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补充L-蛋氨酸可通过调节大鼠的脂质代谢、纤维化和炎症来减轻高脂果糖饮食诱导的非酒精性脂肪性肝炎。

L-Methionine supplementation attenuates high-fat fructose diet-induced non-alcoholic steatohepatitis by modulating lipid metabolism, fibrosis, and inflammation in rats.

作者信息

Navik Umashanker, Sheth Vaibhav G, Sharma Nisha, Tikoo Kulbhushan

机构信息

Laboratory of Epigenetics and Diseases, Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research, Sector-67, S.A.S. Nagar, Punjab-160062, India.

Department of Pharmacology, Central University of Punjab, Ghudda, Bathinda, Punjab-151401, India.

出版信息

Food Funct. 2022 May 10;13(9):4941-4953. doi: 10.1039/d1fo03403k.

Abstract

Recently, the protective effects of a methionine-rich diet on hepatic oxidative stress and fibrosis have been suggested but not adequately studied. We, therefore, hypothesized that L-methionine supplementation would ameliorate the progression of hepatic injury in a diet-induced non-alcoholic steatohepatitis (NASH) model and aimed to investigate the underlying mechanism. NASH was developed in male Sprague Dawley rats by feeding them with a high-fat-fructose diet (HFFrD) for 10 weeks. The results demonstrated that L-methionine supplementation to NASH rats for 16 weeks improved the glycemic, lipid, and liver function profiles in NASH rats. Histological analysis of liver tissue revealed a remarkable improvement in the three classical lesions of NASH: steatosis, inflammation, and ballooning. Besides, L-methionine supplementation ameliorated the HFFrD-induced enhanced lipogenesis and lipid peroxidation. An anti-inflammatory effect of L-methionine was also observed through the inhibition of the release of proinflammatory cytokines. Furthermore, the hepatic SIRT1/AMPK signaling pathway was associated with the beneficial effects of L-methionine. This study demonstrates that L-methionine supplementation in HFFrD-fed rats improves their liver pathology regulation of lipogenesis, inflammation, and the SIRT1/AMPK pathway, thus encouraging its clinical evaluation for the treatment of NASH.

摘要

最近,有人提出富含蛋氨酸的饮食对肝脏氧化应激和纤维化具有保护作用,但尚未得到充分研究。因此,我们假设补充L-蛋氨酸可以改善饮食诱导的非酒精性脂肪性肝炎(NASH)模型中肝损伤的进展,并旨在研究其潜在机制。通过给雄性Sprague Dawley大鼠喂食高脂果糖饮食(HFFrD)10周来建立NASH模型。结果表明,给NASH大鼠补充L-蛋氨酸16周可改善其血糖、血脂和肝功能指标。肝组织的组织学分析显示NASH的三个典型病变(脂肪变性、炎症和气球样变)有显著改善。此外,补充L-蛋氨酸改善了HFFrD诱导的脂肪生成增加和脂质过氧化。通过抑制促炎细胞因子的释放,还观察到了L-蛋氨酸的抗炎作用。此外,肝脏SIRT1/AMPK信号通路与L-蛋氨酸的有益作用有关。本研究表明,在喂食HFFrD的大鼠中补充L-蛋氨酸可改善其肝脏病理、脂肪生成调节、炎症以及SIRT1/AMPK通路,从而鼓励对其进行治疗NASH的临床评估。

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