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Amelioration of insulin resistance by rosiglitazone is associated with increased adipose cell size in obese type 2 diabetic patients

机译:罗格列酮改善胰岛素抵抗与肥胖2型糖尿病患者脂肪细胞大小增加有关。

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摘要

Early studies reported that the size of adipose cells positively correlates with insulin resistance, but recent evidence suggests that the relationship between adipose cell size and insulin resistance is more complex. We previously reported that among BMI-matched moderately obese subjects who were either insulin sensitive or resistant insulin resistance correlated with the proportion of small adipose cells, rather than the size of the large adipose cells, whereas the size of large adipose cells was found to be a predictor of insulin resistance in the first-degree relatives of type 2 diabetic (T2D) patients. The relationship between adipose cellularity and insulin resistance thus appears to depend on the metabolic state of the individual. We did a longitudinal study with T2D patients treated with the insulin-sensitizer rosiglitazone to test the hypothesis that improved insulin sensitivity is associated with increased adipocyte size. Eleven T2D patients were recruited and treated with rosiglitazone for 90 days. Blood samples and needle biopsies of abdominal subcutaneous fat were taken at six time points and analyzed for cell size distributions. Rosiglitazone treatment ameliorated insulin resistance as evidenced by significantly decreased fasting plasma glucose and increased index of insulin sensitivity, QUICKI. In association with this, we found significantly increased size of the large adipose cells and, with a weaker effect, increased proportion of small adipose cells. We conclude rosiglitazone treatment both enlarges existing large adipose cells and recruits new small adipose cells in T2D patients, improving fat storage capacity in adipose tissue and thus systemic insulin sensitivity.
机译:早期研究报道,脂肪细胞的大小与胰岛素抵抗呈正相关,但最近的证据表明脂肪细胞的大小与胰岛素抵抗之间的关系更为复杂。我们以前曾报道过,在BMI匹配的中度肥胖受试者中,胰岛素敏感性或胰岛素抵抗性与小脂肪细胞的比例而不是大脂肪细胞的大小相关,而大脂肪细胞的大小与2型糖尿病(T2D)患者一级亲属中胰岛素抵抗的预测因子。因此,脂肪细胞性和胰岛素抵抗之间的关系似乎取决于个体的代谢状态。我们对接受胰岛素增敏剂罗格列酮治疗的T2D患者进行了纵向研究,以检验以下假设:胰岛素敏感性提高与脂肪细胞大小增加有关。招募了11名T2D患者并接受罗格列酮治疗90天。在六个时间点采集血液样本和腹部皮下脂肪的穿刺活检,并分析细胞大小分布。罗格列酮治疗改善了胰岛素抵抗,如空腹血糖明显降低和胰岛素敏感性指数QUICKI升高所证明。与此相关的是,我们发现大型脂肪细胞的大小显着增加,而较小脂肪细胞的比例却增加了,但效果却较弱。我们得出结论,罗格列酮治疗既可以扩大现有的大型脂肪细胞,又可以在T2D患者中募集新的小型脂肪细胞,从而提高脂肪在脂肪组织中的储存能力,从而改善系统性胰岛素敏感性。

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