» Articles » PMID: 6521730

Sequential Alterations in the Micro-localization of Catalase in Mouse Liver After Treatment with Hypolipidemic Drugs

Overview
Publisher Springer
Specialty Biochemistry
Date 1984 Nov 1
PMID 6521730
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

A comparative study has been carried out on the micro-localization of catalase in mouse tissues subsequent to treatment with a representative range of hypolipidemic drugs. A commonality of effect was shown by clofibrate (ethyl-alpha-p-chlorophenoxyisobutyrate), Wy-14,643 (4-chloro-6-[2,3 xylidino)-2-pyrimidinylthio] acetic acid), RMI-15,414 (5-tetradecyloxy-2-furancarboxylic acid) and aspirin (acetyl salicylic acid), in that treatments with each of these drugs was associated with the release of peroxisomal catalase into the cytoplasmic compartment of liver and kidney. It was also noticeable that this increased cytosolic activity was characterized by the presence of an 'aged' form of the enzyme with different mobility and activity characteristics to that of the peroxisomal enzyme. Possible molecular bases for these effects and their relationship to peroxisomal biogenesis are discussed.

Citing Articles

Modification in oxidative stress, inflammation, and lipoprotein assembly in response to hepatocyte nuclear factor 4alpha knockdown in intestinal epithelial cells.

Marcil V, Seidman E, Sinnett D, Boudreau F, Gendron F, Beaulieu J J Biol Chem. 2010; 285(52):40448-60.

PMID: 20871093 PMC: 3003343. DOI: 10.1074/jbc.M110.155358.


IRAK-1 contributes to lipopolysaccharide-induced reactive oxygen species generation in macrophages by inducing NOX-1 transcription and Rac1 activation and suppressing the expression of antioxidative enzymes.

Maitra U, Singh N, Gan L, Ringwood L, Li L J Biol Chem. 2009; 284(51):35403-11.

PMID: 19850916 PMC: 2790969. DOI: 10.1074/jbc.M109.059501.


PPAR and liver injury in HIV-infected patients.

Lemoine M, Capeau J, Serfaty L PPAR Res. 2009; 2009:906167.

PMID: 19390649 PMC: 2669659. DOI: 10.1155/2009/906167.


On the compartmentalization of catalase, fatty acyl-CoA oxidase and urate oxidase in mammalian livers, and the influence of clofibrate treatment on this microlocalization.

Hemsley A, Pegg M, Crane D, Masters C Mol Cell Biochem. 1988; 83(2):187-94.

PMID: 3200253 DOI: 10.1007/BF00226146.


Changes to the integral membrane protein composition of mouse liver peroxisomes in response to the peroxisome proliferators clofibrate, Wy-14,643 and di(2-ethyl-hexyl)phthalate.

Crane D, Chen N, Masters C Mol Cell Biochem. 1988; 81(1):29-36.

PMID: 3173343 DOI: 10.1007/BF00225650.


References
1.
Appelkvist E, BRUNK U, Dallner G . Isolation of peroxisomes from rat liver using sucrose and Percoll gradients. J Biochem Biophys Methods. 1981; 5(4):203-17. DOI: 10.1016/0165-022x(81)90045-2. View

2.
Leighton F, Coloma L, Koenig C . Structure, composition, physical properties, and turnover of proliferated peroxisomes. A study of the trophic effects of Su-13437 on rat liver. J Cell Biol. 1975; 67(2PT.1):281-309. PMC: 2109608. DOI: 10.1083/jcb.67.2.281. View

3.
Crane D, Holmes R, MASTERS C . Synthesis and incorporation of phospholipid by peroxisomes of mouse liver. Biochim Biophys Acta. 1982; 712(1):57-64. DOI: 10.1016/0005-2760(82)90084-4. View

4.
Flatmark T, CHRISTIANSEN E, Kryvi H . Polydispersity of rat liver peroxisomes induced by the hypolipidemic and carcinogenic agent clofibrate. Eur J Cell Biol. 1981; 24(1):62-9. View

5.
Roels F . Cytochemical demonstration of extraperoxisomal catalase. I. Sheep liver. J Histochem Cytochem. 1976; 24(6):713-24. DOI: 10.1177/24.6.950458. View