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Toxicol Appl Pharmacol ; 180(1): 11-21, 2002 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-11922773

RESUMO

This study used an MCF-7 cell based ER-alpha reporter gene assay to assess chemical interactions within the following ternary mixtures: (1) three synthetic pesticides, methoxychlor (MXC), o,p-DDT, and dieldrin; (2) three polyaromatic hydrocarbons, benzo[a]pyrene (BAP), 1,2-benzanthracene (BENZ), and chrysene (CHRY); and (3) an endogenous estrogen, [17beta-estradiol, (E(2))]; a phytoestrogen, genistein (GEN); and a synthetic estrogen, o,p-DDT. A full factorial design in which four concentrations of each chemical were assessed in all possible combinations (64 treatment groups) was utilized. In addition, mixtures were tested in both a low range (concentrations near the individual chemical response thresholds) and a high range ( approximately 2-10x higher) experiment. A response surface was estimated using a nonlinear mixed model, and the cumulative response in each mixture was evaluated for departure from additivity. The mixture of E(2), GEN, and DDT exhibited antagonistic interactions (p < 0.001) in both concentration ranges. However, specific interactions between E(2)/GEN and E(2)/DDT differed between the low and high range concentrations. The BAP/BENZ/CHRY mixture did not depart significantly from additivity (p = 0.66) in either concentration range, although response levels were generally low. The MXC/DDT/dieldrin mixture did not depart significantly from additivity in either the high (p = 0.065), or low dose range (p = 0.506), with generally minimal responses dominated by MXC and DDT. This methodology has allowed for a rigorous statistical evaluation of potential departures from additive interactions in endocrine active mixtures. In no case was a significantly greater-than-additive (synergistic) interaction observed.


Assuntos
Receptores de Estrogênio/metabolismo , Xenobióticos/metabolismo , Bioensaio , Neoplasias da Mama/enzimologia , Neoplasias da Mama/genética , Simulação por Computador , Relação Dose-Resposta a Droga , Interações Medicamentosas , Receptor alfa de Estrogênio , Estrogênios/metabolismo , Estrogênios/farmacologia , Feminino , Regulação Enzimológica da Expressão Gênica/efeitos dos fármacos , Genes Reporter , Humanos , Luciferases/biossíntese , Luciferases/genética , Modelos Biológicos , Praguicidas/metabolismo , Praguicidas/farmacologia , Hidrocarbonetos Policíclicos Aromáticos/metabolismo , Hidrocarbonetos Policíclicos Aromáticos/farmacologia , Receptores de Estrogênio/genética , Transfecção , Células Tumorais Cultivadas , Xenobióticos/farmacologia , beta-Galactosidase/biossíntese , beta-Galactosidase/genética
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