Section of Molecular Physiology, Department of Nutrition, Exercise, and Sports, Faculty of Science, University of Copenhagen, Copenhagen, Denmark.
FASEB J. 2019 Apr;33(4):5510-5519. doi: 10.1096/fj.201801950R. Epub 2019 Feb 1.
The nicotinamide adenine dinucleotide-dependent deacetylase, sirtuin (SIRT)1, in skeletal muscle is reduced in insulin-resistant states. However, whether this is an initial mechanism responsible for mediating insulin resistance in human skeletal muscle remains to be investigated. Also, SIRT1 acts as a mitochondrial gene transcriptional regulator and is induced by a short-term, high-fat diet (HFD) in human skeletal muscle. Whether saturated or unsaturated fatty acids (FAs) in the diet are important for this is unknown. We subjected 17 healthy, young men to a eucaloric control (Con) diet and 1 of 2 hypercaloric [+75% energy (E%)] HFDs for 3 d enriched in either saturated (Sat) FA (79 E% fat; Sat) or unsaturated FA (78 E% fat; Unsat). After Sat, SIRT1 protein content and activity in skeletal muscle increased ( P < 0.05; ∼40%) while remaining unchanged after Unsat. Whole-body insulin sensitivity and insulin-stimulated leg glucose uptake were reduced ( P < 0.01; ∼20%) to a similar extent compared to Con after both HFDs. We demonstrate a novel FA type-dependent regulation of SIRT1 protein in human skeletal muscle. Moreover, regulation of SIRT1 does not seem to be an initiating factor responsible for mediating insulin resistance in human skeletal muscle.-Fritzen, A. M., Lundsgaard, A.-M., Jeppesen, J. F., Sjøberg, K. A., Høeg, L. D., Deleuran, H. H., Wojtaszewski, J. F. P., Richter, E. A., Kiens, B. Fatty acid type-specific regulation of SIRT1 does not affect insulin sensitivity in human skeletal muscle.
烟酰胺腺嘌呤二核苷酸依赖性去乙酰化酶,组蛋白脱乙酰酶(SIRT)1,在胰岛素抵抗状态下减少。然而,这是否是介导人类骨骼肌胰岛素抵抗的初始机制仍有待研究。此外,SIRT1 作为一种线粒体基因转录调节剂,在人类骨骼肌中被短期高脂肪饮食(HFD)诱导。饮食中的饱和或不饱和脂肪酸(FA)是否对此很重要尚不清楚。我们让 17 名健康的年轻男性接受了热量平衡的对照(Con)饮食和 2 种高热量[+75%能量(E%)] HFD 中的 1 种,3 天内分别富含饱和(Sat)FA(79%脂肪;Sat)或不饱和 FA(78%脂肪;Unsatur)。在 Sat 之后,骨骼肌中的 SIRT1 蛋白含量和活性增加(P<0.05;约 40%),而在 Unsat 后保持不变。与 Con 相比,两种 HFD 后全身胰岛素敏感性和胰岛素刺激的腿部葡萄糖摄取均降低(P<0.01;约 20%)。我们在人类骨骼肌中证明了一种新型 FA 类型依赖性的 SIRT1 蛋白调节。此外,SIRT1 的调节似乎不是介导人类骨骼肌胰岛素抵抗的起始因素。