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Matrix Metalloproteinase-9 Is Increased in Obese Subjects and Decreases in Response to Pioglitazone

机译:肥胖患者中基质金属蛋白酶9升高,对吡格列酮的应答下降

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Context: The study investigated the regulation of matrix metalloproteinases (MMP)-9 in obesity-associated insulin resistance in humans.Objectives: The objectives of the investigation were to study MMP-9 regulation by insulin resistance and pioglitazone treatment in impaired glucose tolerant subjects using adipose tissue biopsies and study the mechanism of MMP-9 regulation by pioglitazone in adipocyte cultures.Research Design: 86 nondiabetic, weight-stable subjects between 21 and 66 yr of age were recruited in a university hospital research center setting. All subjects underwent a sc adipose tissue incisional biopsy from the lower abdominal wall and insulin sensitivity testing using a frequently sampled iv glucose tolerance test. Impaired glucose-tolerant subjects were randomized to receive metformin or pioglitazone for 10 wk. To study the mechanism of MMP-9 regulation in adipocytes, cells were treated with pioglitazone or protein kinase Cα antisense oligomers, and MMP-9 levels were examined.Results: There was a positive correlation between MMP-9 and body mass index (r = 0.40, P < 0.01) and negative correlation between MMP-9 and insulin sensitivity (r = ?0.46, P < 0.001). The improvement in insulin sensitivity from pioglitazone resulted in a 52 ± 0.2% reduction in MMP-9 mRNA. Fractionation of adipose tissue indicated that MMP-9 was mostly in the stromal vascular fraction. Pioglitazone also decreased MMP-9 in 3T3-F442A adipocytes and THP1 macrophages. Coculture of adipocytes with macrophages augmented MMP-9 expression in adipocytes and pioglitazone decreased MMP-9 in both adipocytes and macrophages.Conclusion: These data indicate that MMP-9 is elevated in insulin resistance and is reduced by pioglitazone.
机译:背景:本研究探讨了基质金属蛋白酶(MMP)-9在肥胖相关的人胰岛素抵抗中的调节作用。目的:研究胰岛素抵抗和吡格列酮治疗对糖耐量减低的受试者的MMP-9调节作用。脂肪组织活检和研究吡格列酮在脂肪细胞培养物中对MMP-9的调控机制。研究设计:在大学医院研究中心招募了86名21至66岁之间,体重稳定的非糖尿病受试者。所有受试者均从下腹壁进行了脂肪组织切开活检,并使用频繁采样的静脉葡萄糖耐量试验进行了胰岛素敏感性试验。糖耐量受损的受试者随机分组接受二甲双胍或吡格列酮治疗10周。为了研究脂肪细胞中MMP-9的调控机制,用吡格列酮或蛋白激酶Cα反义寡聚体处理细胞,并检测MMP-9水平。结果:MMP-9与体重指数呈正相关(r = MMP-9与胰岛素敏感性之间呈负相关(r = 0.46,P <0.001),P = 0.40,P <0.01)。吡格列酮对胰岛素敏感性的改善导致MMP-9 mRNA降低52±0.2%。脂肪组织的分级分离表明MMP-9大部分位于基质血管部分。吡格列酮还降低了3T3-F442A脂肪细胞和THP1巨噬细胞中的MMP-9。脂肪细胞与巨噬细胞共培养可增加脂肪细胞和吡格列酮中MMP-9的表达,从而降低脂肪细胞和巨噬细胞中MMP-9的结论。

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