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食用色素油的膳食摄入改变了脂肪量过多小鼠的肝脏代谢组学特征。

Dietary Intake of Chromista Oil Alters Hepatic Metabolomic Profile of Mice With Excess Fat Mass.

作者信息

Rust Bret M, Nielsen Forrest H, Yan Lin

机构信息

U.S. Department of Agriculture, Agricultural Research Service, Grand Forks Human Nutrition Research Center, Grand Forks, ND, USA.

出版信息

Nutr Metab Insights. 2024 Nov 19;17:11786388241297143. doi: 10.1177/11786388241297143. eCollection 2024.

Abstract

Increasing dietary intake of fish oil is frequently recommended for decreasing the risk for cardiovascular diseases and improving metabolic health. We hypothesised that dietary intake of chromista oil (a marine food product and a rich source of long-chain n-3 polyunsaturated fatty acids) ameliorates metabolic impairments in mice with established excess adiposity. Three-to 4-week-old mice (male) were fed a control (n = 12) or a high-fat diet (HFD, n = 24) for 12 weeks to establish body fat mass. Then, mice on the HFD were assigned to 2 groups (n = 12 each) with 1 continuing being fed the HFD and the other fed the HFD with chromista oil for an additional 12 weeks. Intake of chromista oil did not affect body weight and body adiposity of the mice fed the HFD; mice fed the HFD had significantly more body weight and fat mass than control mice. The flattened daily oscillations of respiratory exchange ratio induced by the HFD were not changed by chromista oil intake. Intake of chromista oil significantly increased plasma concentration of insulin, the calculated value of HOMA-IR, and plasma concentration of adiponectin in the mice fed the HFD. However, blood glucose was unaffected by chromista oil. Transcription of genes encoding circadian rhythm and fatty acid metabolism of the 2 HFD-fed groups were similar. Untargeted metabolomic analysis showed that intake of chromista oil altered the hepatic metabolomic profile with substantial alterations in amino acid metabolism. Findings from this study indicate that dietary intake of chromista oil does not improve glucose homeostasis or alter the diminished metabolic flexibility in mice with excess adiposity induced by the HFD. argeted metabolomic analysis is warranted to investigate the effects of dietary chromista oil, as a source of n-3 poly unsaturated fatty acids, on metabolism in models of obesity.

摘要

人们经常建议增加鱼油的饮食摄入量,以降低心血管疾病风险并改善代谢健康。我们假设,食用色藻油(一种海洋食品,富含长链n-3多不饱和脂肪酸)可改善已出现肥胖的小鼠的代谢障碍。将3至4周龄的雄性小鼠分为两组,一组喂食对照饮食(n = 12),另一组喂食高脂饮食(HFD,n = 24),持续12周以建立体脂肪量。然后,将高脂饮食组的小鼠再分为两组(每组n = 12),一组继续喂食高脂饮食,另一组在高脂饮食的基础上添加色藻油再喂食12周。色藻油的摄入并未影响高脂饮食喂养小鼠的体重和体脂;喂食高脂饮食的小鼠的体重和脂肪量显著高于对照小鼠。高脂饮食引起的呼吸交换率每日波动变平缓的情况并未因色藻油的摄入而改变。色藻油的摄入显著提高了高脂饮食喂养小鼠的血浆胰岛素浓度、HOMA-IR计算值和脂联素血浆浓度。然而,血糖不受色藻油影响。两组高脂饮食喂养小鼠中编码昼夜节律和脂肪酸代谢的基因转录情况相似。非靶向代谢组学分析表明,色藻油的摄入改变了肝脏代谢组学特征,氨基酸代谢发生了显著变化。本研究结果表明,食用色藻油并不能改善葡萄糖稳态,也不能改变高脂饮食诱导的肥胖小鼠代谢灵活性降低的情况。有必要进行靶向代谢组学分析,以研究作为n-3多不饱和脂肪酸来源的食用色藻油对肥胖模型中代谢的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dac/11577470/275697cd5521/10.1177_11786388241297143-fig1.jpg

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