Neuromuscular Research Center, Department of Biology of Physical Activity, University of Jyväskylä, Jyväskylä, Finland.
LIKES Research Center for Sport and Health Sciences, Jyväskylä, Finland.
Metabolism. 2014 Aug;63(8):1031-40. doi: 10.1016/j.metabol.2014.05.010. Epub 2014 May 27.
The relation between lipid accumulation and influence of exercise on insulin sensitivity is not straightforward. A proper balance between lipid droplet synthesis, lipolysis, and oxidative metabolism would ensure low local intramyocellular fatty acid levels, thereby possibly protecting against lipotoxicity-associated insulin resistance. This study investigated whether the accumulation of triglycerides and lipid droplets in response to high availability of fatty acids after high-fat feeding would parallel the abundance of intramyocellular perilipin proteins, especially PLIN5. The effects on these variables after diet change or voluntary running exercise intervention in skeletal muscle were also investigated.
During a 19-week experiment, C57BL/6J mice were studied in six different groups: low-fat diet sedentary, low-fat diet active, high-fat diet sedentary, high-fat diet active and two groups which were high-fat sedentary for nine weeks, after which divided into low-fat sedentary or low-fat active groups. Myocellular triglyceride concentration and perilipin protein expression levels were assessed.
We show that, concurrently with impaired insulin sensitivity, the expression level of PLIN5 and muscular triglyceride concentration increased dramatically after high-fat diet. These adaptations were reversible after the diet change intervention with no additional effect of exercise.
After high-fat diet, lipid droplets become larger providing more surface area for PLIN5. We suggest that PLIN5 is an important regulator of lipid droplet turnover in altered conditions of fatty acid supply and consumption. Imbalances in lipid droplet metabolism and turnover might lead to lipotoxicity-related insulin resistance.
脂肪堆积与运动对胰岛素敏感性的影响之间的关系并不简单。脂质滴合成、脂肪分解和氧化代谢之间的适当平衡将确保低局部肌内脂肪酸水平,从而可能防止与脂肪毒性相关的胰岛素抵抗。本研究调查了高脂肪喂养后脂肪酸可用性增加时甘油三酯和脂质滴在肌内的积累是否与肌内 perilipin 蛋白(尤其是 PLIN5)的丰度平行。还研究了饮食改变或自愿跑步运动干预对骨骼肌中这些变量的影响。
在为期 19 周的实验中,对 C57BL/6J 小鼠进行了六组不同的研究:低脂饮食静息组、低脂饮食运动组、高脂饮食静息组、高脂饮食运动组以及两组高脂饮食静息 9 周后分为低脂饮食静息或低脂饮食运动组。评估肌细胞甘油三酯浓度和 perilipin 蛋白表达水平。
我们表明,随着胰岛素敏感性受损,高脂肪饮食后 PLIN5 的表达水平和肌肉甘油三酯浓度急剧增加。这些适应在饮食改变干预后是可逆的,运动没有额外的作用。
高脂肪饮食后,脂质滴变得更大,为 PLIN5 提供了更多的表面积。我们认为,PLIN5 是脂肪酸供应和消耗改变条件下脂质滴周转的重要调节因子。脂质滴代谢和周转的失衡可能导致与脂肪毒性相关的胰岛素抵抗。