The Origins, Evolution, and Future of Dietary Methionine Restriction.

IF 12.6 2区 医学 Q1 NUTRITION & DIETETICS
Annual review of nutrition Pub Date : 2022-08-22 Epub Date: 2022-05-19 DOI:10.1146/annurev-nutr-062320-111849
Han Fang, Kirsten P Stone, Desiree Wanders, Laura A Forney, Thomas W Gettys
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引用次数: 0

Abstract

The original description of dietary methionine restriction (MR) used semipurified diets to limit methionine intake to 20% of normal levels, and this reduction in dietary methionine increased longevity by ∼30% in rats. The MR diet also produces paradoxical increases in energy intake and expenditure and limits fat deposition while reducing tissue and circulating lipids and enhancing overall insulin sensitivity. In the years following the original 1993 report, a comprehensive effort has been made to understand the nutrient sensing and signaling systems linking reduced dietary methionine to the behavioral, physiological, biochemical, and transcriptional components of the response. Recent work has shown that transcriptional activation of hepatic fibroblast growth factor 21 (FGF21) is a key event linking the MR diet to many but not all components of its metabolic phenotype. These findings raise the interesting possibility of developing therapeutic, MR-based diets that produce the beneficial effects of FGF21 by nutritionally modulating its transcription and release.

膳食蛋氨酸限制的起源、演变和未来。
最初对蛋氨酸饮食限制(MR)的描述是使用半净化饮食将蛋氨酸摄入量限制在正常水平的 20%,这种饮食蛋氨酸的减少使大鼠的寿命延长了 30%。MR 饮食还能增加能量摄入和消耗,限制脂肪沉积,同时降低组织和循环血脂,提高整体胰岛素敏感性。在 1993 年最初的报告发表后的几年里,人们一直在努力全面了解将膳食蛋氨酸减少与行为、生理、生化和转录反应成分联系起来的营养传感和信号系统。最近的研究表明,肝脏成纤维细胞生长因子 21(FGF21)的转录激活是将 MR 膳食与代谢表型的许多成分(而非所有成分)联系起来的关键事件。这些发现为开发基于 MR 的治疗性饮食提供了有趣的可能性,这种饮食通过营养调节 FGF21 的转录和释放来产生有益的效果。
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来源期刊
Annual review of nutrition
Annual review of nutrition 医学-营养学
CiteScore
15.80
自引率
0.00%
发文量
19
期刊介绍: Annual Review of Nutrition Publication History:In publication since 1981 Scope:Covers significant developments in the field of nutrition Topics Covered Include: Energy metabolism; Carbohydrates; Lipids; Proteins and amino acids; Vitamins; Minerals; Nutrient transport and function; Metabolic regulation; Nutritional genomics; Molecular and cell biology; Clinical nutrition; Comparative nutrition; Nutritional anthropology; Nutritional toxicology; Nutritional microbiology; Epidemiology; Public health nutrition
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