance the effects of their adipose-derived levels and may contribute to the increased insulin resistance and atherogenic risk of these patients.
引用
收藏
页码:758 / 763
页数:6
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