长期摄入乳脂不会显著增加正常和高脂饮食小鼠的血脂负荷。

IF 23.7 Q1 MICROBIOLOGY
iMeta Pub Date : 2024-12-15 DOI:10.1002/imt2.256
Guang-Xu Ren, Liang He, Yong-Xin Liu, Yu-Ke Fei, Xiao-Fan Liu, Qiu-Yi Lu, Xin Chen, Zhi-Da Song, Jia-Qi Wang
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引用次数: 0

摘要

以正常饮食(ND)或高脂饮食(HFD)喂养C57BL/6J小鼠10周后,进行为期7周的乳脂和全脂牛奶干预,以评估它们对宿主血脂水平的长期影响。结果表明,乳脂和全脂牛奶均未显著提高ND-或hfd喂养小鼠的低密度脂蛋白胆固醇(LDL-C)。在ND小鼠中,乳脂和全脂牛奶改善了肠道菌群多样性和扩增子序列变异。关键细菌属如Blautia、Romboutsia和Prevotellaceae_NK3B31_group被鉴定为LDL-C和高密度脂蛋白胆固醇(HDL-C)的双向调节因子。六种独特的代谢物也与LDL-C和HDL-C调节有关。此外,优化的机器学习模型基于肠道微生物群数据准确预测LDL-C (R²= 0.96)和HDL-C (R²= 0.89),其中80%的顶级预测特征是受乳脂和全脂牛奶影响的肠道代谢物。这些发现表明,长期摄入乳脂不会显著增加血脂负担,基于肠道微生物群和代谢物的机器学习算法为早期脂质评估和个性化营养策略提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The long-term intake of milk fat does not significantly increase the blood lipid burden in normal and high-fat diet-fed mice

The long-term intake of milk fat does not significantly increase the blood lipid burden in normal and high-fat diet-fed mice

After 10 weeks of feeding C57BL/6J mice with a normal diet (ND) or a high-fat diet (HFD), a 7-week intervention with milk fat and whole milk was conducted to assess their long-term effects on host blood lipid levels. The results showed that milk fat and whole milk did not significantly elevate low-density lipoprotein cholesterol (LDL-C) in either ND- or HFD-fed mice. In ND mice, milk fat and whole milk improved gut microbiota diversity and Amplicon Sequence Variants. Key bacterial genera, such as Blautia, Romboutsia, and Prevotellaceae_NK3B31_group, were identified as bidirectional regulators of LDL-C and high-density lipoprotein cholesterol (HDL-C). Six unique metabolites were also linked to LDL-C and HDL-C regulation. Furthermore, an optimized machine learning model accurately predicted LDL-C (R² = 0.96) and HDL-C (R² = 0.89) based on gut microbiota data, with 80% of the top predictive features being gut metabolites influenced by milk fat and whole milk. These findings indicate that the long-term intake of milk fat does not significantly increase the blood lipid burden, and machine learning algorithms based on gut microbiota and metabolites offer novel insights for early lipid assessment and personalized nutrition strategies.

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