Mechanisms of spermidine-induced autophagy and geroprotection

被引:0
|
作者
Sebastian J. Hofer
Anna Katharina Simon
Martina Bergmann
Tobias Eisenberg
Guido Kroemer
Frank Madeo
机构
[1] Institute of Molecular Biosciences,Kennedy Institute of Rheumatology
[2] NAWI Graz,undefined
[3] University of Graz,undefined
[4] Field of Excellence BioHealth,undefined
[5] University of Graz,undefined
[6] BioTechMed Graz,undefined
[7] Centre de Recherche des Cordeliers,undefined
[8] Equipe labellisée par la Ligue contre le cancer,undefined
[9] Université de Paris Cité,undefined
[10] Sorbonne Université,undefined
[11] Inserm U1138,undefined
[12] Institut Universitaire de France,undefined
[13] Metabolomics and Cell Biology Platforms,undefined
[14] Institut Gustave Roussy,undefined
[15] University of Oxford,undefined
[16] Max Delbrück Center,undefined
[17] Institut du Cancer Paris CARPEM,undefined
[18] Department of Biology,undefined
[19] Hôpital Européen Georges Pompidou,undefined
[20] AP-HP,undefined
来源
Nature Aging | 2022年 / 2卷
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摘要
Aging involves the systemic deterioration of all known cell types in most eukaryotes. Several recently discovered compounds that extend the healthspan and lifespan of model organisms decelerate pathways that govern the aging process. Among these geroprotectors, spermidine, a natural polyamine ubiquitously found in organisms from all kingdoms, prolongs the lifespan of fungi, nematodes, insects and rodents. In mice, it also postpones the manifestation of various age-associated disorders such as cardiovascular disease and neurodegeneration. The specific features of spermidine, including its presence in common food items, make it an interesting candidate for translational aging research. Here, we review novel insights into the geroprotective mode of action of spermidine at the molecular level, as we discuss strategies for elucidating its clinical potential.
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页码:1112 / 1129
页数:17
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