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生命早期补充花生四烯酸/二十二碳六烯酸的饮食可降低载脂蛋白 E*3Leiden 小鼠生命后期的体重增加、血浆脂质和肥胖程度。

Arachidonic acid/docosahexaenoic acid-supplemented diet in early life reduces body weight gain, plasma lipids, and adiposity in later life in ApoE*3Leiden mice.

机构信息

TNO Metabolic Health Research, Leiden, The Netherlands.

出版信息

Mol Nutr Food Res. 2012 Jul;56(7):1081-9. doi: 10.1002/mnfr.201100762. Epub 2012 May 18.

Abstract

SCOPE

This study addresses whether early life arachidonic acid (ARA)/docosahexaenoic acid (DHA) supplementation or eicosapentaenoic acid (EPA)/DHA (Omacor) supplementation affects body weight gain, lipid metabolism, and adipose tissue quantity and quality in later life in ApoE*3Leiden-transgenic mice, a humanized model for hyperlipidemia and mild obesity.

METHODS AND RESULTS

Four-week-old male ApoE*3Leiden mice were fed chow diet with or without a mixture of ARA (0.129 wt%) and DHA (0.088 wt%) or Omacor (0.30 wt% EPA, 0.25 wt% DHA). At age 12 weeks, mice were fed high-fat/high-carbohydrate (HFHC) diet without above supplements until age 20 weeks. Control mice received chow diet throughout the study. Mice receiving ARA/DHA gained less body weight compared to control and this effect was sustained when fed HFHC. Omacor had no significant effect on body weight gain. Plasma cholesterol and triglycerides were significantly lowered by both supplementations. At 20 weeks, epididymal fat mass was less in ARA/DHA-supplemented mice, while Omacor had no significant effect on fat mass. Both ARA/DHA and Omacor reduced inguinal adipocyte cell size; only ARA/DHA significantly reduced epididymal macrophage infiltration.

CONCLUSION

This study shows that early life ARA/DHA, but not Omacor supplementation improves body weight gain later in life. ARA/DHA and to a lesser extent Omacor both improved adipose tissue quality.

摘要

研究范围

本研究旨在探讨在载脂蛋白 E3 莱顿(ApoE3Leiden)转基因小鼠(一种高血脂和轻度肥胖的人源化模型)中,早期补充花生四烯酸(ARA)/二十二碳六烯酸(DHA)或二十碳五烯酸(EPA)/二十二碳六烯酸(DHA)(Omacor)是否会影响其生命后期的体重增长、脂质代谢以及脂肪组织的数量和质量。

方法与结果

4 周龄雄性 ApoE*3Leiden 小鼠食用含或不含 ARA(0.129wt%)和 DHA(0.088wt%)混合物或 Omacor(0.30wt% EPA、0.25wt% DHA)的标准饮食。12 周龄时,小鼠开始喂食高脂肪/高碳水化合物(HFHC)饮食,不再添加上述补充剂,直至 20 周龄。对照组小鼠在整个研究过程中均喂食标准饮食。与对照组相比,补充 ARA/DHA 的小鼠体重增长较慢,而喂食 HFHC 时这种效果持续存在。Omacor 对体重增长没有显著影响。两种补充剂均显著降低了血浆胆固醇和甘油三酯水平。20 周龄时,补充 ARA/DHA 的小鼠附睾脂肪质量减少,而 Omacor 对脂肪质量没有显著影响。ARA/DHA 和 Omacor 均可减少腹股沟脂肪细胞的大小;只有 ARA/DHA 可显著减少附睾巨噬细胞浸润。

结论

本研究表明,生命早期补充 ARA/DHA 而非 Omacor 可改善生命后期的体重增长。ARA/DHA 和 Omacor 均可改善脂肪组织质量,且 ARA/DHA 的作用更为明显。

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