Dietary restriction in aged mice can partially restore impaired metabolism of apolipoprotein A-IV and C-III

Sachiko Araki, S. Goto

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Dietary restriction (DR) is only one well-established non-genetic experimental means to retard aging in various species of animals. Here we demonstrated that DR in mice for 3months initiated late in life, at the age of 22months, partially restores age-related decline of serum apolipoprotein A-IV (apo A-IV) level and the gene expression found in the liver of ad libitum fed young animals as revealed by fasting. In contrast, increase in gene expression of apo C-III by fasting was higher in the aged than that in the young, but it was reduced to the level of young animals in DR counterparts of the aged. In view of the implication that apo A-IV and C-III are involved in the activation and inhibition of lipoprotein lipase, respectively, the adult onset DR can conceivably upregulate the activity of this enzyme that is likely reduced in aged animals and thus improve the lipid metabolism. The present findings suggest that DR initiated even relatively late in life may reduce risk of age-related diseases associated with impaired lipid metabolism.

Original languageEnglish
Pages (from-to)445-450
Number of pages6
JournalBiogerontology
Volume5
Issue number6
DOIs
Publication statusPublished - Nov 2004

Fingerprint

Apolipoproteins C
Lipid Metabolism
Fasting
Apolipoprotein C-III
Gene Expression
Lipoprotein Lipase
Up-Regulation
apolipoprotein A-IV
Liver
Enzymes
Serum

Keywords

  • Aging
  • Apolipoprotein A-IV
  • Apolipoprotein C-III
  • Dietary restriction
  • Fasting
  • Liver

ASJC Scopus subject areas

  • Geriatrics and Gerontology

Cite this

Dietary restriction in aged mice can partially restore impaired metabolism of apolipoprotein A-IV and C-III. / Araki, Sachiko; Goto, S.

In: Biogerontology, Vol. 5, No. 6, 11.2004, p. 445-450.

Research output: Contribution to journalArticle

@article{dfd2542efc2b47a59cf899ecbdb072cd,
title = "Dietary restriction in aged mice can partially restore impaired metabolism of apolipoprotein A-IV and C-III",
abstract = "Dietary restriction (DR) is only one well-established non-genetic experimental means to retard aging in various species of animals. Here we demonstrated that DR in mice for 3months initiated late in life, at the age of 22months, partially restores age-related decline of serum apolipoprotein A-IV (apo A-IV) level and the gene expression found in the liver of ad libitum fed young animals as revealed by fasting. In contrast, increase in gene expression of apo C-III by fasting was higher in the aged than that in the young, but it was reduced to the level of young animals in DR counterparts of the aged. In view of the implication that apo A-IV and C-III are involved in the activation and inhibition of lipoprotein lipase, respectively, the adult onset DR can conceivably upregulate the activity of this enzyme that is likely reduced in aged animals and thus improve the lipid metabolism. The present findings suggest that DR initiated even relatively late in life may reduce risk of age-related diseases associated with impaired lipid metabolism.",
keywords = "Aging, Apolipoprotein A-IV, Apolipoprotein C-III, Dietary restriction, Fasting, Liver",
author = "Sachiko Araki and S. Goto",
year = "2004",
month = "11",
doi = "10.1007/s10522-004-3202-7",
language = "English",
volume = "5",
pages = "445--450",
journal = "Biogerontology",
issn = "1389-5729",
publisher = "Springer Netherlands",
number = "6",

}

TY - JOUR

T1 - Dietary restriction in aged mice can partially restore impaired metabolism of apolipoprotein A-IV and C-III

AU - Araki, Sachiko

AU - Goto, S.

PY - 2004/11

Y1 - 2004/11

N2 - Dietary restriction (DR) is only one well-established non-genetic experimental means to retard aging in various species of animals. Here we demonstrated that DR in mice for 3months initiated late in life, at the age of 22months, partially restores age-related decline of serum apolipoprotein A-IV (apo A-IV) level and the gene expression found in the liver of ad libitum fed young animals as revealed by fasting. In contrast, increase in gene expression of apo C-III by fasting was higher in the aged than that in the young, but it was reduced to the level of young animals in DR counterparts of the aged. In view of the implication that apo A-IV and C-III are involved in the activation and inhibition of lipoprotein lipase, respectively, the adult onset DR can conceivably upregulate the activity of this enzyme that is likely reduced in aged animals and thus improve the lipid metabolism. The present findings suggest that DR initiated even relatively late in life may reduce risk of age-related diseases associated with impaired lipid metabolism.

AB - Dietary restriction (DR) is only one well-established non-genetic experimental means to retard aging in various species of animals. Here we demonstrated that DR in mice for 3months initiated late in life, at the age of 22months, partially restores age-related decline of serum apolipoprotein A-IV (apo A-IV) level and the gene expression found in the liver of ad libitum fed young animals as revealed by fasting. In contrast, increase in gene expression of apo C-III by fasting was higher in the aged than that in the young, but it was reduced to the level of young animals in DR counterparts of the aged. In view of the implication that apo A-IV and C-III are involved in the activation and inhibition of lipoprotein lipase, respectively, the adult onset DR can conceivably upregulate the activity of this enzyme that is likely reduced in aged animals and thus improve the lipid metabolism. The present findings suggest that DR initiated even relatively late in life may reduce risk of age-related diseases associated with impaired lipid metabolism.

KW - Aging

KW - Apolipoprotein A-IV

KW - Apolipoprotein C-III

KW - Dietary restriction

KW - Fasting

KW - Liver

UR - http://www.scopus.com/inward/record.url?scp=11244306346&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=11244306346&partnerID=8YFLogxK

U2 - 10.1007/s10522-004-3202-7

DO - 10.1007/s10522-004-3202-7

M3 - Article

VL - 5

SP - 445

EP - 450

JO - Biogerontology

JF - Biogerontology

SN - 1389-5729

IS - 6

ER -