Species differences in peroxisome proliferation; mechanisms and relevance

被引:40
作者
Choudhury, AI
Chahal, S
Bell, AR
Tomlinson, SR
Roberts, RA
Salter, AM
Bell, DR
机构
[1] Univ Nottingham, Sch Biol Sci, Nottingham NG7 2RD, England
[2] Astra Charnwood Safety Assessment, Loughborough LE11 5RH, Leics, England
[3] Zeneca Cent Toxicol Lab, Macclesfield SK10 4TJ, Cheshire, England
基金
英国惠康基金;
关键词
peroxisome proliferation-activated receptor alpha (PPAR alpha); pleiotropic response; peroxisome proliferators;
D O I
10.1016/S0027-5107(99)00237-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Peroxisome proliferators are a class of structurally diverse chemicals, which induce liver carcinogenesis in rodents through interaction and activation of the Peroxisome Proliferator-Activated Receptor alpha (PPAR alpha). PPAR alpha agonists elicit a powerful pleiotropic response, which include hypolipidaemia. We have examined the response of species that are classically unresponsive to peroxisome proliferators. Whereas hamster responds to PPAR alpha agonists by hepatomegaly and induction of marker genes, the guinea pig does not undergo hepatomegaly or induction of marker genes, such as CYP4A13. Both the hamster and the guinea pig have PPAR alpha, and the guinea pig receptor has been characterised to be fully functional. as demonstrated in reporter gene expression assays. However, the guinea pig PPAR alpha is expressed at low levels in liver, and the currently favoured hypothesis to explain species differences in hepatic peroxisome proliferation invokes the low level of PPAR alpha as the principal determinant of species responsiveness. However, the demonstration that guinea pigs and humans undergo hypolipidaemia induced by PPAR alpha-agonists calls into question the mode of action of PPAR alpha agonists in "non-responsive" species. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:201 / 212
页数:12
相关论文
共 78 条
[71]   The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools [J].
Thompson, JD ;
Gibson, TJ ;
Plewniak, F ;
Jeanmougin, F ;
Higgins, DG .
NUCLEIC ACIDS RESEARCH, 1997, 25 (24) :4876-4882
[72]  
TUCKER MJ, 1995, COMP TOXICOLOGY HYPO
[73]   A peroxisome proliferator-activated receptor-alpha (PPARα) cDNA cloned from guinea-pig liver encodes a protein with similar properties to the mouse PPARα:: implications for species differences in responses to peroxisome proliferators [J].
Tugwood, JD ;
Holden, PR ;
James, NH ;
Prince, RA ;
Roberts, RA .
ARCHIVES OF TOXICOLOGY, 1998, 72 (03) :169-177
[74]   Identification of a peroxisome proliferator-responsive element upstream of the human peroxisomal fatty acyl coenzyme A oxidase gene [J].
Varanasi, U ;
Chu, RY ;
Huang, Q ;
Castellon, R ;
Yeldandi, AV ;
Reddy, JK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (04) :2147-2155
[75]   PROLIFERATION OF MICROBODIES IN SACCHAROMYCES-CEREVISIAE [J].
VEENHUIS, M ;
MATEBLOWSKI, M ;
KUNAU, WH ;
HARDER, W .
YEAST, 1987, 3 (02) :77-84
[76]   FIBRATES INCREASE HUMAN APOLIPOPROTEIN A-II EXPRESSION THROUGH ACTIVATION OF THE PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR [J].
VUDAC, N ;
SCHOOJANS, K ;
KOSYKH, V ;
DALLONGEVILLE, J ;
FRUCHART, JC ;
STAELS, B ;
AUWERX, J .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (02) :741-750
[77]   The peroxisome proliferator (PP) response element upstream of the human acyl CoA oxidase gene is inactive among a sample human population: significance for species differences in response to PPs [J].
Woodyatt, NJ ;
Lambe, KG ;
Myers, KA ;
Tugwood, JD ;
Roberts, RA .
CARCINOGENESIS, 1999, 20 (03) :369-372
[78]   Role of peroxisome proliferator-activated receptor α in disease of pancreatic β cells [J].
Zhou, YT ;
Shimabukuro, M ;
Wang, MY ;
Lee, Y ;
Higa, M ;
Milburn, JL ;
Newgard, CB ;
Unger, RH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (15) :8898-8903