Richardson Dawn K, Kashyap Sangeeta, Bajaj Mandeep, Cusi Kenneth, Mandarino Steven J, Finlayson Jean, DeFronzo Ralph A, Jenkinson Christopher P, Mandarino Lawrence J
Division of Diabetes, Department of Medicine, The University of Texas Health Science Center, San Antonio, Texas 78229, USA.
J Biol Chem. 2005 Mar 18;280(11):10290-7. doi: 10.1074/jbc.M408985200. Epub 2004 Dec 14.
The association between elevated plasma free fatty acid (FFA) concentrations and insulin resistance is well known. Although the cause and effect relationship between FFAs and insulin resistance is complex, plasma FFA is negatively correlated with the expression of peroxisome proliferator activated receptor-gamma cofactor-1 (PGC-1) and nuclear encoded mitochondrial genes. To test whether this association is causal, we infused a triglyceride emulsion (or saline as control) into healthy subjects to increase plasma FFA for 48 h followed by muscle biopsies, microarray analysis, quantitative real time PCR, and immunoblots. Lipid infusion increased plasma FFA concentration from 0.48 +/- 0.02 to 1.73 +/- 0.43 mm and decreased insulin-stimulated glucose disposal from 8.82 +/- 0.69 to 6.67 +/- 0.66 mg/kg.min, both with p < 0.05. PGC-1 mRNA, along with mRNAs for a number of nuclear encoded mitochondrial genes, were reduced by lipid infusion (p < 0.05). Microarray analysis also revealed that lipid infusion caused a significant overexpression of extracellular matrix genes and connective tissue growth factor. Quantitative reverse transcription PCR showed that the mRNA expression of collagens and multiple extracellular matrix genes was higher after the lipid infusion (p < 0.05). Immunoblot analysis revealed that lipid infusion also increased the expression of collagens and the connective tissue growth factor protein. These data suggest that an experimental increase in FFAs decreases the expression of PGC-1 and nuclear encoded mitochondrial genes and also increases the expression of extracellular matrix genes in a manner reminiscent of inflammation.
血浆游离脂肪酸(FFA)浓度升高与胰岛素抵抗之间的关联已广为人知。尽管FFA与胰岛素抵抗之间的因果关系很复杂,但血浆FFA与过氧化物酶体增殖物激活受体γ辅激活因子1(PGC-1)及核编码线粒体基因的表达呈负相关。为了验证这种关联是否具有因果性,我们向健康受试者输注甘油三酯乳剂(或生理盐水作为对照)以提高血浆FFA水平48小时,随后进行肌肉活检、微阵列分析、定量实时PCR和免疫印迹。脂质输注使血浆FFA浓度从0.48±0.02毫摩尔升至1.73±0.43毫摩尔,并使胰岛素刺激的葡萄糖处置量从8.82±0.69毫克/千克·分钟降至6.67±0.66毫克/千克·分钟,两者均p<0.05。脂质输注降低了PGC-1 mRNA以及一些核编码线粒体基因的mRNA水平(p<0.05)。微阵列分析还显示,脂质输注导致细胞外基质基因和结缔组织生长因子显著过表达。定量逆转录PCR表明,脂质输注后胶原蛋白和多种细胞外基质基因的mRNA表达更高(p<0.05)。免疫印迹分析显示,脂质输注还增加了胶原蛋白和结缔组织生长因子蛋白的表达。这些数据表明,实验性升高FFA会降低PGC-1和核编码线粒体基因的表达,还会以类似于炎症的方式增加细胞外基质基因的表达。