Top Institute Food and Nutrition, Wageningen, The Netherlands.
PLoS One. 2011 Jan 14;6(1):e14503. doi: 10.1371/journal.pone.0014503.
The involvement of muscle triacylglycerol (TAG) storage in the onset of insulin resistance is questioned and the attention has shifted towards inhibition of insulin signalling by the lipid intermediate diacylglycerol (DAG). The enzyme 1,2-acylCoA:diacylglyceroltransferase-1 (DGAT1) esterifies a fatty acyl-CoA on DAG to form TAG. Therefore, the aim of the present study was to investigate if unilateral overexpression of DGAT1 in adult rat Tibialis anterior (TA) muscle will increase conversion of the lipid intermediate DAG into TAG, thereby improving muscle insulin sensitivity.
METHODOLOGY/PRINCIPAL FINDINGS: The DGAT1 gene construct was injected in the left TA muscle of male rats on chow or high-fat (45% kcal) diet for three weeks, followed by application of one 800 V/cm and four 80 V/cm pulses, using the contralateral leg as sham-electroporated control. Seven days after electroporation, muscle specific insulin sensitivity was assessed with a hyperinsulinemic euglycemic clamp using 2-deoxy-[3H]glucose. Here, we provide evidence that unilateral overexpression of DGAT1 in TA muscle of male rats is associated with an increased rather than decreased DAG content. Strikingly, this increase in DAG content was accompanied by improved muscle insulin sensitivity. Interestingly, markers of muscle lipolysis and mitochondrial function were also increased in DGAT1 overexpressing muscle.
CONCLUSIONS/SIGNIFICANCE: We conclude that unilateral DGAT1 overexpression can rescue insulin sensitivity, possibly by increasing DAG and TAG turnover in skeletal muscle. In case of a proper balance between the supply and oxidation of fatty acids in skeletal muscle, the lipid intermediate DAG may not exert harmful effects on insulin signalling.
肌肉三酰基甘油(TAG)储存是否参与胰岛素抵抗的发生受到质疑,人们的注意力已经转移到脂质中间产物二酰基甘油(DAG)抑制胰岛素信号传导上。1,2-酰基辅酶 A:二酰基甘油转移酶-1(DGAT1)将脂肪酸辅酶 A 酯化到 DAG 上形成 TAG。因此,本研究的目的是研究在成年大鼠比目鱼肌(TA)中单侧过表达 DGAT1 是否会增加脂质中间产物 DAG 转化为 TAG,从而提高肌肉胰岛素敏感性。
方法/主要发现:将 DGAT1 基因构建体注射到雄性大鼠的左侧 TA 肌肉中,在正常饮食或高脂肪(45%卡路里)饮食下进行了三周,然后使用对侧腿作为假电穿孔对照,施加一个 800 V/cm 和四个 80 V/cm 的脉冲。电穿孔 7 天后,使用 2-脱氧-[3H]葡萄糖进行高胰岛素-正常血糖钳夹来评估肌肉特异性胰岛素敏感性。在这里,我们提供的证据表明,雄性大鼠 TA 肌肉中 DGAT1 的单侧过表达与 DAG 含量的增加而不是减少有关。引人注目的是,这种 DAG 含量的增加伴随着肌肉胰岛素敏感性的提高。有趣的是,DGAT1 过表达肌肉中的肌肉脂解和线粒体功能标志物也增加了。
结论/意义:我们得出结论,单侧 DGAT1 过表达可以挽救胰岛素敏感性,可能是通过增加骨骼肌中 DAG 和 TAG 的周转率来实现的。在骨骼肌中脂肪酸供应和氧化之间保持适当平衡的情况下,脂质中间产物 DAG 可能不会对胰岛素信号传导产生有害影响。