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脂肪组织中从头脂肪生成的标志物:与人类小脂肪细胞和胰岛素敏感性的关联。

Markers of de novo lipogenesis in adipose tissue: associations with small adipocytes and insulin sensitivity in humans.

作者信息

Roberts R, Hodson L, Dennis A L, Neville M J, Humphreys S M, Harnden K E, Micklem K J, Frayn K N

机构信息

Oxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Churchill Hospital, Oxford, UK.

出版信息

Diabetologia. 2009 May;52(5):882-90. doi: 10.1007/s00125-009-1300-4. Epub 2009 Feb 28.

Abstract

AIMS/HYPOTHESIS: Previous studies have shown relationships between fatty acid ratios in adipose tissue triacylglycerol (TG), adipocyte size and measures of insulin sensitivity. We hypothesised that variations in adipose tissue de novo lipogenesis (DNL) in relation to adiposity might explain some of these observations.

METHODS

In a cross-sectional study, subcutaneous abdominal adipose tissue biopsies from 59 people were examined in relation to fasting and post-glucose insulin sensitivity. Adipocyte size, TG fatty acid composition and mRNA expression of lipogenic genes were determined.

RESULTS

We found strong positive relationships between adipose tissue TG content of the fatty acids myristic acid (14:0) and stearic acid (18:0) with insulin sensitivity (HOMA model) (p < 0.01 for each), and inverse relationships with adipocyte size (p < 0.01, p < 0.05, respectively). Variation in 18:0 content was the determinant of the adipose tissue TG 18:1 n-9/18:0 ratio, which correlated negatively with insulin sensitivity (p < 0.01), as observed previously. Adipose tissue 18:0 content correlated positively with the mRNA expression of lipogenic genes (e.g. FASN, p < 0.01). Lipogenic gene expression (a composite measure derived from principal components analysis) was inversely correlated with adipocyte cell size (p < 0.001). There was no relationship between dietary saturated fatty acid intake and adipose tissue 18:0 content.

CONCLUSIONS/INTERPRETATION: Our data suggest a physiological mechanism whereby DNL is downregulated as adipocytes expand. Taken together with other data, they also suggest that hepatic and adipose tissue DNL are not regulated in parallel. We also confirm a strong relationship between small adipocytes and insulin sensitivity, which is independent of BMI.

摘要

目的/假设:先前的研究表明,脂肪组织三酰甘油(TG)中的脂肪酸比例、脂肪细胞大小与胰岛素敏感性指标之间存在关联。我们推测,脂肪组织中与肥胖相关的从头脂肪生成(DNL)变化可能解释其中一些观察结果。

方法

在一项横断面研究中,对59人的腹部皮下脂肪组织活检样本进行了检测,分析其与空腹及葡萄糖耐量后胰岛素敏感性的关系。测定了脂肪细胞大小、TG脂肪酸组成及脂肪生成基因的mRNA表达。

结果

我们发现,脂肪酸肉豆蔻酸(14:0)和硬脂酸(18:0)在脂肪组织TG中的含量与胰岛素敏感性(HOMA模型)呈强正相关(均p < 0.01),与脂肪细胞大小呈负相关(分别为p < 0.01和p < 0.05)。18:0含量的变化是脂肪组织TG中18:1 n-9/18:0比例的决定因素,如先前观察到的,该比例与胰岛素敏感性呈负相关(p < 0.01)。脂肪组织18:0含量与脂肪生成基因的mRNA表达呈正相关(如FASN,p < 0.01)。脂肪生成基因表达(通过主成分分析得出的综合指标)与脂肪细胞大小呈负相关(p < 0.001)。膳食饱和脂肪酸摄入量与脂肪组织18:0含量之间无关联。

结论/解读:我们的数据表明存在一种生理机制,即随着脂肪细胞增大,DNL被下调。结合其他数据,还表明肝脏和脂肪组织的DNL调控并非并行。我们还证实了小脂肪细胞与胰岛素敏感性之间存在密切关系,且该关系独立于BMI。

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