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PMID: 1409611 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Protein oxidation associated with aging is reduced by dietary restriction of protein or calories.

Youngman LD, Park JY, Ames BN

Abstract

The accumulation of unrepaired oxidative damage products may be a major factor in cellular aging. Both oxidative lesions in DNA and oxidatively damaged proteins have been shown to accumulate during aging. The accumulation of oxidized proteins in Fischer 344 rats was compared for animals consuming protein-restricted and calorically restricted diets--both of which have been shown to extend lifespan. Rats were fed diets restricted in either protein (5% or 10% of the diet as compared with the normal 20% casein), or calories (25% or 40% less than normal), or total diet (40% less than normal). In addition, some of the rats fed a diet providing 5% or 20% protein were irradiated twice weekly (125 rads per exposure; 1 rad = 0.01 Gy). The level of oxidative damage to proteins (protein carbonyls) was determined in rats sacrificed at various times. The oxidative damage to proteins increased with aging and with radiation. Either protein or calorie restriction markedly inhibited the accumulation of oxidatively damaged proteins. Protein restriction reduced the accumulation of oxidatively damaged proteins during the oxidative stress of chronic irradiation.

MeSH Terms
Aging/physiology Animals Body Weight Diet, Reducing Dietary Proteins Energy Intake Male Oxidation-Reduction Protein-Energy Malnutrition/physiopathology Proteins/metabolism,radiation effects Rats Rats, Inbred F344
Chemicals
Dietary Proteins Proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Youngman L D
Division of Biochemistry and Molecular Biology, University of California, Berkeley 94720.
Park J Y
Ames B N
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1992-10-01
Pages
9112-6
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC50075
Subset
IM
Grants
NCI NIH HHS · CA39910 · United States
NIEHS NIH HHS · ESO1896 · United States
Corrections
ErratumIn
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