Department Physiology of Energy Metabolism, German Institute of Human Nutrition Potsdam-Rehbruecke (DIfE), 14558 Nuthetal, Germany.
Department of Nutritional Biochemistry, Faculty of Life Sciences: Food, Nutrition and Health, University of Bayreuth, 95326 Kulmbach, Germany.
Nutrients. 2023 Apr 24;15(9):2052. doi: 10.3390/nu15092052.
Epidemiological studies found that the intake of dairy products is associated with an increased amount of circulating odd-chain fatty acids (OCFA, C15:0 and C17:0) in humans and further indicate that especially C17:0 is associated with a lower incidence of type 2 diabetes. However, causal relationships are not elucidated. To provide a mechanistic link, mice were fed high-fat (HF) diets supplemented with either milk fat or C17:0 for 20 weeks. Cultured primary mouse hepatocytes were used to distinguish differential effects mediated by C15:0 or C17:0. Despite an induction of OCFA after both dietary interventions, neither long-term milk fat intake nor C17:0 supplementation improved diet-induced hepatic lipid accumulation and insulin resistance in mice. HF feeding with milk fat actually deteriorates liver inflammation. Treatment of primary hepatocytes with C15:0 and C17:0 suppressed JAK2/STAT3 signaling, but only C15:0 enhanced insulin-stimulated phosphorylation of AKT. Overall, the data indicate that the intake of milk fat and C17:0 do not mediate health benefits, whereas C15:0 might be promising in further studies.
流行病学研究发现,乳制品的摄入与人体内循环奇数链脂肪酸(OCFA,C15:0 和 C17:0)的含量增加有关,进一步表明 C17:0 与 2 型糖尿病的发病率降低有关。然而,因果关系尚未阐明。为了提供一种机制联系,研究人员用高脂肪(HF)饮食喂养小鼠 20 周,其中补充了牛奶脂肪或 C17:0。培养的原代小鼠肝细胞用于区分 C15:0 或 C17:0 介导的差异作用。尽管两种饮食干预都诱导了 OCFA 的产生,但长期摄入牛奶脂肪或 C17:0 补充剂都不能改善 HF 饮食引起的肝脂肪堆积和胰岛素抵抗。HF 喂养牛奶脂肪实际上会加重肝脏炎症。用 C15:0 和 C17:0 处理原代肝细胞会抑制 JAK2/STAT3 信号通路,但只有 C15:0 增强了胰岛素刺激的 AKT 磷酸化。总的来说,这些数据表明,摄入牛奶脂肪和 C17:0 并不能带来健康益处,而 C15:0 在进一步的研究中可能有希望。