Integrating tissue dosimetry and mode of action to evaluate atrazine dose-response.

摘要

Atrazine (ATRA) is a widely used chlorotriazine herbicide that causes neuroendocrine effects in animal toxicity studies. While the mechanism by which ATRA alters neuroendocrine function is not known, previous studies indicated that ATRA had anti-estrogenic properties in vitro and in vivo. In addition, ATRA is metabolized to chlorinated metabolites by P450 mediated saturable to oxidative metabolism and to non-chlorinated metabolites by GST-mediated GSH conjugation. Knowledge of tissue dosimetry and mode of action is especially important for determining risk posed by ATRA exposure. The studies presented in this dissertation examined the anti-estrogenic mode of action of ATRA and DACT in brain and the processes that control the kinetic disposition of ATRA and its metabolites in plasma and target tissue (the brain) under conditions that cause LH surge suppression. A series of pharmacokinetic models were developed to describe in vitro and in vivo kinetic data on ATRA and its metabolites. The time-course concentrations of ATRA and the chlorinated metabolites in plasma and brain were regulated by dose-dependent and sequential absorption of compound from gut, oxidative metabolism in the liver and intestine, reactivity with hemoglobin in red blood cells and with plasma proteins, systemic clearance by GST mediated GSH conjugation and urinary elimination. DACT was the major chlorotriazine present in tissue, representing over 95% of total chlorotriazine area under the concentration curve after dosing with ATRA.; In evaluating the neuroendocrine mode of action of Cl-TRIs, we determined that ATRA and DACT suppress the LH surge by mechanisms other than altering binding of estrogen to its cognate receptors in the hypothalamus. Moreover, pituitary responsiveness was altered in animals treated with concentrations of DACT that suppressed the estradiol/progesterone induced LH surge. The high degree of reactivity of DACT with sulfhydryl residues in rat hemoglobin indicate that tissue reactivity of DACT should be considered as a possible mode of action rather than direct interaction, either inhibition or activation, with cellular receptor molecules.; These present studies have improved our understanding of the mechanisms by which chlorotriazines alter the LH surge and the factors that control chlorotriazine tissue dose under conditions where neuroendocrine responses are observed.