Literature DB >> 9720140

The quantitative distinction of hyperplasia from hypertrophy in hepatomegaly induced in the rat liver by phenobarbital.

P Carthew1, R E Edwards, B M Nolan.   

Abstract

A histological method utilizing the optical dissector principle has been developed for determining the absolute numbers of rat hepatocytes in the liver after treatment with phenobarbital (PB). The optical dissector is a technique derived from the "new stereology" used to measure the number of features, in this case hepatocyte nuclear profiles, that are present in a reference volume of tissue. The method has been applied to distinguish between the hepatomegaly that commonly occurs in rodents after treatment with chemicals, due to an increase in the number of cells caused by cell division (hyperplasia), rather than the size of cells (hypertrophy). In the case of PB treatment, the hepatomegaly was found to be partly due to hypertrophy and partly to hyperplasia after 2 weeks of treatment. While the increase in the absolute number of hepatocytes was not significant after 2 weeks, after 12 weeks of treatment with PB the number of hepatocytes was significantly increased, compared to the controls at that time point. PCNA labeling index measurements of liver hepatocytes confirmed that there was a significant increase in the growth fraction of hepatocytes during PB treatment. The induction of hyperplasia can be associated with an increased risk of eventual liver tumor formation, and the distinction of hyperplasia from hypertrophy, using a purely histological method, for the determination of increases in absolute hepatocyte cell numbers, will be useful in assessing whether treatment-related sustained hyperplasia is occurring in the liver, although this methodology could be applied to any organ.

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Year:  1998        PMID: 9720140     DOI: 10.1006/toxs.1998.2473

Source DB:  PubMed          Journal:  Toxicol Sci        ISSN: 1096-0929            Impact factor:   4.849


  8 in total

1.  Phenobarbital regulates nuclear expression of HNF-4alpha in mouse and rat hepatocytes independent of CAR and PXR.

Authors:  Aaron W Bell; George K Michalopoulos
Journal:  Hepatology       Date:  2006-07       Impact factor: 17.425

Review 2.  Human relevance of rodent liver tumour formation by constitutive androstane receptor (CAR) activators.

Authors:  Brian G Lake
Journal:  Toxicol Res (Camb)       Date:  2018-03-12       Impact factor: 3.524

3.  Nuclear receptor CAR (NR1I3) is essential for DDC-induced liver injury and oval cell proliferation in mouse liver.

Authors:  Yuichi Yamazaki; Rick Moore; Masahiko Negishi
Journal:  Lab Invest       Date:  2011-08-08       Impact factor: 5.662

4.  Liver-specific ablation of integrin-linked kinase in mice results in enhanced and prolonged cell proliferation and hepatomegaly after phenobarbital administration.

Authors:  Shashikiran Donthamsetty; William Bowen; Wendy Mars; Vishakha Bhave; Jian-Hua Luo; Cary Wu; Jennifer Hurd; Ann Orr; Aaron Bell; George Michalopoulos
Journal:  Toxicol Sci       Date:  2009-11-17       Impact factor: 4.849

Review 5.  Mode of action and human relevance analysis for nuclear receptor-mediated liver toxicity: A case study with phenobarbital as a model constitutive androstane receptor (CAR) activator.

Authors:  Clifford R Elcombe; Richard C Peffer; Douglas C Wolf; Jason Bailey; Remi Bars; David Bell; Russell C Cattley; Stephen S Ferguson; David Geter; Amber Goetz; Jay I Goodman; Susan Hester; Abigail Jacobs; Curtis J Omiecinski; Rita Schoeny; Wen Xie; Brian G Lake
Journal:  Crit Rev Toxicol       Date:  2013-11-04       Impact factor: 5.635

Review 6.  Prediction of the Carcinogenic Potential of Human Pharmaceuticals Using Repeated Dose Toxicity Data and Their Pharmacological Properties.

Authors:  Jan Willem van der Laan; Wenny H W Buitenhuis; Laura Wagenaar; Ans E M F Soffers; Eugene P van Someren; Cyrille A M Krul; Ruud A Woutersen
Journal:  Front Med (Lausanne)       Date:  2016-10-14

7.  An integrated functional genomic study of acute phenobarbital exposure in the rat.

Authors:  Claire L Waterman; Richard A Currie; Lisa A Cottrell; Jacky Dow; Jayne Wright; Catherine J Waterfield; Julian L Griffin
Journal:  BMC Genomics       Date:  2010-01-06       Impact factor: 3.969

8.  Triclocarban mediates induction of xenobiotic metabolism through activation of the constitutive androstane receptor and the estrogen receptor alpha.

Authors:  Mei-Fei Yueh; Tao Li; Ronald M Evans; Bruce Hammock; Robert H Tukey
Journal:  PLoS One       Date:  2012-06-15       Impact factor: 3.240

  8 in total

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