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Dietary methionine restriction reduces hepatic steatosis and oxidative stress in high-fat-fed mice by promoting H2S production

机译:通过促进H2S生产,膳食蛋氨酸限制可降低高脂肪喂养小鼠的肝脏脂肪变性和氧化应激

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摘要

Methionine is an essential amino acid that plays important roles in mammalian metabolism. Interestingly, previous studies have consistently shown that a methionine-restricted diet (MRD) reduces hepatic lipid levels, reactive oxygen species production, and oxidative stress damage. However, the mechanisms responsible for these beneficial effects are unknown. Therefore, our study was aimed at investigating the hepatic systemic metabolic responses to MRD in high-fat-diet (HFD) mice and to clarify the possible mechanisms of such responses. C57BL/6J mice were fed a control diet (0.86% methionine + 4% fat), HFD (0.86% methionine + 20% fat), or MRD (0.17% methionine + 20% fat) for 22 consecutive weeks, and euthanized at week 11 or week 22. Our results showed that HFD inhibited hepatic energy expenditure, induced steatosis and oxidative stress, and decreased hydrogen sulfide (H2S) production in the mouse liver. MRD reduced the body weight, liver fat percentage, and plasma and hepatic lipid profiles. Moreover, MRD decreased lipid synthesis, increased energy metabolism (e.g. lipid catabolism and fatty acid oxidation, glycolysis and tricarboxylic acid cycle metabolism, and amino acid catabolism), enhanced the activity of antioxidant enzymes, and reduced the levels of oxidative damage products and purine metabolism in the liver. Furthermore, MRD up-regulated the hepatic gene and protein expression of cystathionine-gamma-lyase (CSE), elevated the hepatic CSE activity, and promoted hepatic H2S production. These findings suggest that MRD can ameliorate the hepatic metabolic disorders induced by HFD and especially reduce hepatic steatosis and oxidative stress likely through increasing hepatic H2S production.
机译:甲硫氨酸是一种在哺乳动物代谢中起重要作用的必需氨基酸。有趣的是,先前的研究一直表明甲硫氨酸限制饮食(MRD)可降低肝脂质水平,反应性氧物质生产和氧化应激损伤。然而,负责这些有益效果的机制是未知的。因此,我们的研究旨在调查高脂饮食(HFD)小鼠的MRD的肝脏系统性代谢反应,并阐明这种反应的可能机制。将C57BL / 6J小鼠在连续22周内加入控制饮食(0.86%甲硫氨酸+ 4%脂肪),HFD(0.86%甲硫氨酸+ 20%脂肪),或MRD(0.17%甲硫氨酸+ 20%脂肪),并在一周内安乐死11或第22周。我们的结果表明,HFD抑制了肝脏能量消耗,诱导的脂肪变性和氧化应激,并降低小鼠肝脏中的硫化氢(H2S)产生。 MRD减少了体重,肝脂肪百分比和血浆和肝脂肪曲线。此外,MRD降低了脂质合成,增加能量代谢(例如脂质分解代谢和脂肪酸氧化,糖酵解和三羧酸循环代谢,以及氨基酸分解代谢),增强了抗氧化酶的活性,降低了氧化损伤产物和嘌呤代谢的活性。在肝脏。此外,MRD上调肝脏基因和胱硫脲-γ-裂解酶(CSE)的蛋白表达,升高了肝癌活性,并促进了肝脏H2S的产生。这些发现表明,MRD可以改善HFD诱导的肝脏代谢紊乱,特别是通过增加肝脏H2S生产可能降低肝脏脂肪变性和氧化应激。

著录项

  • 来源
    《Food & Function》 |2019年第1期|共17页
  • 作者单位

    Jiangnan Univ State Key Lab Food Sci &

    Technol Wuxi 214122 Jiangsu Peoples R China;

    Jiangnan Univ Sch Food Sci &

    Technol Ctr Food Nutr &

    Funct Food Engn Wuxi 214122 Jiangsu Peoples R China;

    Jiangnan Univ State Key Lab Food Sci &

    Technol Wuxi 214122 Jiangsu Peoples R China;

    Jiangnan Univ Sch Food Sci &

    Technol Ctr Food Nutr &

    Funct Food Engn Wuxi 214122 Jiangsu Peoples R China;

    Jiangnan Univ Sch Food Sci &

    Technol Ctr Food Nutr &

    Funct Food Engn Wuxi 214122 Jiangsu Peoples R China;

    Jiangnan Univ State Key Lab Food Sci &

    Technol Wuxi 214122 Jiangsu Peoples R China;

    Jiangnan Univ State Key Lab Food Sci &

    Technol Wuxi 214122 Jiangsu Peoples R China;

    Jiangnan Univ State Key Lab Food Sci &

    Technol Wuxi 214122 Jiangsu Peoples R China;

    Jiangnan Univ State Key Lab Food Sci &

    Technol Wuxi 214122 Jiangsu Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 食品工业;
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