Literature DB >> 1293309

Perfluorooctanoic acid has persistent effects on peroxisome proliferation and related parameters in mouse liver.

A K Sohlenius1, B Lundgren, J W DePierre.   

Abstract

Male C57Bl/6 mice were treated for 5 days with 0.05% perfluorooctanoic acid (PFOA) in their diet. This treatment resulted in a potent induction of peroxisomal fatty acid beta-oxidation in the liver. In order to investigate recovery from treatment with PFOA, mice were given normal laboratory chow for up to 20 days after termination of PFOA administration. It was established that the activities of peroxisomal lauoryl-CoA oxidase and palmitoyl-CoA oxidation were still elevated 2-3 weeks after termination of treatment. The catalase activity recovered in the cytosolic fraction was also still significantly elevated after 20 days with normal laboratory chow. Furthermore, the protein content of the mitochondrial fraction was increased by PFOA and had not returned to control level at the end of the recovery period. Perfluorooctanoic acid also caused a persistent effect in omega hydroxylation of lauric acid (cytochrome P-452). The activities of cytosolic DT-diaphorase and glutathione transferase were also enhanced by PFOA. However, these two enzymes recovered relatively rapidly from the treatment (2-20 days). This study reveals two different patterns of recovery from PFOA treatment, one involving parameters that recovered completely, or almost completely, from PFOA treatment after 20 days and another involving parameters that were still elevated at the end of the recovery period.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1293309     DOI: 10.1002/jbt.2570070403

Source DB:  PubMed          Journal:  J Biochem Toxicol        ISSN: 0887-2082


  7 in total

1.  Effects of peroxisome proliferators on the thymus and spleen of mice.

Authors:  Q Yang; Y Xie; J W Depierre
Journal:  Clin Exp Immunol       Date:  2000-11       Impact factor: 4.330

2.  Characterization of the adipose tissue atrophy induced by peroxisome proliferators in mice.

Authors:  Yi Xie; Qian Yang; B Dean Nelson; Joseph W DePierre
Journal:  Lipids       Date:  2002-02       Impact factor: 1.880

3.  Hepatic and renal Bcrp transporter expression in mice treated with perfluorooctanoic acid.

Authors:  Lobna M Eldasher; Xia Wen; Michael S Little; Kristin M Bircsak; Lindsay L Yacovino; Lauren M Aleksunes
Journal:  Toxicology       Date:  2013-02-19       Impact factor: 4.221

4.  Structure and expression of a cluster of glutathione S-transferase genes from a marine fish, the plaice (Pleuronectes platessa).

Authors:  M J Leaver; J Wright; S G George
Journal:  Biochem J       Date:  1997-01-15       Impact factor: 3.857

5.  1H NMR-Based Metabolomic Analysis of Sub-Lethal Perfluorooctane Sulfonate Exposure to the Earthworm, Eisenia fetida, in Soil.

Authors:  Brian P Lankadurai; Vasile I Furdui; Eric J Reiner; André J Simpson; Myrna J Simpson
Journal:  Metabolites       Date:  2013-08-27

6.  Analysis of Sub-Lethal Toxicity of Perfluorooctane Sulfonate (PFOS) to Daphnia magna Using ¹H Nuclear Magnetic Resonance-Based Metabolomics.

Authors:  Martha N Kariuki; Edward G Nagato; Brian P Lankadurai; André J Simpson; Myrna J Simpson
Journal:  Metabolites       Date:  2017-04-14

7.  Genomic profiling reveals an alternate mechanism for hepatic tumor promotion by perfluorooctanoic acid in rainbow trout.

Authors:  Susan C Tilton; Gayle A Orner; Abby D Benninghoff; Hillary M Carpenter; Jerry D Hendricks; Cliff B Pereira; David E Williams
Journal:  Environ Health Perspect       Date:  2008-08       Impact factor: 9.031

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.