Department of Agricultural, Food and Nutritional Science, University of Alberta, Edmonton, Alberta, Canada.
Department of Cell Biology, University of Alberta, Edmonton, Alberta, Canada.
Food Funct. 2024 Sep 30;15(19):9833-9848. doi: 10.1039/d4fo02201g.
: We hypothesized that milk, yogurt, and cheese have differential impacts on energy expenditure (EE) and obesity in mice fed a high-fat diet (HFD). : C57BL/6 mice ( = 16 per group) were fed a HFD or a HFD supplemented with fat-free milk (MILK), fat-free plain yogurt (YOG), or reduced-fat cheddar cheese (CHE; 19 kcal% fat), each provided at 10% of the daily energy intake, for 8 weeks. EE was quantified using a metabolic chamber. Metabolic pathways related to BAT mitochondrial function and uncoupling protein 1 (UCP1) abundance were assessed. Serum lipidomic profiles were analyzed to identify potential mediators of the observed effects. : MILK supplementation lowered weight gain and fat accumulation and enhanced EE and BAT thermogenesis, perhaps the SIRT1-AMPK-PGC1α axis in BAT. This led to elevated UCP1 abundance and enhanced the abundance of hormone-sensitive lipase (HSL). MILK also altered serum lipid species, indicating enhanced energy use, and promoted BAT thermogenesis and mitochondrial function pathways. YOG exhibited a similar pattern but a lower magnitude of effects than MILK on reducing weight gain and fat mass, increasing EE, and BAT thermogenic proteins, including AMPK-PGC1α-UCP1. Both MILK and YOG showed a relative increase in serum PC 15:0_15:0 and LPC 15:0. In contrast, CHE reduced weight gain and increased EE without impacting BAT thermogenesis proteins or serum lipid species. : Our study showed that MILK, YOG, and CHE reduced weight gain in mice on a HFD by increasing EE. MILK and YOG also up-regulated BAT thermogenesis, while both additionally altered lipids involved in fat metabolism and inflammation. CHE did not affect BAT thermogenesis and lipid species compared to HFD.
我们假设牛奶、酸奶和奶酪对高脂肪饮食(HFD)喂养的小鼠的能量消耗(EE)和肥胖有不同的影响。
C57BL/6 小鼠(每组 16 只)喂食 HFD 或 HFD 补充无脂牛奶(MILK)、无脂原味酸奶(YOG)或减脂切达干酪(CHE;脂肪 19%卡路里),每种食物提供 10%的日能量摄入,持续 8 周。使用代谢室定量 EE。评估与 BAT 线粒体功能和解偶联蛋白 1(UCP1)丰度相关的代谢途径。分析血清脂质组学图谱以确定观察到的效应的潜在介质。
MILK 补充降低了体重增加和脂肪堆积,增强了 EE 和 BAT 产热,可能是通过 BAT 中的 SIRT1-AMPK-PGC1α 轴。这导致 UCP1 丰度增加和激素敏感脂肪酶(HSL)丰度增加。MILK 还改变了血清脂质种类,表明能量利用增加,并促进了 BAT 产热和线粒体功能途径。YOG 表现出类似的模式,但在降低体重增加和脂肪量、增加 EE 和 BAT 产热蛋白方面的效果低于 MILK,包括 AMPK-PGC1α-UCP1。MILK 和 YOG 均显示血清 PC 15:0_15:0 和 LPC 15:0 的相对增加。相比之下,CHE 降低了体重增加并增加了 EE,而不影响 BAT 产热蛋白或血清脂质种类。
我们的研究表明,MILK、YOG 和 CHE 通过增加 EE 降低了 HFD 喂养小鼠的体重增加。MILK 和 YOG 还上调了 BAT 产热,同时还另外改变了参与脂肪代谢和炎症的脂质。与 HFD 相比,CHE 对 BAT 产热和脂质种类没有影响。