CYP1A2 is not required for 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced immunosuppression
| Autor: | R. W. Setzer, Janet J. Diliberto, Linda S. Birnbaum, Ralph J. Smialowicz, Wanda C. Williams, Deborah E. Burgin |
|---|---|
| Rok vydání: | 2004 |
| Předmět: |
medicine.medical_specialty
Polychlorinated Dibenzodioxins Genotype Ratón medicine.medical_treatment Administration Oral Enzyme-Linked Immunosorbent Assay Hemolytic Plaque Technique Spleen Thymus Gland Toxicology Immunocompromised Host Mice Immune system Cytochrome P-450 CYP1A2 Internal medicine medicine Animals Immunosuppression Therapy Mice Knockout Dose-Response Relationship Drug biology CYP1A2 Antibody titer Cytochrome P450 Immunosuppression Organ Size Mice Inbred C57BL medicine.anatomical_structure Endocrinology Antibody Formation Toxicity biology.protein Environmental Pollutants Female Immunosuppressive Agents |
| Zdroj: | Toxicology. 197:15-22 |
| ISSN: | 0300-483X |
| DOI: | 10.1016/j.tox.2003.11.016 |
| Popis: | One of the most sensitive and reproducible immunotoxic endpoints of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) exposure is suppression of the antibody response to sheep red blood cells (SRBCs) in mice. Immunosuppression occurs in concert with hepatomegaly and associated induction of several hepatic cytochrome P450 enzymes, including CYP1A2 which is responsible for the hepatic sequestration of TCDD. In this study, TCDD-induced immunosuppression was evaluated in C57BL/6N CYP1A2 (+/+) wild-type and compared with that of age-matched CYP1A2 (-/-) knockout and CYP1A2 (+/-) heterozygous female mice. Groups of mice were given a single gavage dose of 0, 0.03, 0.1, 0.3, 1.0, 3.0 or 10.0microg TCDD/kg, followed 7 days later by immunization with SRBCs. Serum was obtained 5 days after immunization and body, spleen, thymus and liver weights were measured. sheep red blood cell (SRBC) antibody titers were determined by an enzyme-linked immunosorbent assay (ELISA). Anti-SRBC titers were suppressed at 1.0, 1.0 and 0.3microg TCDD/kg for CYP1A2 (+/+), CYP1A2 (+/-), and CYP1A2 (-/-) mice, respectively, which indicated a three-fold increase in TCDD-induced immunosuppression for the CYP1A2 (-/-) mice. This increase in TCDD-induced immunosuppression may be due to the inability of CYP1A2 (-/-) mice to sequester TCDD in the liver leading to a higher dose to the immune system. In CYP1A2 (+/+) mice, a dose of 3.0microg TCDD/kg was sufficient to increase the liver weight, while in CYP1A2 (-/-) mice no increase in liver weight was observed. Application of analysis of variance and dose-response modeling approaches indicate that there is little evidence that the immunosuppression dose-response curves, for the three strains, differ in the lower part of the dose-response range. Thus, CYP1A2 is not required for TCDD-induced immunosuppression in the mouse. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full Text from ScienceDirect