Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.
PLoS One. 2013 Aug 12;8(8):e71747. doi: 10.1371/journal.pone.0071747. eCollection 2013.
Diet-induced obesity is a rising health concern which can lead to the development of glucose intolerance and muscle insulin resistance and, ultimately, type II diabetes mellitus. This research investigates the associations between glucose intolerance or muscle insulin resistance and tissue specific changes during the progression of diet-induced obesity.
C57BL/6J mice were fed a normal or high-fat diet (HFD; 60% kcal fat) for 3 or 8 weeks. Disease progression was monitored by measurements of body/tissue mass changes, glucose and insulin tolerance tests, and ex vivo glucose uptake in intact muscles. Lipid metabolism was analyzed using metabolic chambers and ex vivo palmitate assays in intact muscles. Skeletal muscle, liver and adipose tissues were analyzed for changes in inflammatory gene expression. Plasma was analyzed for insulin levels and inflammatory proteins. Histological techniques were used on muscle and liver cryosections to assess metabolic and morphological changes.
PRINCIPAL FINDINGS/CONCLUSIONS: A rapid shift in whole body metabolism towards lipids was observed with HFD. Following 3 weeks of HFD, elevated total lipid oxidation and an oxidative fiber type shift had occurred in the skeletal muscle, which we propose was responsible for delaying intramyocellular lipid accumulation and maintaining muscle's insulin sensitivity. Glucose intolerance was present after three weeks of HFD and was associated with an enlarged adipose tissue depot, adipose tissue inflammation and excess hepatic lipids, but not hepatic inflammation. Furthermore, HFD did not significantly increase systemic or muscle inflammation after 3 or 8 weeks of HFD suggesting that early diet-induced obesity does not cause inflammation throughout the whole body. Overall these findings indicate skeletal muscle did not contribute to the development of HFD-induced impairments in whole-body glucose tolerance following 3 weeks of HFD.
饮食诱导的肥胖是一个日益严重的健康问题,可导致葡萄糖耐量受损和肌肉胰岛素抵抗,并最终导致 2 型糖尿病。本研究调查了在饮食诱导肥胖进展过程中,葡萄糖耐量受损或肌肉胰岛素抵抗与组织特异性变化之间的关系。
C57BL/6J 小鼠分别用正常饮食或高脂肪饮食(HFD;60%热量来自脂肪)喂养 3 或 8 周。通过测量体重/组织质量变化、葡萄糖和胰岛素耐量试验以及完整肌肉中的体外葡萄糖摄取来监测疾病进展。使用代谢室和完整肌肉中的体外棕榈酸测定来分析脂质代谢。分析骨骼肌、肝脏和脂肪组织中炎症基因表达的变化。分析血浆中的胰岛素水平和炎症蛋白。使用肌肉和肝脏冷冻切片的组织学技术评估代谢和形态变化。
主要发现/结论:用 HFD 喂养后,观察到全身代谢迅速向脂质转移。用 HFD 喂养 3 周后,骨骼肌中的总脂质氧化和氧化纤维型转变增加,我们认为这是延迟肌内脂质积累和维持肌肉胰岛素敏感性的原因。用 HFD 喂养 3 周后出现葡萄糖耐量受损,与脂肪组织库增大、脂肪组织炎症和肝脏脂质过多有关,但与肝脏炎症无关。此外,用 HFD 喂养 3 或 8 周后,全身或肌肉炎症并未显著增加,这表明早期饮食诱导的肥胖不会导致全身炎症。综上所述,这些发现表明,在 HFD 喂养 3 周后,骨骼肌不会导致 HFD 诱导的全身葡萄糖耐量受损的发展。