Zhang Qiang, Shen Fei, Shen WenQing, Xia Jie, Wang Jing, Zhao Yu, Zhang Zhe, Sun Yi, Qian Min, Ding ShuZhe
Key Laboratory of Adolescent Health Assessment and Exercise Intervention of Ministry of Education, East China Normal University, Shanghai 200241, People's Republic of China.
School of Physical Education & Health, East China Normal University, Shanghai 200241, People's Republic of China.
Diabetes Metab Syndr Obes. 2020 Nov 6;13:4209-4219. doi: 10.2147/DMSO.S275660. eCollection 2020.
Ketogenic diet (KD) and high-intensity interval training (HIIT) have preclinical benefits for type 2 diabetes (Db). However, the health risks of long-term KD use in diabetes should be ascertained and prevented. We hypothesized that KD-induced liver fibrosis in type 2 diabetic mice could be ameliorated by HIIT.
Streptozotocin-induced type 2 diabetic mice were divided into high-fat diet (HFD) control (Db+HFD+Sed), KD control (Db+KD+Sed), HFD coupled with HIIT (Db+HFD+HIIT), and KD coupled with HIIT (Db+KD+HIIT) groups (n=6, per group). Control mice were kept in sedentary (Sed), while HIIT group mice underwent 40-minute high-intensity interval training three alternate days per week. After 8-week intervention, the indicators of body weight and insulin resistance, oxidative stress markers, hepatic fibrosis, genetic and protein expression of related pathways were tested.
We found that fasting blood glucose level was reduced in the Db+HFD+HIIT, Db+KD+Sed, and Db+KD+HIIT groups. Insulin sensitivity was increased in diabetic mice of these groups, whereas ROS levels were decreased in mice that underwent HIIT. The immunohistochemical staining of liver, serum index, and hepatic parameters of diabetic mice in the KD group revealed liver fibrosis, which was significantly attenuated by HIIT. Besides, these effects of HIIT were the outcome of hepatic stellate cell's inactivation, reduced protein expression of matrix metalloproteinases and tissue inhibitor of metalloproteinases, and the inhibition of TGF-β1/Smad signaling.
KD had a profound fibrotic effect on the liver of type 2 diabetic mice, whereas HIIT ameliorated this effect. KD did not show any apparent benefit as far as glucose tolerance and homeostasis were concerned. Concisely, our results demonstrated that KD should be coupled with HIIT for the prevention and preclinical mitigation of type 2 diabetes.
生酮饮食(KD)和高强度间歇训练(HIIT)对2型糖尿病(Db)具有临床前益处。然而,糖尿病患者长期使用KD的健康风险应予以确定并预防。我们假设HIIT可改善2型糖尿病小鼠中KD诱导的肝纤维化。
将链脲佐菌素诱导的2型糖尿病小鼠分为高脂饮食(HFD)对照组(Db + HFD + Sed)、KD对照组(Db + KD + Sed)、HFD联合HIIT组(Db + HFD + HIIT)和KD联合HIIT组(Db + KD + HIIT)(每组n = 6)。对照小鼠保持久坐(Sed)状态,而HIIT组小鼠每周隔天进行一次40分钟的高强度间歇训练。干预8周后,检测体重和胰岛素抵抗指标、氧化应激标志物、肝纤维化、相关通路的基因和蛋白表达。
我们发现,Db + HFD + HIIT、Db + KD + Sed和Db + KD + HIIT组的空腹血糖水平降低。这些组的糖尿病小鼠胰岛素敏感性增加,而进行HIIT的小鼠ROS水平降低。KD组糖尿病小鼠的肝脏免疫组化染色、血清指标和肝脏参数显示有肝纤维化,HIIT可使其显著减轻。此外,HIIT的这些作用是肝星状细胞失活、基质金属蛋白酶和金属蛋白酶组织抑制剂蛋白表达降低以及TGF-β1/Smad信号通路受抑制的结果。
KD对2型糖尿病小鼠的肝脏有显著的纤维化作用,而HIIT可改善这种作用。就葡萄糖耐量和内环境稳态而言,KD未显示出任何明显益处。简而言之,我们的结果表明,KD应与HIIT联合使用,以预防和临床前减轻2型糖尿病。