蛋白质比例更高的极低碳水化合物饮食可改善饮食诱发非酒精性脂肪肝大鼠的脂质代谢和炎症反应

IF 4.8 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
I-Ting Wu , Wan-Ju Yeh , Wen-Chih Huang , Hsin-Yi Yang
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引用次数: 0

摘要

非酒精性脂肪肝(NAFLD)通常与肥胖有关,主要通过改变生活方式来治疗。超低碳水化合物饮食(VLCD)有助于快速减肥,但极端饮食模式对非酒精性脂肪肝患者的脂质代谢和炎症反应可能产生的影响仍有待商榷。此外,VLCD 的蛋白质含量可能会影响其减肥效果、脂肪变性和炎症反应。因此,我们研究了不同蛋白质含量的 VLCD 对非酒精性脂肪肝大鼠的影响以及这些影响的机制。经过 16 周的诱导期后,大鼠在接下来的 8 周实验期间接受等热量正常饮食(NC 组)或高蛋白含量或低蛋白含量的 VLCD(NVLH 组与 NVLL 组,能量比:蛋白质/碳水化合物/脂质 = 20/1/79 与 6/1/93)。我们注意到,NVLH 组和 NVLL 组的体重都有所下降;不过,NVLH 组的酮病有所改善。NVLL 组可能通过增加极低密度脂蛋白受体(VLDLR)的表达和提高肝脏氧化应激,进而激活 Nrf2 的表达,并通过 TLR4/TRIF/NLRP3 和 TLR4/MyD88/NF-κB途径引发炎症,从而导致肝脏脂质积累。NVLH可部分防止VLDLR和TLR4-炎症体通路的变化。VLCD 还降低了肠道微生物群的多样性并改变了其组成。总之,虽然食用低蛋白VLCD会降低体重,但也可能导致代谢紊乱和微生物群组成的改变;然而,高蛋白VLCD可部分缓解这些限制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Very low-carbohydrate diet with higher protein ratio improves lipid metabolism and inflammation in rats with diet-induced nonalcoholic fatty liver disease

Very low-carbohydrate diet with higher protein ratio improves lipid metabolism and inflammation in rats with diet-induced nonalcoholic fatty liver disease

Non-alcoholic fatty liver disease (NAFLD) is commonly associated with obesity, and it is mainly treated through lifestyle modifications. The very low-carbohydrate diet (VLCD) can help lose weight rapidly but the possible effects of extreme dietary patterns on lipid metabolism and inflammatory responses in individuals with NAFLD remain debatable. Moreover, VLCD protein content may affect its effectiveness in weight loss, steatosis, and inflammatory responses. Therefore, we investigated the effects of VLCDs with different protein contents in NAFLD rats and the mechanisms underlying these effects. After a 16-week inducing period, the rats received an isocaloric normal diet (NC group) or a VLCD with high or low protein content (NVLH vs. NVLL group, energy ratio:protein/carbohydrate/lipid=20/1/79 vs. 6/1/93) for the next 8 weeks experimental period. We noted that the body weight decreased in both the NVLH and NVLL groups; nevertheless, the NVLH group demonstrated improvements in ketosis. The NVLL group led to hepatic lipid accumulation, possibly by increasing very-low-density lipoprotein receptor (VLDLR) expression and elevating liver oxidative stress, subsequently activating the expression of Nrf2, and inflammation through the TLR4/TRIF/NLRP3 and TLR4/MyD88/NF-κB pathway. The NVLH was noted to prevent the changes in VLDLR and the TLR4-inflammasome pathway partially. The VLCD also reduced the diversity of gut microbiota and changed their composition. In conclusion, although low-protein VLCD consumption reduces BW, it may also lead to metabolic disorders and changes in microbiota composition; nevertheless, a VLCD with high protein content may partially alleviate these limitations.

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来源期刊
Journal of Nutritional Biochemistry
Journal of Nutritional Biochemistry 医学-生化与分子生物学
CiteScore
9.50
自引率
3.60%
发文量
237
审稿时长
68 days
期刊介绍: Devoted to advancements in nutritional sciences, The Journal of Nutritional Biochemistry presents experimental nutrition research as it relates to: biochemistry, molecular biology, toxicology, or physiology. Rigorous reviews by an international editorial board of distinguished scientists ensure publication of the most current and key research being conducted in nutrition at the cellular, animal and human level. In addition to its monthly features of critical reviews and research articles, The Journal of Nutritional Biochemistry also periodically publishes emerging issues, experimental methods, and other types of articles.
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