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裂殖壶菌属的微藻油可预防高脂饮食诱导的小鼠腹部脂肪堆积。

Microalgal Oil from Schizochytrium sp. Prevents HFD-Induced Abdominal Fat Accumulation in Mice.

作者信息

Yu Jinhui, Ma Yong, Sun Jie, Ran Liyuan, Li Youwei, Wang Ning, Yu Tao, Gao Wenting, Jia Wenbin, Jiang Rujiao, Guo Meihua, Bi Yuping, Wu Yingjie

机构信息

a Institute for Genome Engineered Animal Models of Human Diseases , Dalian Medical University , Dalian , Liaoning , China.

b College of Integrative Medicine , Dalian Medical University , Dalian , Liaoning , China.

出版信息

J Am Coll Nutr. 2017 Jul;36(5):347-356. doi: 10.1080/07315724.2017.1302366. Epub 2017 May 26.

Abstract

OBJECTIVE

Dietary n-3 polyunsaturated fatty acids (PUFAs), especially eicosapentaenoic acids (EPA) and docosahexaenoic acid (DHA), are proved to be effective in obesity reduction. Microalgal oil (MO) is an important alternative source of n-3 PUFAs that effectively alleviates obesity. The aim of the present study was to explore the anti-obesity effects of microalgal oil from Schizochytrium sp. (SMO) and to compare the effects of 2 SMOs (SMO1 and SMO2) with different levels of purity of n-3 PUFAs on high fat diet (HFD)-induced obesity in male C57BL/6J mice.

METHODS

Mice were randomly divided into 5 groups: (1) regular chow (RC); (2) HFD; (3) HFD + fish oil (FO); (4) HFD + SMO1; and (5) HFD + SMO2. Body weight and food intake were weekly monitored. After 16 weeks of treatment, a glucose tolerance test (GTT) and an insulin tolerance test (ITT) were performed. Serum lipid profile, morphological changes in the liver and epididymal white adipose tissue (eWAT), and the mRNA expression of lipid metabolism-related genes were also examined.

RESULTS

SMO treatment significantly decreased HFD-induced abdominal fat accumulation, lowered the levels of triglycerides, cholesterol, and low-density lipoprotein, as did the positive control treated with FO. Morphological examination revealed a remarkable reduction in lipid droplet formation in the liver tissue and the particle size of eWAT. An alleviation of inflammation infiltration in eWAT caused by a high-fat diet was also observed. Real-time reverse transcription-polymerase chain reaction analysis examination confirmed that microalgal oil inhibited the gene expression of fatty acid synthase, sterol responsive element-binding protein-1c, and acetyl-CoA carboxylase but promoted that of hormone-sensitive lipase and lipoprotein lipase, carnitine palmitoyltransferase-1, and uncoupling proteins in the liver and eWAT. Moreover, similar anti-obesity effects were obtained with the same dosage but different purity of n-3 PUFAs.

CONCLUSIONS

As an alternative n-3 PUFAs resource, dietary intake of SMO might be beneficial to prevent HFD-induced abdominal fat accumulation.

摘要

目的

膳食中的n-3多不饱和脂肪酸(PUFAs),尤其是二十碳五烯酸(EPA)和二十二碳六烯酸(DHA),已被证明对减轻肥胖有效。微藻油(MO)是n-3多不饱和脂肪酸的重要替代来源,可有效缓解肥胖。本研究的目的是探讨裂殖壶菌属微藻油(SMO)的抗肥胖作用,并比较两种不同n-3多不饱和脂肪酸纯度水平的SMO(SMO1和SMO2)对雄性C57BL/6J小鼠高脂饮食(HFD)诱导肥胖的影响。

方法

将小鼠随机分为5组:(1)正常饲料(RC)组;(2)高脂饮食(HFD)组;(3)高脂饮食+鱼油(FO)组;(4)高脂饮食+SMO1组;(5)高脂饮食+SMO2组。每周监测体重和食物摄入量。治疗16周后,进行葡萄糖耐量试验(GTT)和胰岛素耐量试验(ITT)。还检测了血清脂质谱、肝脏和附睾白色脂肪组织(eWAT)的形态变化以及脂质代谢相关基因的mRNA表达。

结果

SMO治疗显著降低了HFD诱导的腹部脂肪堆积,降低了甘油三酯、胆固醇和低密度脂蛋白水平,与用FO治疗的阳性对照组效果相同。形态学检查显示肝组织中脂滴形成和eWAT颗粒大小显著减少。还观察到高脂饮食引起的eWAT炎症浸润减轻。实时逆转录-聚合酶链反应分析证实,微藻油抑制了脂肪酸合酶、固醇调节元件结合蛋白-1c和乙酰辅酶A羧化酶的基因表达,但促进了肝脏和eWAT中激素敏感性脂肪酶、脂蛋白脂肪酶、肉碱棕榈酰转移酶-1和解偶联蛋白的基因表达。此外,相同剂量但不同纯度的n-3多不饱和脂肪酸获得了相似的抗肥胖效果。

结论

作为n-3多不饱和脂肪酸的替代资源,膳食摄入SMO可能有助于预防HFD诱导的腹部脂肪堆积。

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