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PMID: 12044962 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Dietary restriction reduces atherosclerosis and oxidative stress in the aorta of apolipoprotein E-deficient mice.

Mechanisms of ageing and development ·Vol. 123 ·No. 8 ·2002-04-30 ·Pages 1121-31

Guo Z, Mitchell-Raymundo F, Yang H, Ikeno Y, Nelson J, Diaz V, Richardson A, Reddick R

Abstract

Dietary restriction (DR) has been shown to inhibit almost all the age-related diseases, e.g. cardiomyopathy and cancers, in rodents. However, there is little information for the effect of DR on atherosclerosis. In the present study, we examined the effect of DR on the development of atherosclerosis in mice homozygous knockout for apolipoprotein E gene (ApoE(-/-)). The ApoE(-/-) mice were fed either ad libitum (AL) or 60% of the diet consumed by the mice fed AL. Atherosclerotic lesions in the proximal aorta of these mice were measured. Our results showed that ApoE(-/-) mice fed the calorie-restricted diet had smaller and relatively early stages of atherosclerotic lesions (e.g. foam cells and free lipids) when compared to ApoE(-/-) mice fed AL, who developed more advanced lesions (e.g. fibrous caps and acellular areas). In addition, ApoE(-/-) mice fed the calorie-restricted diet showed a significant decrease in the level of lipid hydroperoxides and the production of superoxide and hydrogen peroxide in the aorta as compared to ApoE(-/-) mice fed AL. These observations suggest that reduction of oxidative stress in the arterial wall may contribute to the anti-atherogenic effect of DR in ApoE(-/-) mice.

MeSH Terms
Animals Aorta/metabolism,pathology Apolipoproteins E/genetics,metabolism Arteriosclerosis/metabolism,pathology Cholesterol/blood Diet Disease Models, Animal Energy Intake Hydrogen Peroxide/metabolism Lipid Peroxidation Lipoproteins, LDL/metabolism Male Mice Mice, Knockout Oxidative Stress Superoxides/metabolism
Chemicals
Apolipoproteins E Lipoproteins, LDL oxidized low density lipoprotein Superoxides Cholesterol Hydrogen Peroxide
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Guo ZhongMao
Department of Physiology, University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, San Antonio, TX 78229, USA. zguo@mmx.edu
Mitchell-Raymundo Felicia
Yang Hong
Ikeno Yuji
Nelson James
Diaz Vivian
Richardson Arlan
Reddick Robert
Article Info
Journal
Mechanisms of ageing and development
Abbr.
Mech Ageing Dev
ISSN
0047-6374
Published
2002-04-30
Pages
1121-31
Language
English
Region
Ireland
NLM ID
0347227
Subset
IM
Grants
NIA NIH HHS · AG 16998 · United States
NIA NIH HHS · P01 AG13319 · United States
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