摘要
目的:研究肥胖患者腹部皮下脂肪组织过氧化物酶体增殖物激活受体γ-2(PPARγ2)、瘦素(leptin)、肿瘤坏死因子-α(TNF-α) mRNA与胰岛素抵抗(IR)的关系。方法:应用RT-PCR凝胶成像半定量技术测定男性肥胖患者皮下脂肪组织PPARγ2 mRNA、leptin mRNA及TNF-α mRNA,以及空腹血清leptin、胰岛素(FINS)、空腹血糖(FBS),计算胰岛素抵抗指数(IRI),分析观察指标与肥胖之间的相关关系。结果:①肥胖组FINS、leptin、IRI、脂肪组织mRNA、leptin mRNA及TNF-α mRNA高于非肥胖组(P<0.05);②IRI与leptin mRNA、TNF-α mRNA、PPARγ2 mRNA、leptin、BMI、FINS成正相关(P<0.05);③以IRI为应变量,TNF-α mRNA、PPARγ2 mRNA、leptinmRNA、血清leptin、BMI为自变量做多元逐步回归分析,回归方程:Y=0.358+0.813PPARγ2mRNA。结论:①男性肥胖患者leptin及腹部皮下脂肪组织PPARγ2 mRNA、leptin mRNA、TNF-α mRNA较非肥胖者升高;②男性患者PPARγ2 mRNA与IR密切相关,可以反映IR的程度。
Objective:To study the expression of PPARγ2 mRNA,Leptin mRNA and TNF-α mRNA in subcutaneous adipose tissue of abdomen in obese males and their relationships to insulin resistance.Methods:Fasting serum levels of leptin,insulin,glucose were measured in 17 obese and 21 nonobese subjects. The mRNA expression of PPARγ2,leptin,TNF-α in subcutaneous adipose tissue in the abdomen was quantified in all of subjects by RT-PCR. Insulin resistance index(IRI) was calculated in Homeostasis model assessment HOMA). Then the relationships between them were analyzed.Result:①The fasting serum levels of leptin,insulin and IRI were significantly higher in obese group than in nonobese group(FINS:26.13±13.14 mU/L vs 8.23±3.34 mU/L,P〈0.001; leptin:10.14±4.68 ng/mL vs 5.79±1.66 ng/mL,P〈0.01; IRI:5.43±6.11 vs 1.51±0.84,P〈0.001). The mRNA expression of PPARγ2,leptin and TNF-α in the subcutaneous adipose tissue were significantly higher in obese group than in nonobese group(PPARγ2 mRNA:1.532±0.80 vs 0.96±0.45,P〈0.05; leptin mRNA:1.17±0.73 vs 0.80±0.20 P〈0.05; TNF-α mRNA:1.34±0.60 vs 0.75±0.34;P〈0.001). ②IRI correlated with PPARγ2 mRNA,leptin mRNA,TNF-α mRNA levels,serum levels of leptin and insulin and BMI(P〈0.05); ③PPARγ2 mRNA contributed to the degree of IRI,IRI=0.358+0.813PPARγ2mRNA. Conclusion:The mRNA expression of PPARγ2,leptin,TNF-α in subcutaneous adipose tissue in abdomen were significantly higher in the male obeses.IRI was important factor in influence of the mRNA expression of PPARγ2.
出处
《广西医科大学学报》
CAS
2009年第1期30-33,共4页
Journal of Guangxi Medical University
基金
广西自然科学基金资助项目(No.桂科基0575070)
广西教育厅基金资助项目(99020)