TY - JOUR
T1 - Immunosuppressive effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin in strains of mice with different susceptibility to induction of aryl hydrocarbon hydroxylase
AU - Vecchi, Annunciata
AU - Sironi, Marina
AU - Canegrati, Maria Antonia
AU - Recchia, Martino
AU - Garattini, Silvio
PY - 1983
Y1 - 1983
N2 - Mouse strains with different susceptibility to aryl hydrocarbon hydroxylase (AHH) induction and with different levels and/or affinity for a specific cytosolic binding protein ("receptor") were used to investigate the immunosuppressive effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Humoral antibody production was strongly inhibited in C57B1 6 and C3H HeN mice (more susceptible strains) with very low, single doses of TCDD (1.2 μg/kg), while other strains ( DBA 2 and AKR) required higher doses (at least 6 μg/kg) to be partially suppressed. Longer exposure (8 weeks) did not increase the sensitivity of DBA 2 mice. A good correlation between the degree of enzyme inducibility and immunosuppression was observed in studies with B6D2F1 mice and backcrosses. Similar results were obtained with 2,3,7,8-tetrachlorodibenzo-furan (TCDF), the most powerful competitor for TCDD "receptor" in vitro and in vivo. TCDD immnotoxic effects appeared to be associated with the presence of a specific cytosolic binding protein which mediates AHH induction.
AB - Mouse strains with different susceptibility to aryl hydrocarbon hydroxylase (AHH) induction and with different levels and/or affinity for a specific cytosolic binding protein ("receptor") were used to investigate the immunosuppressive effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Humoral antibody production was strongly inhibited in C57B1 6 and C3H HeN mice (more susceptible strains) with very low, single doses of TCDD (1.2 μg/kg), while other strains ( DBA 2 and AKR) required higher doses (at least 6 μg/kg) to be partially suppressed. Longer exposure (8 weeks) did not increase the sensitivity of DBA 2 mice. A good correlation between the degree of enzyme inducibility and immunosuppression was observed in studies with B6D2F1 mice and backcrosses. Similar results were obtained with 2,3,7,8-tetrachlorodibenzo-furan (TCDF), the most powerful competitor for TCDD "receptor" in vitro and in vivo. TCDD immnotoxic effects appeared to be associated with the presence of a specific cytosolic binding protein which mediates AHH induction.
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U2 - 10.1016/0041-008X(83)90288-0
DO - 10.1016/0041-008X(83)90288-0
M3 - Article
C2 - 6857677
AN - SCOPUS:0020581122
SN - 0041-008X
VL - 68
SP - 434
EP - 441
JO - Toxicology and Applied Pharmacology
JF - Toxicology and Applied Pharmacology
IS - 3
ER -