Time- and Concentration-Dependent Induction of CYP1A1 and CYP1A2 in Precision-Cut Rat Liver Slices Incubated in Dynamic Organ Culture in the Presence of 2,3,7,8-Tetrachlorodibenzo-p-Dioxin

• Published in: Toxicology and applied pharmacology Vol. 155; no. 2; pp. 127 - 138
• Main Authors: Drahushuk, Adam T., McGarrigle, Barbara P., Slezak, Brian P., Stegeman, John J., Olson, James R.
• Format: Journal Article
• Language: English
• Published: San Diego, CA Elsevier Inc 01.03.1999; Elsevier
• Subjects: Animals; Biological and medical sciences; Chemical and industrial products toxicology. Toxic occupational diseases; Cytochrome P-450 CYP1A1 - biosynthesis; Cytochrome P-450 CYP1A2 - biosynthesis; Dose-Response Relationship, Drug; Environmental Pollutants - pharmacology; Enzyme Induction - drug effects; Immunohistochemistry; Liver - drug effects; Liver - enzymology; Male; Medical sciences; Organ Culture Techniques; Polychlorinated Dibenzodioxins - pharmacology; Rats; Rats, Sprague-Dawley; Time Factors; Toxicology; Various organic compounds; Culture medium; Rat; Isozyme; Toxicity; Cytochrome P450; Rodentia; Hepatic disease; Time response relation; In vitro; Histological section; Dose activity relation; Vertebrata; Mammalia; Ultrastructure; Animal; Digestive diseases; Models
• ISSN: 0041-008X; 1096-0333
• DOI: 10.1006/taap.1998.8578

In a previous 24-h study, precision-cut rat liver slices were validated as a usefulin vitromodel for assessing the dose-related induction of CYP1A1 and CYP1A2 in rat liver following exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Further assessment of the utility of this model was accomplished by initially exposing rat liver slices to medium containing TCDD (0.01 nM) for 24 h and incubating the slices up to an additional 72 h in TCDD-free medium. The slices remained viable throughout the incubation period with an intracellular potassium content varying from 45.2 ± 2.3 μmol/g at 48 h to 50.0 ± 1.6 μmol/g at 72 h. In TCDD-exposed slices, CYP1A1 protein and its respective enzymatic activity, theO-deethylation of ethoxyresorufin (EROD), significantly increased with time over the 96-h incubation period, with EROD activity increasing from 63.6 ± 14.2 at 24 h to 905 ± 291 pmol/mg/min at 96 h. Under identical incubation conditions, but in the absence of TCDD, the EROD activity for the control liver slices ranged from 14.3 ± 4.3 to 44.9 ± 11.9 pmol/min/mg. Conversely, the level of CYP1A2 protein and its respective activity (acetanilide hydroxylation) transiently decreased from 24 to 96 h with no significant differences observed between the control (0 nM TCDD) and treatment group (0.01 nM TCDD). The concentration–effect relationship at 96 h was characterized by incubating rat liver slices for the initial 24 h in medium containing TCDD at concentrations ranging from 0.1 pM to 10 nM. Induction of CYP1A1 protein and EROD activity was observed for all treatment groups with the 10 nM TCDD treatment group displaying greater than 100-fold induction compared to control (0 nM TCDD). Immunohistochemical localization of CYP1A1 protein within liver slices supported the time- and concentration-dependent induction of EROD activity by TCDD. The induction of CYP1A1 was initially observed to be centrilobular, with increased expression due to both elevated CYP1A1 within cells and the recruitment of additional cells expressing CYP1A1 throughout the entire liver slice. Additionally, the immunohistochemical analysis of the liver slices demonstrated the conservation of tissue architecture following up to 96 h of incubation in dynamic organ culture and provided further evidence for maintenance of tissue viability. In comparison to CYP1A1, the induction of CYP1A2 at 96 h was a less sensitive response, with significant induction of CYP1A2 protein and its respective activity occurring at a medium concentration of 0.1 nM TCDD (686 pg/g liver). In general, increasing the incubation period from 24 to 96 h markedly increased TCDD-induced expression of CYP1A1 and minimally enhanced CYP1A2 expression. Moreover, extending the incubation period to 96 h resulted inin vitroinduction profiles for CYP1A1 and CYP1A2 that were qualitatively and quantitatively similar to that previously observed followingin vivoexposure to TCDD (Drahushuket al., Toxicol. Appl. Pharmacol.140, 393–403, 1996).