Univ Lyon, CarMeN Laboratory, INSERM U1060, INRA U1397, INSA Lyon, Université Claude Bernard Lyon 1, 69621, Villeurbanne, France.
Univ Lyon, CarMeN Laboratory, INSERM, INRA, INSA Lyon, Université Claude Bernard Lyon 1, 69600, Oullins, France.
Mol Nutr Food Res. 2019 Feb;63(4):e1801078. doi: 10.1002/mnfr.201801078. Epub 2019 Jan 25.
Enhanced adiposity and metabolic inflammation are major features of obesity associated with altered gut microbiota and intestinal barrier. How these metabolic outcomes can be impacted by milk polar lipids (MPL), naturally containing 25% of sphingomyelin, is investigated in mice fed a mixed high-fat (HF) diet .
Male C57Bl/6 mice receive a HF-diet devoid of MPL (21% fat, mainly palm oil, in chow), or supplemented with 1.1% or 1.6% of MPL (HF-MPL1; HF-MPL2) via a total-lipid extract from butterserum concentrate for 8 weeks. HF-MPL2 mice gain less weight versus HF (p < 0.01). Diets do not impact plasma markers of inflammation but in the liver, HF-MPL2 tends to decrease hepatic gene expression of macrophage marker F4/80 versus HF-MPL1 (p = 0.06). Colonic crypt depth is the maximum in HF-MPL2 (p < 0.05). In cecal microbiota, HF-MPL1 increases Bifidobacterium animalis versus HF (p < 0.05). HF-MPL2 decreases Lactobacillus reuteri (p < 0.05), which correlates negatively with the fecal loss of milk sphingomyelin-specific fatty acids (p < 0.05).
In mice fed a mixed HF diet, MPL can limit HF-induced body weight gain and modulate gut physiology and the abundance in microbiota of bacteria of metabolic interest. This supports further exploration of how residual unabsorbed lipids reaching the colon can impact HF-induced metabolic disorders.
肥胖与肠道微生物群和肠道屏障改变有关,其主要特征是脂肪增加和代谢性炎症。本研究旨在探讨牛奶极性脂(MPL)对这些代谢结果的影响,MPL 天然含有 25%的神经鞘磷脂。研究人员用含有混合高脂肪(HF)饮食(21%脂肪,主要是玉米油,在饲料中)的雄性 C57Bl/6 小鼠进行试验,通过乳血清浓缩物的全脂提取物分别补充 1.1%或 1.6%的 MPL(HF-MPL1;HF-MPL2),为期 8 周。与 HF 相比,HF-MPL2 组小鼠体重增加较少(p<0.01)。饮食不影响炎症的血浆标志物,但在肝脏中,HF-MPL2 组与 HF-MPL1 组相比,肝脏巨噬细胞标志物 F4/80 的基因表达呈下降趋势(p=0.06)。HF-MPL2 组结肠隐窝深度最大(p<0.05)。在盲肠微生物群中,HF-MPL1 增加了双歧杆菌属动物与 HF 相比(p<0.05)。HF-MPL2 降低了乳酸杆菌属雷氏菌(p<0.05),其与粪便中牛奶神经鞘磷脂特异性脂肪酸的丢失呈负相关(p<0.05)。
在喂食混合 HF 饮食的小鼠中,MPL 可以限制 HF 引起的体重增加,并调节肠道生理学和微生物群中具有代谢意义的细菌丰度。这支持了进一步探索未被吸收的残留脂质如何影响 HF 引起的代谢紊乱。