Dotzert Michelle S, Murray Michael R, McDonald Matthew W, Olver T Dylan, Velenosi Thomas J, Hennop Anzel, Noble Earl G, Urquhart Brad L, Melling C W James
Exercise Biochemistry Laboratory, School of Kinesiology, Western University, London, Ontario, Canada.
Neurovascular Research Laboratory, School of Kinesiology, Western University, London, Ontario, Canada.
Sci Rep. 2016 May 20;6:26379. doi: 10.1038/srep26379.
The etiology of insulin resistance in Type 1 Diabetes (T1D) is unknown, however it affects approximately 20% of T1D patients. Intramyocellular lipids (IMCL) have been identified as a mechanism of insulin resistance. We examined skeletal muscle of T1D rats to determine if alterations in lipid metabolism were evident and whether aerobic exercise training improves IMCL and insulin resistance. To do so, 48 male Sprague-Dawley rats were divided into control (C), sedentary diabetes (D) and diabetes exercise (DX) groups. Following multiple low-dose Streptozotocin (STZ) injections (20 mg/kg), glycemia (9-15 mM) was maintained using insulin treatment. DX were treadmill trained at high intensity (~75% V02max; 5days/week) for 10 weeks. The results demonstrate that D exhibited insulin resistance compared with C and DX, indicated by decreased glucose infusion rate during a hyperinsulinemic-euglycemic clamp (p < 0.05). There were no differences between C and DX, suggesting that exercise improved insulin resistance (p < 0.05). Metabolomics analysis revealed a significant shift in lipid metabolism whereby notable fatty acid metabolites (arachidonic acid, palmitic acid and several polyunsaturated fatty acids) were significantly elevated in D compared to C and DX. Based on the intermediates observed, insulin resistance in T1D is characterized by an insulin-desensitizing intramyocellular fatty acid metabolite profile that is ameliorated with exercise training.
1型糖尿病(T1D)中胰岛素抵抗的病因尚不清楚,然而它影响了约20%的T1D患者。细胞内脂质(IMCL)已被确定为胰岛素抵抗的一种机制。我们检查了T1D大鼠的骨骼肌,以确定脂质代谢是否有明显改变,以及有氧运动训练是否能改善IMCL和胰岛素抵抗。为此,将48只雄性Sprague-Dawley大鼠分为对照组(C)、久坐糖尿病组(D)和糖尿病运动组(DX)。在多次低剂量链脲佐菌素(STZ)注射(20mg/kg)后,使用胰岛素治疗维持血糖水平(9-15mM)。DX组在跑步机上进行高强度训练(约75%最大摄氧量;每周5天),持续10周。结果表明,与C组和DX组相比,D组表现出胰岛素抵抗,这在高胰岛素-正常血糖钳夹期间葡萄糖输注速率降低中得到体现(p<0.05)。C组和DX组之间没有差异,表明运动改善了胰岛素抵抗(p<0.05)。代谢组学分析显示脂质代谢发生了显著变化,与C组和DX组相比,D组中显著的脂肪酸代谢物(花生四烯酸、棕榈酸和几种多不饱和脂肪酸)显著升高。基于观察到的中间产物,T1D中的胰岛素抵抗的特征是细胞内脂肪酸代谢物谱使胰岛素脱敏,而运动训练可改善这种情况。