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饮食能量摄入和异常隐窝病灶的存在与 C57BL/6N 小鼠结肠中磷脂、嘌呤和牛磺酸代谢物的丰度相关。

Dietary Energy Intake and Presence of Aberrant Crypt Foci Are Associated with Phospholipid, Purine, and Taurine Metabolite Abundances in C57BL/6N Mouse Colon.

机构信息

OSU Interdisciplinary Nutrition PhD Program (OSUN), Department of Human Sciences, The Ohio State University, 1787 Neil Ave, Columbus, OH, 43210, United States.

Division of Preclinical Innovation Informatics Core, National Center for Advancing Translational Sciences, 9800 Medical Center Drive, Rockville, MD, 20850, USA.

出版信息

Mol Nutr Food Res. 2022 Oct;66(20):e2200180. doi: 10.1002/mnfr.202200180.

Abstract

SCOPE

Colon metabolomes associated with high-fat (H) versus energy-restricted (E) diets in early colorectal cancer (CRC) models have never been directly compared. The objectives of this study are to elucidate metabolites associated with diet, aberrant crypt foci (ACF), and diet:ACF interaction, using a lifetime murine model.

METHODS AND RESULTS

Three-week-old mice consumed control (C), E, or H initiation diets for 18 weeks. ACF formation is initiated weeks 16-21 with azoxymethane injections, followed by progression diet crossover (to C, E, or H) through week 60. Colon extracts are analyzed using ultra-high-performance liquid chromatography-high resolution mass spectrometry (UHPLC-HRMS). Metabolites associated with diet, ACF, or diet:ACF are determined using regression models (FDR-adjusted p-value <0.05). No metabolites are significantly associated with initiation diets, but concentrations of acylcarnitines and phospholipids are associated with C, E, and H progression diets. Purines, taurine, and phospholipids are associated with ACF presence. No significant associations between metabolites and diet:ACF interaction are observed.

CONCLUSIONS

These results suggest that recent, rather than early-life, diet is more closely associated with the colon metabolome, particularly lipid metabolism. Results from this study also provide candidate biomarkers of early CRC development and provide support for the importance of early diet on influencing pre-CRC risk.

摘要

范围

高脂肪(H)与能量限制(E)饮食与早期结直肠癌(CRC)模型中结肠代谢组的关联从未被直接比较过。本研究的目的是使用终生小鼠模型阐明与饮食、异常隐窝病灶(ACF)以及饮食:ACF 相互作用相关的代谢物。

方法和结果

3 周龄的小鼠接受对照(C)、E 或 H 起始饮食 18 周。ACF 形成始于第 16-21 周,用氧化偶氮甲烷注射启动,然后在第 60 周前进行进展饮食交叉(C、E 或 H)。使用超高效液相色谱-高分辨率质谱(UHPLC-HRMS)分析结肠提取物。使用回归模型(FDR 调整后的 p 值 <0.05)确定与饮食、ACF 或饮食:ACF 相关的代谢物。没有代谢物与起始饮食显著相关,但酰基肉碱和磷脂的浓度与 C、E 和 H 进展饮食相关。嘌呤、牛磺酸和磷脂与 ACF 的存在相关。未观察到代谢物与饮食:ACF 相互作用之间存在显著关联。

结论

这些结果表明,近期而非早期生活的饮食与结肠代谢组更为密切相关,特别是脂质代谢。本研究的结果还提供了早期 CRC 发展的候选生物标志物,并支持早期饮食对影响前 CRC 风险的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bea/9787839/28364b64fd8f/MNFR-66-2200180-g001.jpg

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