Zhang Qiang, Xu Lingyan, Xia Jie, Wang Dongmei, Qian Min, Ding Shuzhe
Key Laboratory of Adolescent Health Assessment and Exercise Intervention, Ministry of Education, East China Normal University, Shanghai 200241, China.
School of Physical Education & Health Care, East China Normal University, Shanghai 200241, China.
PPAR Res. 2018 Mar 20;2018:4827643. doi: 10.1155/2018/4827643. eCollection 2018.
Type 2 diabetes is a prevalent chronic disease arising as a serious public health problem worldwide. Diet intervention is considered to be a critical strategy in glycemic control of diabetic patients. Recently, the low-carbohydrate ketogenic diet is shown to be effective in glycemic control and weight loss. However, hepatic lipid accumulation could be observed in mice treated with ketogenic diet. On the other hand, exercise is a well-known approach for treating nonalcoholic fatty liver disease. We thus hypothesize that the combination of ketogenic diet and exercise could improve insulin sensitivity, while minimizing adverse effect of hepatic steatosis. In order to test this hypothesis, we established diabetic mice model with streptozotocin (STZ) and divided them into control group, ketogenic diet group, and ketogenic diet with aerobic exercise group. We found that after six weeks of intervention, mice treated with ketogenic diet and ketogenic diet combined with exercise both have lower body weights, HbAlc level, HOMA index, and improvements in insulin sensitivity, compared with diabetes group. In addition, mice in ketogenic diet intervention exhibited hepatic steatosis shown by serum and hepatic parameters, as well as histochemistry staining in the liver, which could be largely relieved by exercise. Furthermore, gene analysis revealed that ketogenic diet in combination with exercise reduced PPAR and lipid synthetic genes, as well as enhancing PPAR and lipid -oxidation gene program in the liver compared to those in ketogenic diet without exercise. Overall, the present study demonstrated that the combination of ketogenic diet and a moderate-intensity aerobic exercise intervention improved insulin sensitivity in diabetic mice, while avoiding hepatic steatosis, which provided a novel strategy in the combat of diabetes.
2型糖尿病是一种普遍存在的慢性疾病,已成为全球严重的公共卫生问题。饮食干预被认为是糖尿病患者血糖控制的关键策略。最近,低碳水化合物生酮饮食已被证明在血糖控制和体重减轻方面有效。然而,在用生酮饮食治疗的小鼠中可观察到肝脏脂质积累。另一方面,运动是治疗非酒精性脂肪性肝病的一种众所周知的方法。因此,我们假设生酮饮食和运动相结合可以提高胰岛素敏感性,同时将肝脂肪变性的不良影响降至最低。为了验证这一假设,我们用链脲佐菌素(STZ)建立了糖尿病小鼠模型,并将它们分为对照组、生酮饮食组和生酮饮食加有氧运动组。我们发现,经过六周的干预,与糖尿病组相比,接受生酮饮食和生酮饮食加运动治疗的小鼠体重、糖化血红蛋白水平、稳态模型评估指数均较低,胰岛素敏感性也有所改善。此外,生酮饮食干预组的小鼠通过血清和肝脏参数以及肝脏组织化学染色显示出肝脂肪变性,而运动可以在很大程度上缓解这种情况。此外,基因分析显示,与未运动的生酮饮食组相比,生酮饮食与运动相结合可降低肝脏中的过氧化物酶体增殖物激活受体(PPAR)和脂质合成基因,同时增强PPAR和脂质氧化基因程序。总体而言,本研究表明,生酮饮食与中等强度有氧运动干预相结合可提高糖尿病小鼠的胰岛素敏感性,同时避免肝脂肪变性,这为对抗糖尿病提供了一种新策略。