Literature DB >> 6149920

Aging selectively alters glutathione S-transferase isozyme concentrations in liver and lung cytosol.

M E Spearman, K C Leibman.   

Abstract

The effects of aging on hepatic and pulmonary cytosolic glutathione S-transferase activities and concentrations were investigated in male Fischer 344 rats 3, 12, and 24 months old. Column isoelectric focusing of liver cytosol indicated that activities, measured with six epoxide substrates, of isozymes E, C, and B increased from 3 to 12 months of age and decreased from 3 to 24 months of age whereas activities of isozyme A were increased in the old group. With lung cytosol, activities of isozymes E, C, and B were decreased whereas isozyme A activities were increased in the old group. Purification to homogeneity of individual isozymes from liver and lung cytosol from each age group indicated that catalytic properties of isozymes were not altered by aging. Immunotitrations of hepatic and pulmonary cytosol from each age group showed that changes in the concentrations of these isozymes occurred with aging: heptic isozymes E, C, and B increased from 3 to 12 months of age and then decreased by 24 months of age, whereas isozymes A and AA were increased by 24 months of age. Pulmonary isozymes E, C, and B followed a pattern of decline from 3 to 24 months of age, whereas isozyme A concentrations were unchanged with increasing age. Analysis of these changes suggested that subunits Ya and Yc as one group and Yb and Y'b as another followed similar increases (from 3 to 12 months) and decreases (from 12 to 24 months) in the liver and that these subunits showed consistent decreases with age in the lung.

Entities:  

Mesh:

Substances:

Year:  1984        PMID: 6149920

Source DB:  PubMed          Journal:  Drug Metab Dispos        ISSN: 0090-9556            Impact factor:   3.922


  5 in total

1.  Developmental aspects of a unique glutathione S-transferase subunit Yx in the liver cytosol from rats with hereditary hyperbilirubinuria. Comparison with rat fetal liver transferase subunit Yfetus.

Authors:  T Igarashi; T Tsuchiya; Y Shikata; F Sagami; O Tagaya; T Horie; T Satoh
Journal:  Biochem J       Date:  1992-04-01       Impact factor: 3.857

2.  Ongoing hepatocellular regeneration and resiliency toward galactosamine hepatotoxicity.

Authors:  S K Abdul-Hussain; H M Mehendale
Journal:  Arch Toxicol       Date:  1992       Impact factor: 5.153

3.  Age-related loss of mitochondrial glutathione exacerbates menadione-induced inhibition of Complex I.

Authors:  Nicholas O Thomas; Kate P Shay; Tory M Hagen
Journal:  Redox Biol       Date:  2019-03-02       Impact factor: 11.799

4.  Glutathione maintenance mitigates age-related susceptibility to redox cycling agents.

Authors:  Nicholas O Thomas; Kate P Shay; Amanda R Kelley; Judy A Butler; Tory M Hagen
Journal:  Redox Biol       Date:  2016-09-22       Impact factor: 11.799

5.  Transcriptome analysis reveals mechanism underlying the differential intestinal functionality of laying hens in the late phase and peak phase of production.

Authors:  Wei-Wei Wang; Jing Wang; Hai-Jun Zhang; Shu-Geng Wu; Guang-Hai Qi
Journal:  BMC Genomics       Date:  2019-12-12       Impact factor: 3.969

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.