Literature DB >> 16010866

Influence of different calcic antagonists on the Caco-2 cell monolayer integrity or "TEER, a measurement of toxicity?".

F Mathieu1, M J Galmier, J F Pognat, C Lartigue.   

Abstract

The purpose of this work was to investigate the interest of the TEER measurement, a quite simple measure, as an evaluation of toxicity, in function of time and level of drug in the experimental medium, for different anticalcic agents. The extend of the increase and decrease of TEER, was evaluated by measuring the TEERmax and calculating the TEER50 respectively. Three groups of compounds could be therefore considered. The first, characterized by a quite short period of TEER increase, followed by an extremely rapid decrease (high values of TEER50), included perhexiline and prenylamine. The most toxic compounds, the second one, characterized by the smallest variations of TEER, included verapamil and diltiazem. This group was related with the less toxic compounds, the third group, represented by bepridil, characterized by dependant-dose TEERmax and TEER50. Therefore, the TEER measurement appeared as a quite simple approach of comparative toxicity of anticalcic agents.

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Year:  2005        PMID: 16010866     DOI: 10.1007/BF03226412

Source DB:  PubMed          Journal:  Eur J Drug Metab Pharmacokinet        ISSN: 0378-7966            Impact factor:   2.441


  16 in total

1.  Assessment of the marine toxins by monitoring the integrity of human intestinal Caco-2 cell monolayers.

Authors:  T Okada; A Narai; S Matsunaga; N Fusetani; M Shimizu
Journal:  Toxicol In Vitro       Date:  2000-06       Impact factor: 3.500

2.  Transepithelial transport of bepridil in the human intestinal cell line, Caco-2, using a "dynamic model".

Authors:  F Mathieu; M J Galmier; A Nicolay; J F Pognat; C Lartigue
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2003 Apr-Jun       Impact factor: 2.441

3.  Epithelial transport of drugs in cell culture. II: Effect of extracellular calcium concentration on the paracellular transport of drugs of different lipophilicities across monolayers of intestinal epithelial (Caco-2) cells.

Authors:  P Artursson; C Magnusson
Journal:  J Pharm Sci       Date:  1990-07       Impact factor: 3.534

4.  An oligopeptide permeates intestinal tight junctions at glucose-elicited dilatations. Implications for oligopeptide absorption.

Authors:  K Atisook; J L Madara
Journal:  Gastroenterology       Date:  1991-03       Impact factor: 22.682

5.  Modulation of the tight junctions of the Caco-2 cell monolayers by H2-antagonists.

Authors:  L S Gan; S Yanni; D R Thakker
Journal:  Pharm Res       Date:  1998-01       Impact factor: 4.200

6.  Transepithelial transport of bepridil in the human intestinal cell line, Caco-2, using two media, DMEMc and HBSS.

Authors:  F Mathieu; M J Galmier; J F Pognat; J Petit; C Lartigue
Journal:  Int J Pharm       Date:  1999-04-30       Impact factor: 5.875

7.  Water handling in Caco-2 cells: effects of acidification of the medium.

Authors:  M Parisi; E Escobar; C Huet; P Ripoche; D Louvard; J Bourguet
Journal:  Pflugers Arch       Date:  1993-04       Impact factor: 3.657

8.  Regulation of paracellular permeability in Caco-2 cell monolayers by protein kinase C.

Authors:  W F Stenson; R A Easom; T E Riehl; J Turk
Journal:  Am J Physiol       Date:  1993-11

9.  Effects of chlorinated amines on endothelial and epithelial barriers in vitro and ex vivo.

Authors:  D M Shasby; F Hampson
Journal:  Exp Lung Res       Date:  1989-05       Impact factor: 2.459

10.  Increases in guinea pig small intestinal transepithelial resistance induced by osmotic loads are accompanied by rapid alterations in absorptive-cell tight-junction structure.

Authors:  J L Madara
Journal:  J Cell Biol       Date:  1983-07       Impact factor: 10.539

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