Literature DB >> 3051140

Chemically induced proliferation of peroxisomes: implications for risk assessment.

W T Stott1.   

Abstract

An increasing number of beneficial and economically important drugs, industrial chemicals, and agrichemicals are being found to cause a dose-related hepatomegaly in rodent species which is associated with the proliferation of the subcellular organelle, the peroxisome. The prolonged proliferation of hepatocellular peroxisomes and the enhanced production of the normal peroxisomal metabolic byproduct, hydrogen peroxide, in these animals during chronic bioassays has been hypothesized to account for the tumorigenicity of several of these compounds, most of which lack any measurable genotoxicity in in vitro and in vivo assays. This paper briefly reviews the basic morphology and enzymology of the peroxisome and its relationship to specific pathologic changes in animals. The potential impact of the mechanism of action of peroxisome proliferators upon the design of toxicity studies and, in conjunction with interspecies sensitivity data, upon risk assessment is discussed.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 3051140     DOI: 10.1016/0273-2300(88)90026-8

Source DB:  PubMed          Journal:  Regul Toxicol Pharmacol        ISSN: 0273-2300            Impact factor:   3.271


  9 in total

Review 1.  The activation of beta-substituted nitrosamines that are carcinogenic to the pancreas.

Authors:  T Lawson; D Nagel; D Rogers
Journal:  Int J Pancreatol       Date:  1991-09

2.  Developmental toxicity of haloxyfop ethoxyethyl ester in the rat.

Authors:  K Machera
Journal:  Bull Environ Contam Toxicol       Date:  1993-10       Impact factor: 2.151

3.  Localization of the human soluble epoxide hydrolase gene (EPHX2) to chromosomal region 8p21-p12.

Authors:  C Larsson; I White; C Johansson; A Stark; J Meijer
Journal:  Hum Genet       Date:  1995-03       Impact factor: 4.132

4.  Morphological transformation and catalase activity of Syrian hamster embryo cells treated with hepatic peroxisome proliferators, TPA and nickel sulphate.

Authors:  S O Mikalsen; I Holen; T Sanner
Journal:  Cell Biol Toxicol       Date:  1990-01       Impact factor: 6.691

5.  Effects of clofibrate on lipids and fatty acids of mouse liver.

Authors:  G L Pennacchiotti; N P Rotstein; M I Aveldaño
Journal:  Lipids       Date:  1996-02       Impact factor: 1.880

6.  Metabolites of the plasticizer di(2-ethylhexyl)phthalate in urine samples of workers in polyvinylchloride processing industries.

Authors:  H A Dirven; P H van den Broek; A M Arends; H H Nordkamp; A J de Lepper; P T Henderson; F J Jongeneelen
Journal:  Int Arch Occup Environ Health       Date:  1993       Impact factor: 3.015

7.  The effects of perfluoro-octanoic acid on hepatic peroxisome proliferation and related parameters show no sex-related differences in mice.

Authors:  A K Sohlenius; K Andersson; J W DePierre
Journal:  Biochem J       Date:  1992-08-01       Impact factor: 3.857

Review 8.  Development of a physiologically based pharmacokinetic model of trichloroethylene and its metabolites for use in risk assessment.

Authors:  H J Clewell; P R Gentry; T R Covington; J M Gearhart
Journal:  Environ Health Perspect       Date:  2000-05       Impact factor: 9.031

9.  Significant increase of 8-hydroxydeoxyguanosine in liver DNA of rats following short-term exposure to the peroxisome proliferators di(2-ethylhexyl)phthalate and di(2-ethylhexyl)adipate.

Authors:  A Takagi; K Sai; T Umemura; R Hasegawa; Y Kurokawa
Journal:  Jpn J Cancer Res       Date:  1990-03
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.