Literature DB >> 2030268

Influence of age and caloric restriction on expression of hepatic genes for xenobiotic and oxygen metabolizing enzymes in the mouse.

P L Mote1, J M Grizzle, R L Walford, S R Spindler.   

Abstract

The influence of age and life-span-prolonging caloric restriction on the expression of hepatic genes for xenobiotic and activated oxygen metabolism was investigated in female C3B10RF1 mice, a long-lived hybrid strain. Animals were fed either ad libitum, or diets reduced 20% or 52% in total calories but approximately unchanged in total protein, vitamins, and minerals. Cytochrome P1- and P3-450 (cyp1A1 and cyp1A2, respectively) mRNA levels decreased approximately 40% between age 4-5 months (young) and 30-31 months (old) in ad libitum fed animals (p less than or equal to .05). Caloric restriction eliminated this decrease. Manganese-superoxide dismutase mRNA decreased significantly in old ad libitum fed mice, and caloric restriction eliminated this decrease. No change in manganese-superoxide dismutase activity was detected, probably due to its low level and the large variability inherent in the assay. Catalase mRNA increased with age, but was not affected by diet. Catalase activity increased significantly with caloric restriction in young and old mice, in the absence of an increase in catalase mRNA, suggesting translational or posttranslational effects. CuZn-superoxide dismutase, glutathione peroxidase and epoxide hydrolase mRNA, and the ratio of ribosomal to total mRNA did not change with age or diet.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 2030268     DOI: 10.1093/geronj/46.3.b95

Source DB:  PubMed          Journal:  J Gerontol        ISSN: 0022-1422


  6 in total

1.  Changes in gene expression associated with aging commonly originate during juvenile growth.

Authors:  Julian C Lui; Weiping Chen; Kevin M Barnes; Jeffrey Baron
Journal:  Mech Ageing Dev       Date:  2010-09-09       Impact factor: 5.432

2.  Antioxidative mechanisms and plasma growth hormone levels: potential relationship in the aging process.

Authors:  H M Brown-Borg; A M Bode; A Bartke
Journal:  Endocrine       Date:  1999-08       Impact factor: 3.633

3.  Genomic profiling of short- and long-term caloric restriction effects in the liver of aging mice.

Authors:  S X Cao; J M Dhahbi; P L Mote; S R Spindler
Journal:  Proc Natl Acad Sci U S A       Date:  2001-09-04       Impact factor: 11.205

4.  Life-long caloric restriction reduces oxidative stress and preserves nitric oxide bioavailability and function in arteries of old mice.

Authors:  Anthony J Donato; Ashley E Walker; Katherine A Magerko; R Colton Bramwell; Alex D Black; Grant D Henson; Brooke R Lawson; Lisa A Lesniewski; Douglas R Seals
Journal:  Aging Cell       Date:  2013-07-02       Impact factor: 9.304

5.  Increased effective activity of rat liver catalase by dietary restriction.

Authors:  R J Feuers; R Weindruch; J E Leakey; P H Duffy; R W Hart
Journal:  Age (Omaha)       Date:  1997-10

6.  Complete amino acid sequence of Proteus mirabilis PR catalase. Occurrence of a methionine sulfone in the close proximity of the active site.

Authors:  A Buzy; V Bracchi; R Sterjiades; J Chroboczek; P Thibault; J Gagnon; H M Jouve; G Hudry-Clergeon
Journal:  J Protein Chem       Date:  1995-02
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.