Literature DB >> 10725473

Species differences in peroxisome proliferation; mechanisms and relevance.

A I Choudhury1, S Chahal, A R Bell, S R Tomlinson, R A Roberts, A M Salter, D R Bell.   

Abstract

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 (PPARalpha). PPARalpha 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 PPARalpha 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 PPARalpha, and the guinea pig receptor has been characterised to be fully functional, as demonstrated in reporter gene expression assays. However, the guinea pig PPARalpha 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 PPARalpha as the principal determinant of species responsiveness. However, the demonstration that guinea pigs and humans undergo hypolipidaemia induced by PPARalpha-agonists calls into question the mode of action of PPARalpha agonists in "non-responsive" species.

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Year:  2000        PMID: 10725473     DOI: 10.1016/s0027-5107(99)00237-7

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  7 in total

1.  The PPAR-alpha activator fenofibrate fails to provide myocardial protection in ischemia and reperfusion in pigs.

Authors:  Ya Xu; Li Lu; Clifford Greyson; Mona Rizeq; Karin Nunley; Beata Wyatt; Michael R Bristow; Carlin S Long; Gregory G Schwartz
Journal:  Am J Physiol Heart Circ Physiol       Date:  2005-12-09       Impact factor: 4.733

2.  PPAR-gamma activation fails to provide myocardial protection in ischemia and reperfusion in pigs.

Authors:  Ya Xu; Michael Gen; Li Lu; Jennifer Fox; Sara O Weiss; R Dale Brown; Daniel Perlov; Hasan Ahmad; Peili Zhu; Clifford Greyson; Carlin S Long; Gregory G Schwartz
Journal:  Am J Physiol Heart Circ Physiol       Date:  2004-11-04       Impact factor: 4.733

Review 3.  Cytochrome P450 and xenobiotic receptor humanized mice.

Authors:  Frank J Gonzalez; Ai-Ming Yu
Journal:  Annu Rev Pharmacol Toxicol       Date:  2006       Impact factor: 13.820

4.  Organotypic modeling of human keratinocyte response to peroxisome proliferators.

Authors:  Carmen Zhang; Igor Gurevich; Brian J Aneskievich
Journal:  Cells Tissues Organs       Date:  2012-06-05       Impact factor: 2.481

5.  Zinc Fingers and Homeoboxes 2 (Zhx2) Regulates Sexually Dimorphic Cyp Gene Expression in the Adult Mouse Liver.

Authors:  Kate T Creasy; Jieyun Jiang; Hui Ren; Martha L Peterson; Brett T Spear
Journal:  Gene Expr       Date:  2016-05-17

Review 6.  The PPARα-dependent rodent liver tumor response is not relevant to humans: addressing misconceptions.

Authors:  J Christopher Corton; Jeffrey M Peters; James E Klaunig
Journal:  Arch Toxicol       Date:  2017-12-02       Impact factor: 5.153

7.  Current challenges and controversies in drug-induced liver injury.

Authors:  Alberto Corsini; Patricia Ganey; Cynthia Ju; Neil Kaplowitz; Dominique Pessayre; Robert Roth; Paul B Watkins; Mudher Albassam; Baolian Liu; Saray Stancic; Laura Suter; Michele Bortolini
Journal:  Drug Saf       Date:  2012-12-01       Impact factor: 5.606

  7 in total

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