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Expression of Peroxisome Proliferator―Activated Receptor-γ_1 and Peroxisome Proliferator―Activated Receptor-γ_2 in Visceral and Subcutaneous Adipose Tissue of Obese Women

机译:肥胖女性内脏和皮下脂肪组织中过氧化物酶体增殖物活化受体γ_1和过氧化物酶体增殖物活化受体γ_2的表达

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Data regarding the expression of peroxisome proliferator―activated receptor (PPAE)-γ_1 and PPAR-γ_2 in human visceral adipose tissue (VAT) and subcutaneous adipose tissue (SAT) are conflicting. To clarify this issue, we studied 50 women who had a BMI >35 kg/m~2 were undergoing gastric reduction surgery. Phenotyp-ing included recording of anthropometric parameters and of a biological profile. Quantification of the expression of PPAR-γ_1 and PPAR-γ_2 in samples of VAT and SAT was performed by real-time RT-PCR. In both SAT and VAT, the level of expression of PPAR-γ_2 were > 20-fold that of PPAR-γ_1 (P < 0.001 for both). However, only PPAR-γ_1 was differentially expressed, its levels in SAT being 216 +- 34% those in VAT (P < 0.001). In a stepwise, multivariate regression analysis, the levels of PPAR-γ_1 in both SAT and VAT were the major determinants of waist circumference (R~2 = 21% for both; P < 0.01). Finally, leptin but not PPARs appeared as the single parameter explaining the largest part of the variability of BMI in our cohort of patients (R~2 = 22%, P < 0.001). These results are consistent with the putative roles of PPAR-γ_1 and PPAR-γ_2 in carbohydrate metabolism and energy homeostasis, respectively. As such, they constitute an important step toward the identification of potential targets for novel therapeutic strategies in the fields of obesity.
机译:关于人内脏脂肪组织(VAT)和皮下脂肪组织(SAT)中过氧化物酶体增殖物激活受体(PPAE)-γ_1和PPAR-γ_2表达的数据存在矛盾。为了澄清这个问题,我们研究了50名BMI> 35 kg / m〜2的妇女进行胃减少手术。表型包括记录人体测量学参数和生物学特征。通过实时RT-PCR对VAT和SAT样品中PPAR-γ_1和PPAR-γ_2的表达进行定量。在SAT和增值税中,PPAR-γ_2的表达水平是PPAR-γ_1的20倍以上(两者均P <0.001)。然而,仅PPAR-γ_1被差异表达,其在SAT中的水平是在VAT中的216±34%(P <0.001)。在逐步多元回归分析中,SAT和增值税中PPAR-γ_1的水平是腰围的主要决定因素(两者的R〜2 = 21%; P <0.01)。最后,瘦素而不是PPARs作为单一参数解释了我们患者队列中BMI变异的最大部分(R〜2 = 22%,P <0.001)。这些结果与PPAR-γ_1和PPAR-γ_2分别在碳水化合物代谢和能量稳态中的假定作用相一致。这样,它们构成了朝着识别肥胖领域新治疗策略的潜在靶标迈出的重要一步。

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