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高脂饮食揭示 C57BL/6J 肥胖小鼠粪便和肝脏代谢的性别特异性改变。

High fat diet reveals sex-specific fecal and liver metabolic alterations in C57BL/6J obese mice.

机构信息

Department of Chemistry and Chemical Engineering, Florida Institute of Technology, Melbourne, FL, 32901, USA.

Department of Biology, College of Science and Technology, North Carolina Agricultural and Technical State University, Greensboro, NC, 27411, USA.

出版信息

Metabolomics. 2023 Nov 24;19(12):97. doi: 10.1007/s11306-023-02059-x.

Abstract

Obesity is a major health concern that poses significant risks for many other diseases, including diabetes, cardiovascular disease, and cancer. Prevalence of these diseases varies by biological sex. This study utilizes a mouse (C57BL/6J) model of obesity to analyze liver and fecal metabolic profiles at various time points of dietary exposure: 5, 9, and 12 months in control or high fat diet (HFD)-exposed mice. Our study discovered that the female HFD group has a more discernable perturbation and set of significant changes in metabolic profiles than the male HFD group. In the female mice, HFD fecal metabolites including pyruvate, aspartate, and glutamate were lower than control diet-exposed mice after both 9th and 12th month exposure time points, while lactate and alanine were significantly downregulated only at the 12th month. Perturbations of liver metabolic profiles were observed in both male and female HFD groups, compared to controls at the 12th month. Overall, the female HFD group showed higher lactate and glutathione levels compared to controls, while the male HFD group showed higher levels of glutamine and taurine compared to controls. These metabolite-based findings in both fecal and liver samples for a diet-induced effect of obesity may help guide future pioneering discoveries relating to the analysis and prevention of obesity in people, especially for females.

摘要

肥胖是一个主要的健康问题,会对许多其他疾病(包括糖尿病、心血管疾病和癌症)构成重大风险。这些疾病的患病率因生物性别而异。本研究利用肥胖的小鼠(C57BL/6J)模型,在不同的饮食暴露时间点(对照组或高脂肪饮食(HFD)暴露的 5、9 和 12 个月)分析肝脏和粪便的代谢谱。我们的研究发现,与雄性 HFD 组相比,雌性 HFD 组的代谢谱更明显失调,且有更多显著变化。在雌性小鼠中,HFD 粪便代谢物(如丙酮酸、天冬氨酸和谷氨酸)在 9 个月和 12 个月暴露时间点均低于对照组,而乳酸和丙氨酸仅在 12 个月时显著下调。与对照组相比,雄性和雌性 HFD 组在 12 个月时肝脏代谢谱均发生了紊乱。总体而言,与对照组相比,雌性 HFD 组的乳酸和谷胱甘肽水平较高,而雄性 HFD 组的谷氨酰胺和牛磺酸水平较高。这些基于粪便和肝脏样本的代谢物发现可能有助于指导未来对肥胖人群的分析和预防进行开创性的研究,特别是对女性。

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