Ambery Ashley G, Tackett Lixuan, Penque Brent A, Brozinick Joseph T, Elmendorf Jeffrey S
Department of Cellular and Integrative Physiology, Indiana University School of Medicine, Indianapolis, Indiana.
Center for Diabetes Metabolic Disease Indiana University School of Medicine, Indianapolis, Indiana.
Physiol Rep. 2017 Aug;5(16). doi: 10.14814/phy2.13363.
Insulin action and glucose disposal are enhanced by exercise, yet the mechanisms involved remain imperfectly understood. While the causes of skeletal muscle insulin resistance also remain poorly understood, new evidence suggest excess plasma membrane (PM) cholesterol may contribute by damaging the cortical filamentous actin (F-actin) structure essential for GLUT4 glucose transporter redistribution to the PM upon insulin stimulation. Here, we investigated whether PM cholesterol toxicity was mitigated by exercise. Male C57BL/6J mice were placed on low-fat (LF, 10% kCal) or high-fat (HF, 45% kCal) diets for a total of 8 weeks. During the last 3 weeks of this LF/HF diet intervention, all mice were familiarized with a treadmill for 1 week and then either sham-exercised (0 m/min, 10% grade, 50 min) or exercised (13.5 m/min, 10% grade, 50 min) daily for 2 weeks. HF-feeding induced a significant gain in body mass by 3 weeks. Sham or chronic exercise did not affect food consumption, water intake, or body mass gain. Prior to sham and chronic exercise, "pre-intervention" glucose tolerance tests were performed on all animals and demonstrated that HF-fed mice were glucose intolerant. While sham exercise did not affect glucose tolerance in the LF or HF mice, exercised mice showed an improvement in glucose tolerance. Muscle from sham-exercised HF-fed mice showed a significant increase in PM cholesterol, loss of cortical F-actin, and decrease in insulin-stimulated glucose transport compared to sham-exercised LF-fed mice. These HF-fed skeletal muscle membrane/cytoskeletal abnormalities and insulin resistance were improved in exercised mice. These data reveal a new therapeutic aspect of exercise being regulation of skeletal muscle PM cholesterol homeostasis. Further studies on this mechanism of insulin resistance and the benefits of exercise on its prevention are needed.
运动可增强胰岛素作用和葡萄糖代谢,但其中涉及的机制仍未完全明了。虽然骨骼肌胰岛素抵抗的成因也尚不清楚,但新证据表明,过量的质膜(PM)胆固醇可能通过破坏皮质丝状肌动蛋白(F-肌动蛋白)结构而导致胰岛素抵抗,这种结构对于胰岛素刺激时GLUT4葡萄糖转运体重新分布到质膜至关重要。在此,我们研究了运动是否能减轻质膜胆固醇毒性。将雄性C57BL/6J小鼠分为低脂(LF,10%千卡)或高脂(HF,45%千卡)饮食组,共喂养8周。在LF/HF饮食干预的最后3周,所有小鼠在跑步机上适应1周,然后每天进行假运动(0米/分钟,10%坡度,50分钟)或运动(13.5米/分钟,10%坡度,50分钟),持续2周。到第3周时,高脂喂养使体重显著增加。假运动或长期运动对食物消耗、水摄入或体重增加均无影响。在假运动和长期运动前,对所有动物进行“干预前”葡萄糖耐量试验,结果显示高脂喂养的小鼠存在葡萄糖不耐受。虽然假运动对低脂或高脂小鼠的葡萄糖耐量没有影响,但运动小鼠的葡萄糖耐量有所改善。与假运动的低脂喂养小鼠相比,假运动的高脂喂养小鼠的肌肉显示质膜胆固醇显著增加、皮质F-肌动蛋白减少以及胰岛素刺激的葡萄糖转运降低。运动小鼠的这些高脂喂养骨骼肌膜/细胞骨架异常和胰岛素抵抗得到改善。这些数据揭示了运动在调节骨骼肌质膜胆固醇稳态方面的新治疗作用。需要进一步研究这种胰岛素抵抗机制以及运动对其预防的益处。