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二十碳五烯酸在高脂肪/高蔗糖饮食诱导肥胖中的抗肥胖作用:肝内脂肪生成的重要性。

Antiobesity effect of eicosapentaenoic acid in high-fat/high-sucrose diet-induced obesity: importance of hepatic lipogenesis.

机构信息

Development Research, Pharmaceutical Research Center, Mochida Pharmaceutical, Shizuoka, Japan.

出版信息

Diabetes. 2010 Oct;59(10):2495-504. doi: 10.2337/db09-1554. Epub 2010 Aug 3.

Abstract

OBJECTIVE

Given the pleiotropic effect of eicosapentaenoic acid (EPA), it is interesting to know whether EPA is capable of improving obesity. Here we examined the anti-obesity effect of EPA in mice with two distinct models of obesity.

RESEARCH DESIGN AND METHODS

Male C57BL/6J mice were fed a high-fat/high-sucrose diet (25.0% [w/w] fat, 32.5% [w/w] sucrose) (HF/HS group) or a high-fat diet (38.1% [w/w] fat, 8.5% [w/w] sucrose) (HF group) for 4-20 weeks. A total of 5% EPA was administered by partially substituting EPA for fat in the HF/HS + EPA and HF + EPA groups.

RESULTS

Both the HF/HS and HF groups similarly developed obesity. EPA treatment strongly suppresses body weight gain and obesity-related hyperglycemia and hyperinsulinemia in HF/HS-fed mice (HF/HS + EPA group), where hepatic triglyceride content and lipogenic enzymes are increased. There is no appreciable effect of EPA on body weight in HF-fed mice (HF + EPA group) without enhanced expression of hepatic lipogenic enzymes. Moreover, EPA is capable of reducing hepatic triglyceride secretion and changing VLDL fatty acid composition in the HF/HS group. By indirect calorimetry analysis, we also found that EPA is capable of increasing energy consumption in the HF/HS + EPA group.

CONCLUSIONS

This study is the first demonstration that the anti-obesity effect of EPA in HF/HS-induced obesity is associated with the suppression of hepatic lipogenesis and steatosis. Because the metabolic syndrome is often associated with hepatic lipogenesis and steatosis, the data suggest that EPA is suited for treatment of the metabolic syndrome.

摘要

目的

鉴于二十碳五烯酸 (EPA) 的多效性,了解 EPA 是否能够改善肥胖症是很有趣的。在这里,我们研究了 EPA 在两种不同肥胖模型的小鼠中的抗肥胖作用。

研究设计和方法

雄性 C57BL/6J 小鼠喂食高脂肪/高蔗糖饮食(25.0%[w/w]脂肪,32.5%[w/w]蔗糖)(HF/HS 组)或高脂肪饮食(38.1%[w/w]脂肪,8.5%[w/w]蔗糖)(HF 组)4-20 周。HF/HS + EPA 和 HF + EPA 组通过部分用 EPA 替代脂肪中的脂肪来给予 5%的 EPA。

结果

HF/HS 和 HF 组均相似地发展为肥胖症。EPA 治疗强烈抑制 HF/HS 喂养小鼠的体重增加和肥胖相关的高血糖和高胰岛素血症(HF/HS + EPA 组),其中肝甘油三酯含量和脂肪生成酶增加。在没有增强肝脂肪生成酶表达的情况下,EPA 对 HF 喂养小鼠(HF + EPA 组)的体重没有明显影响。此外,EPA 能够减少 HF/HS 组的肝甘油三酯分泌并改变 VLDL 脂肪酸组成。通过间接热量计分析,我们还发现 EPA 能够增加 HF/HS + EPA 组的能量消耗。

结论

本研究首次证明,EPA 在 HF/HS 诱导的肥胖症中的抗肥胖作用与抑制肝脂肪生成和脂肪变性有关。由于代谢综合征常与肝脂肪生成和脂肪变性有关,这些数据表明 EPA 适合治疗代谢综合征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/132d/3279525/5d4092afe04d/zdb0101063130001.jpg

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