共 203 条
Caloric restriction mimetics: towards a molecular definition
被引:180
作者:

Madeo, Frank
论文数: 0 引用数: 0
h-index: 0
机构:
Graz Univ, Inst Mol Biosci, A-8010 Graz, Austria Graz Univ, Inst Mol Biosci, A-8010 Graz, Austria

Pietrocola, Federico
论文数: 0 引用数: 0
h-index: 0
机构:
INSERM, Ctr Rech Cordeliers, Equipe Labellisee Ligue Natl Canc 11, F-75006 Paris, France
Univ Paris 05, Sorbonne Paris Cite, F-75006 Paris, France Graz Univ, Inst Mol Biosci, A-8010 Graz, Austria

Eisenberg, Tobias
论文数: 0 引用数: 0
h-index: 0
机构:
Graz Univ, Inst Mol Biosci, A-8010 Graz, Austria
INSERM, Ctr Rech Cordeliers, Equipe Labellisee Ligue Natl Canc 11, F-75006 Paris, France
Univ Paris 05, Sorbonne Paris Cite, F-75006 Paris, France Graz Univ, Inst Mol Biosci, A-8010 Graz, Austria

Kroemer, Guido
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Europeen Georges Pompidou, AP HP, Lab Immunooncol, F-75015 Paris, France Graz Univ, Inst Mol Biosci, A-8010 Graz, Austria
机构:
[1] Graz Univ, Inst Mol Biosci, A-8010 Graz, Austria
[2] INSERM, Ctr Rech Cordeliers, Equipe Labellisee Ligue Natl Canc 11, F-75006 Paris, France
[3] Univ Paris 05, Sorbonne Paris Cite, F-75006 Paris, France
[4] Hop Europeen Georges Pompidou, AP HP, Lab Immunooncol, F-75015 Paris, France
基金:
奥地利科学基金会;
欧洲研究理事会;
关键词:
LIFE-SPAN EXTENSION;
ATP-CITRATE-LYASE;
HISTONE ACETYLTRANSFERASE INHIBITOR;
GREEN TEA POLYPHENOL;
INDUCED INSULIN-RESISTANCE;
SKELETAL-MUSCLE;
DIETARY RESTRICTION;
METABOLIC SYNDROME;
GALLIC ACID;
POLYISOPRENYLATED BENZOPHENONE;
D O I:
10.1038/nrd4391
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Caloric restriction, be it constant or intermittent, is reputed to have health-promoting and lifespan-extending effects. Caloric restriction mimetics (CRMs) are compounds that mimic the biochemical and functional effects of caloric restriction. In this Opinion article, we propose a unifying definition of CRMs as compounds that stimulate autophagy by favouring the deacetylation of cellular proteins. This deacetylation process can be achieved by three classes of compounds that deplete acetyl coenzyme A (AcCoA; the sole donor of acetyl groups), that inhibit acetyl transferases (a group of enzymes that acetylate lysine residues in an array of proteins) or that stimulate the activity of deacetylases and hence reverse the action of acetyl transferases. A unifying definition of CRMs will be important for the continued development of this class of therapeutic agents.
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收藏
页码:727 / 740
页数:14
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