Tsintzas Kostas, Chokkalingam Kamal, Jewell Kirsty, Norton Luke, Macdonald Ian A, Constantin-Teodosiu Dumitru
Centre for Integrated Systems Biology and Medicine, Institute of Clinical Research, School of Biomedical Sciences, University of Nottingham, Nottingham NG7 2UH, United Kingdom.
J Clin Endocrinol Metab. 2007 Oct;92(10):3967-72. doi: 10.1210/jc.2007-1104. Epub 2007 Jul 24.
We investigated the effect of elevated plasma free fatty acid and insulin concentrations on PDK4 mRNA transcript and protein content and long-chain acyl-coenzyme A accumulation in human skeletal muscle.
On two occasions, 10 healthy men underwent hyperinsulinemic-euglycemic clamps for 6 h with (LIPID) and without (CON) iv Intralipid (20% at 90 ml/h) plus heparin (200 U prime + 600 U/h) infusion.
Glucose disposal was approximately 50% lower at the end of the clamp in the LIPID compared with the CON trial (37.8 +/- 4.4 and 79.6 +/- 4.0 micromol/kg lean mass.min, respectively; P < 0.01). In the LIPID trial, muscle long-chain acyl-coenzyme A concentration increased after 6 h, but not 3 h of lipid infusion (P < 0.01). Muscle PDK4 mRNA, but not protein, was down-regulated by 2-fold within 3 h in both clamps and decreased further (6-fold; P < 0.01) at 6 h in the CON but not the LIPID clamp. The lipid-induced attenuation in the suppression of PDK4 gene expression was not dependent on the activation of the Akt/FOXO3 pathway.
Accumulation of im lipids plays a more important role than impaired activation of Akt-mediated pathways in the regulation of muscle PDK4 gene expression in lipid-induced acute insulin-resistant states.
我们研究了血浆游离脂肪酸和胰岛素浓度升高对人骨骼肌中PDK4 mRNA转录本、蛋白质含量以及长链酰基辅酶A积累的影响。
10名健康男性分两次进行了6小时的高胰岛素-正常血糖钳夹试验,一次(脂质组)静脉输注脂质乳剂(20%,90 ml/h)加肝素(首剂200 U + 600 U/h),另一次(对照组)不输注。
与对照组相比,脂质组钳夹试验结束时葡萄糖处置率降低了约50%(分别为37.8±4.4和79.6±4.0 μmol/kg去脂体重·分钟;P<0.01)。在脂质组试验中,脂质输注6小时后肌肉长链酰基辅酶A浓度升高,但输注3小时后未升高(P<0.01)。在两个钳夹试验中,肌肉PDK4 mRNA在3小时内下调了2倍,在对照组6小时时进一步降低(6倍;P<0.01),而脂质组未降低。脂质诱导的PDK4基因表达抑制减弱不依赖于Akt/FOXO3途径的激活。
在脂质诱导的急性胰岛素抵抗状态下,脂质积累在调节肌肉PDK4基因表达方面比Akt介导的途径激活受损发挥着更重要的作用。