Glycine supplementation extends lifespan of male and female mice.
Adenomatosis, Pulmonary
/ epidemiology
Aging
/ drug effects
Animals
Aspirin
/ pharmacology
Diet
Dietary Supplements
Female
Glycine
/ pharmacology
Inulin
/ pharmacology
Longevity
/ drug effects
Male
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Piperazines
/ pharmacology
para-Aminobenzoates
/ pharmacology
anti-aging
life span
longevity regulation
Journal
Aging cell
ISSN: 1474-9726
Titre abrégé: Aging Cell
Pays: England
ID NLM: 101130839
Informations de publication
Date de publication:
06 2019
06 2019
Historique:
received:
28
09
2018
revised:
01
01
2019
accepted:
23
01
2019
pubmed:
28
3
2019
medline:
27
6
2020
entrez:
28
3
2019
Statut:
ppublish
Résumé
Diets low in methionine extend lifespan of rodents, though through unknown mechanisms. Glycine can mitigate methionine toxicity, and a small prior study has suggested that supplemental glycine could extend lifespan of Fischer 344 rats. We therefore evaluated the effects of an 8% glycine diet on lifespan and pathology of genetically heterogeneous mice in the context of the Interventions Testing Program. Elevated glycine led to a small (4%-6%) but statistically significant lifespan increase, as well as an increase in maximum lifespan, in both males (p = 0.002) and females (p < 0.001). Pooling across sex, glycine increased lifespan at each of the three independent sites, with significance at p = 0.01, 0.053, and 0.03, respectively. Glycine-supplemented females were lighter than controls, but there was no effect on weight in males. End-of-life necropsies suggested that glycine-treated mice were less likely than controls to die of pulmonary adenocarcinoma (p = 0.03). Of the 40 varieties of incidental pathology evaluated in these mice, none were increased to a significant degree by the glycine-supplemented diet. In parallel analyses of the same cohort, we found no benefits from TM5441 (an inhibitor of PAI-1, the primary inhibitor of tissue and urokinase plasminogen activators), inulin (a source of soluble fiber), or aspirin at either of two doses. Our glycine results strengthen the idea that modulation of dietary amino acid levels can increase healthy lifespan in mice, and provide a foundation for further investigation of dietary effects on aging and late-life diseases.
Identifiants
pubmed: 30916479
doi: 10.1111/acel.12953
pmc: PMC6516426
doi:
Substances chimiques
Piperazines
0
TM5441
0
para-Aminobenzoates
0
Inulin
9005-80-5
Aspirin
R16CO5Y76E
Glycine
TE7660XO1C
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
e12953Subventions
Organisme : NCI NIH HHS
ID : P30 CA034196
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL051387
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG028740
Pays : United States
Organisme : NIA NIH HHS
ID : U01 AG022308
Pays : United States
Organisme : NIA NIH HHS
ID : R24 AG047115
Pays : United States
Organisme : NIA NIH HHS
ID : U01 AG022307
Pays : United States
Organisme : NIA NIH HHS
ID : U01 AG022303
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG024824
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG013319
Pays : United States
Informations de copyright
© 2019 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd.
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