Literature DB >> 3356013

Kinetics of phenobarbital inhibition of intercellular communication in mouse hepatocytes.

R J Ruch1, J E Klaunig.   

Abstract

Gap junction-mediated intercellular communication in untreated and phenobarbital-treated C57BL/6 X C3H F1 mouse hepatocytes was evaluated by microinjection of fluorescent Lucifer Yellow CH dye. Intercellular communication (dye coupling) was detected in untreated hepatocytes after 0.5 h in culture, reached a maximum level in 24- and 48-h-old cultures (85.2%), and then decreased over the next 72 h. Phenobarbital (20-500 micrograms/ml) decreased dye coupling in a dose-related manner when added to freshly plated cultures. This inhibitory effect was evident during 0.5-12 h of treatment but was not seen in cultures treated for 24 h. Phenobarbital also decreased dye coupling within 30 min when added to established (24-h-old) hepatocyte cultures. This effect was maximal after 2 h treatment. In these cultures, dye coupling recovered within 15 min after removal of the promoter. Hepatocytes, pretreated with phenobarbital for 24 h, did not show inhibition of dye coupling after reapplication of phenobarbital. Thus, phenobarbital inhibited mouse hepatocyte dye coupling rapidly and reversibly, and the cells became refractory to the inhibitory effect after prolonged treatment.

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Year:  1988        PMID: 3356013

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  8 in total

1.  Re-establishment of gap junctional intercellular communication (GJIC) between human endometrial carcinomas by prostaglandin E(2).

Authors:  Scott R Schlemmer; David G Kaufman
Journal:  Exp Mol Pathol       Date:  2012-10-12       Impact factor: 3.362

2.  Methoxychlor and Vinclozolin Induce Rapid Changes in Intercellular and Intracellular Signaling in Liver Progenitor Cells.

Authors:  Pavel Babica; Rimma Zurabian; Esha R Kumar; Rajus Chopra; Maxwell J Mianecki; Joon-Suk Park; Libor Jaša; James E Trosko; Brad L Upham
Journal:  Toxicol Sci       Date:  2016-07-13       Impact factor: 4.849

3.  Iron potentiates acetaminophen-induced oxidative stress and mitochondrial dysfunction in cultured mouse hepatocytes.

Authors:  Mi Sun Moon; John P Richie; Harriet C Isom
Journal:  Toxicol Sci       Date:  2010-07-28       Impact factor: 4.849

4.  Nickel-induced increases in gap junctional communication in the uterine cell line SK-UT-1.

Authors:  M S Marty; R Loch-Caruso
Journal:  In Vitro Cell Dev Biol       Date:  1993-03

5.  Rat myometrial smooth muscle cells show high levels of gap junctional communication under a variety of culture conditions.

Authors:  R Loch-Caruso; M S Pahl; D R Juberg
Journal:  In Vitro Cell Dev Biol       Date:  1992-02

Review 6.  Cell culture assays for chemicals with tumor-promoting or tumor-inhibiting activity based on the modulation of intercellular communication.

Authors:  I V Budunova; G M Williams
Journal:  Cell Biol Toxicol       Date:  1994-04       Impact factor: 6.691

7.  Modifications of microfilaments and microtubules induced by two hepatic tumor promoters, phenobarbital and biliverdin in non-transformed and transformed hepatic cell lines.

Authors:  F Decloitre; C Lafarge-Frayssinet; M Martin; C Frayssinet
Journal:  Cell Biol Toxicol       Date:  1990-01       Impact factor: 6.691

Review 8.  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

  8 in total

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