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鱼油可增加小鼠饮食诱导的产热。

Fish Oil Increases Diet-Induced Thermogenesis in Mice.

机构信息

Department of Nutrition and Metabolism, National Institute of Health and Nutrition, National Institutes of Biomedical Innovation, Health and Nutrition, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8636, Japan.

The Graduate School of Humanities and Sciences, Ochanomizu University, 2-1-1 Otsuka, Bunkyo-ku, Tokyo 112-8610, Japan.

出版信息

Mar Drugs. 2021 May 17;19(5):278. doi: 10.3390/md19050278.

Abstract

Increasing energy expenditure (EE) is beneficial for preventing obesity. Diet-induced thermogenesis (DIT) is one of the components of total EE. Therefore, increasing DIT is effective against obesity. We examined how much fish oil (FO) increased DIT by measuring absolute values of DIT in mice. C57BL/6J male mice were given diets of 30 energy% fat consisting of FO or safflower oil plus butter as control oil (Con). After administration for 9 days, respiration in mice was monitored, and then the data were used to calculate DIT and EE. DIT increased significantly by 1.2-fold in the FO-fed mice compared with the Con-fed mice. Body weight gain was significantly lower in the FO-fed mice. FO increased the levels of uncoupling protein 1 () mRNA and UCP1 protein in brown adipose tissue (BAT) by 1.5- and 1.2-fold, respectively. In subcutaneous white adipose tissue (subWAT), the levels of mRNA and UCP1 protein were increased by 6.3- and 2.7-fold, respectively, by FO administration. FO also significantly increased the expression of markers of browning in subWAT such as fibroblast growth factor 21 and cell death-inducing DNA fragmentation factor α-like effector a. Thus, dietary FO seems to increase DIT in mice via the increased expressions of in BAT and induced browning of subWAT. FO might be a promising dietary fat in the prevention of obesity by upregulation of energy metabolism.

摘要

增加能量消耗(EE)有益于预防肥胖。饮食诱导的产热(DIT)是总 EE 的组成部分之一。因此,增加 DIT 对肥胖症是有效的。我们通过测量小鼠 DIT 的绝对值来研究鱼油(FO)能增加多少 DIT。将 C57BL/6J 雄性小鼠给予 30%能量脂肪的饮食,其中 FO 或红花油加黄油作为对照油(Con)。给药 9 天后,监测小鼠的呼吸,然后使用这些数据计算 DIT 和 EE。与 Con 组相比,FO 组的 DIT 显著增加了 1.2 倍。FO 组的体重增加明显较低。FO 分别使棕色脂肪组织(BAT)中解偶联蛋白 1(UCP1)mRNA 和 UCP1 蛋白的水平增加了 1.5 倍和 1.2 倍。在皮下白色脂肪组织(subWAT)中,FO 给药使 mRNA 和 UCP1 蛋白的水平分别增加了 6.3 倍和 2.7 倍。FO 还显著增加了 subWAT 中褐色标记物的表达,如成纤维细胞生长因子 21 和细胞死亡诱导 DNA 片段化因子α样效应物 a。因此,膳食 FO 似乎通过增加 BAT 中的 表达和诱导 subWAT 的褐色化,增加了小鼠的 DIT。FO 通过上调能量代谢,可能成为预防肥胖的有前途的膳食脂肪。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b5c/8156710/cdc09499c291/marinedrugs-19-00278-g001.jpg

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