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本文引用的文献

1
The effects of graded levels of calorie restriction: XI. Evaluation of the main hypotheses underpinning the life extension effects of CR using the hepatic transcriptome.不同程度热量限制的影响:XI. 使用肝脏转录组评估支持热量限制延长寿命作用的主要假说。
Aging (Albany NY). 2017 Jul 31;9(7):1770-1824. doi: 10.18632/aging.101269.
2
Calorie restriction in rodents: Caveats to consider.啮齿动物的热量限制:需要考虑的注意事项。
Ageing Res Rev. 2017 Oct;39:15-28. doi: 10.1016/j.arr.2017.05.008. Epub 2017 Jun 10.
3
Dietary treatment of fatty liver: High dietary protein content has an antisteatotic and antiobesogenic effect in mice.饮食治疗脂肪肝:高膳食蛋白质含量可在小鼠中产生抗脂肪变性和抗肥胖作用。
Biochim Biophys Acta Mol Basis Dis. 2017 Jul;1863(7):1789-1804. doi: 10.1016/j.bbadis.2017.04.022. Epub 2017 Apr 28.
4
Long-term intake of a high-protein diet increases liver triacylglycerol deposition pathways and hepatic signs of injury in rats.长期摄入高蛋白饮食会增加大鼠肝脏三酰甘油沉积途径及肝脏损伤迹象。
J Nutr Biochem. 2017 Aug;46:39-48. doi: 10.1016/j.jnutbio.2017.04.008. Epub 2017 Apr 19.
5
Caloric restriction improves health and survival of rhesus monkeys.热量限制可改善恒河猴的健康和寿命。
Nat Commun. 2017 Jan 17;8:14063. doi: 10.1038/ncomms14063.
6
Defining the Nutritional and Metabolic Context of FGF21 Using the Geometric Framework.使用几何框架定义 FGF21 的营养和代谢背景。
Cell Metab. 2016 Oct 11;24(4):555-565. doi: 10.1016/j.cmet.2016.09.001. Epub 2016 Sep 29.
7
Cystathionine-Gamma-Lyase Gene Deletion Protects Mice against Inflammation and Liver Sieve Injury following Polymicrobial Sepsis.胱硫醚-γ-裂解酶基因缺失保护小鼠免受多微生物败血症后的炎症和肝筛损伤。
PLoS One. 2016 Aug 12;11(8):e0160521. doi: 10.1371/journal.pone.0160521. eCollection 2016.
8
PPARα Downregulates Hepatic Glutaminase Expression in Mice Fed Diets with Different Protein:Carbohydrate Ratios.在喂食不同蛋白质:碳水化合物比例饮食的小鼠中,过氧化物酶体增殖物激活受体α(PPARα)下调肝脏谷氨酰胺酶的表达。
J Nutr. 2016 Sep;146(9):1634-40. doi: 10.3945/jn.116.232868. Epub 2016 Jul 27.
9
Effects of Sex, Strain, and Energy Intake on Hallmarks of Aging in Mice.性别、品系和能量摄入对小鼠衰老特征的影响。
Cell Metab. 2016 Jun 14;23(6):1093-1112. doi: 10.1016/j.cmet.2016.05.027.
10
Enrichr: a comprehensive gene set enrichment analysis web server 2016 update.Enrichr:一个全面的基因集富集分析网络服务器2016年更新版。
Nucleic Acids Res. 2016 Jul 8;44(W1):W90-7. doi: 10.1093/nar/gkw377. Epub 2016 May 3.

衰老小鼠长期膳食宏量营养素与肝脏基因表达。

Long-term Dietary Macronutrients and Hepatic Gene Expression in Aging Mice.

机构信息

Charles Perkins Centre, University of Sydney, New South Wales, Australia.

Aging and Alzheimers Institute (AAAI), New South Wales, Australia.

出版信息

J Gerontol A Biol Sci Med Sci. 2018 Nov 10;73(12):1618-1625. doi: 10.1093/gerona/gly065.

DOI:10.1093/gerona/gly065
PMID:29688281
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6454416/
Abstract

Nutrition influences both hepatic function and aging, but mechanisms are poorly understood. Here, the effects of lifelong, ad libitum-fed diets varying in macronutrients and energy on hepatic gene expression were studied. Gene expression was measured using Affymetrix mouse arrays in livers of 46 mice aged 15 months fed one of 25 diets varying in protein, carbohydrates, fat, and energy density from 3 weeks of age. Gene expression was almost entirely influenced by protein intake. Carbohydrate and fat intake had few effects on gene expression compared with protein. Pathways and processes associated with protein intake included those involved with mitochondrial function, metabolic signaling (PI3K-Akt, AMPK, mTOR) and metabolism of protein and amino acids. Protein intake had variable effects on genes associated with regulation of longevity and influenced by caloric restriction. Among the genes of interest with expression that were significantly associated with protein intake are Cth, Gls2, Igf1, and Nnmt, which were increased with higher protein intake, and Igf2bp2, Fgf21, Prkab2, and Mtor, which were increased with lower protein intake. Dietary protein has a powerful impact on hepatic gene expression in older mice, with some overlap with genes previously reported to be involved with regulation of longevity or caloric restriction.

摘要

营养既影响肝脏功能,又影响衰老,但其中的机制尚不清楚。在这里,我们研究了终生、自由进食的不同宏量营养素和能量的饮食对肝脏基因表达的影响。在 46 只 15 个月大的老鼠的肝脏中,使用 Affymetrix 小鼠芯片测量了从 3 周龄起就开始食用的 25 种不同饮食的基因表达情况,这些饮食在蛋白质、碳水化合物、脂肪和能量密度方面存在差异。基因表达几乎完全受蛋白质摄入的影响。与蛋白质相比,碳水化合物和脂肪的摄入对基因表达的影响很小。与蛋白质摄入相关的途径和过程包括那些与线粒体功能、代谢信号(PI3K-Akt、AMPK、mTOR)以及蛋白质和氨基酸代谢相关的途径和过程。蛋白质摄入对与长寿调节相关且受热量限制影响的基因有可变的影响。在与蛋白质摄入显著相关的表达基因中,Cth、Gls2、Igf1 和 Nnmt 随着蛋白质摄入的增加而增加,而 Igf2bp2、Fgf21、Prkab2 和 Mtor 随着蛋白质摄入的减少而增加。膳食蛋白质对老年老鼠的肝脏基因表达有强大的影响,与先前报道的与长寿或热量限制调节有关的基因有一些重叠。