TY - JOUR
T1 - 2-nitrofluorene metabolism in rat lung. Pharmacokinetic and metabolic effects of β-naphthoflavone treatment
AU - Törnquist, S.
AU - Möller, L.
AU - Gabrielsson, J.
AU - Gustafsson, J. å
AU - Toftgård, R.
N1 - Funding Information:
Lars Nybom is gratefully acknowledged for skilful technical assistance. We thank Tapio Haaparanta for providing the anti-P450 antisera. This investigation was supported by the National Swedish Environmental Protection Board, the Swedish Cancer Society, the Swedish Academy of Pharmaceutical Science and the Swedish Tobacco Company.
Copyright:
Copyright 2010 Elsevier B.V., All rights reserved.
PY - 1990/8
Y1 - 1990/8
N2 - Absorption, metabolism and DNA binding of 2-nitrofluorene (NF) was studied in isolated, perfused and ventilated rat lungs and in lung microsomal incubations. Comparisons were made between control animals and animals treated with β-naphthoflavone (BNF), a 2,3,7,8-tetrachlorodibenzo(p)dioxin (TCDD) receptor ligand and inducer of cytochrome P450IA1. Clearance of NF increased significantly in the isolated, perfused and ventilated lungs after BNF dosage, from 0.55 ± 0.06 ml/min to 2.37 ±0.62 ml/min (P < 0.05, n = 5-6). As a consequence of this, the mean residence time (MRT) for NF decreased when NF was dosed directly to the perfusion buffer, from 213 ±23 min (n = 6) to 48 ±9 min (n = 6), and after intratracheal dosage from 289 ±101 min (n = 5) to 135 ±72 min (n = 5). Irreversible binding of NF metabolites to DNA increased 2-fold after treatment with BNF when NF was dosed to the lung perfusion buffer. Treatment with BNF increased the rate of lung microsomal NF metabolism significantly, from 54 ±5 to 106 ±11 pmol/min/mg protein (P < 0.05, n = 6-12). Formation of the monohydroxylated metabolite X-OHNF was inhibited in vitro by addition of α-naphthoflavone (50 μM), by 89 and 98% with lung microsomal fractions from control and BNF-treated rats respectively. In contrast, proadifen (50 μM) preferentially inhibited formation of 9-OHNF, by 42 and 33% in incubations with lung microsomal fractions from control and BNF-treated animals. Anti-P450IIB1-IgG inhibited formation of 9-OHNF by 96 and 45% with lung microsomes from control and BNF-treated rats respectively. Formation of X-OHNF was unaffected by addition of anti-P-450IIB1-IgG in both cases. These results show that both constitutive and inducible microsomal rat lung enzymes metabolize NF. A constitutive enzyme, most likely cytochrome P450IIB1, catalyzes metabolic attack on NF with high preference for the 9-position. A BNF-inducible microsomal enzyme, most likely cytochrome P450IA1, catalyzes hydroxylation of NF both in the 9-position and in other positions. Increased metabolic clearance, metabolism and DNA binding of NF after BNF treatment suggest that the level and specificity of cytochrome P450 isozymes may be important determinants for toxicity and availability of NF in the rat lung.
AB - Absorption, metabolism and DNA binding of 2-nitrofluorene (NF) was studied in isolated, perfused and ventilated rat lungs and in lung microsomal incubations. Comparisons were made between control animals and animals treated with β-naphthoflavone (BNF), a 2,3,7,8-tetrachlorodibenzo(p)dioxin (TCDD) receptor ligand and inducer of cytochrome P450IA1. Clearance of NF increased significantly in the isolated, perfused and ventilated lungs after BNF dosage, from 0.55 ± 0.06 ml/min to 2.37 ±0.62 ml/min (P < 0.05, n = 5-6). As a consequence of this, the mean residence time (MRT) for NF decreased when NF was dosed directly to the perfusion buffer, from 213 ±23 min (n = 6) to 48 ±9 min (n = 6), and after intratracheal dosage from 289 ±101 min (n = 5) to 135 ±72 min (n = 5). Irreversible binding of NF metabolites to DNA increased 2-fold after treatment with BNF when NF was dosed to the lung perfusion buffer. Treatment with BNF increased the rate of lung microsomal NF metabolism significantly, from 54 ±5 to 106 ±11 pmol/min/mg protein (P < 0.05, n = 6-12). Formation of the monohydroxylated metabolite X-OHNF was inhibited in vitro by addition of α-naphthoflavone (50 μM), by 89 and 98% with lung microsomal fractions from control and BNF-treated rats respectively. In contrast, proadifen (50 μM) preferentially inhibited formation of 9-OHNF, by 42 and 33% in incubations with lung microsomal fractions from control and BNF-treated animals. Anti-P450IIB1-IgG inhibited formation of 9-OHNF by 96 and 45% with lung microsomes from control and BNF-treated rats respectively. Formation of X-OHNF was unaffected by addition of anti-P-450IIB1-IgG in both cases. These results show that both constitutive and inducible microsomal rat lung enzymes metabolize NF. A constitutive enzyme, most likely cytochrome P450IIB1, catalyzes metabolic attack on NF with high preference for the 9-position. A BNF-inducible microsomal enzyme, most likely cytochrome P450IA1, catalyzes hydroxylation of NF both in the 9-position and in other positions. Increased metabolic clearance, metabolism and DNA binding of NF after BNF treatment suggest that the level and specificity of cytochrome P450 isozymes may be important determinants for toxicity and availability of NF in the rat lung.
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U2 - 10.1093/carcin/11.8.1249
DO - 10.1093/carcin/11.8.1249
M3 - Article
C2 - 2387010
AN - SCOPUS:0025072310
VL - 11
SP - 1249
EP - 1254
JO - Carcinogenesis
JF - Carcinogenesis
SN - 0143-3334
IS - 8
ER -