Cross species extrapolation of the disruption of thyroid hormone synthesis by oxyfluorfen using in vitro data, physiologically based pharmacokinetic (PBPK), and thyroid hormone kinetics models

IF 2.9 Q2 TOXICOLOGY
Rhylee Decrane , Tammy Stoker , Ashley Murr , Jermaine Ford , Hisham El-Masri
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Abstract

The thyroid hormones play key roles in physiological processes such as regulation of the metabolic and cardiac systems as well as the development of the brain and surrounding sympathetic nervous system. Recent efforts to screen environmental chemicals for their ability to alter thyroid hormone synthesis, transport, metabolism and/or function have identified novel chemicals that target key processes in the thyroid pathway. One newly identified chemical, oxyfluorfen, is a diphenyl-ether herbicide used for control of annual broadleaf and grassy weeds in a variety of tree fruit, nut, vine, and field crops. Using in vitro high-throughput screening (HTS) assays, oxyfluorofen was identified to be a potent inhibitor of the thyroidal sodium-iodide symporter (NIS). To quantitatively assess this inhibition mechanism in vivo, we extrapolated in vitro NIS inhibition data to in vivo disruption of thyroid hormones synthesis in rats using physiologically based pharmacokinetic (PBPK) and thyroid hormone kinetics models. The overall computational model (chemical PBPK and THs kinetic sub-models) was calibrated against in vivo data for the levels of oxyfluorfen in thyroid tissue and serum and against serum levels of thyroid hormones triiodothyronine (T3) and thyroxine (T4) in rats. The rat thyroid model was then extrapolated to humans using human in vitro HTS data for NIS inhibition and the chemical specific hepatic clearance rate in humans. The overall species extrapolated PBPK-thyroid kinetics model can be used to predict dose–response (% drop in thyroid serum levels compared to homeostasis) relationships in humans. These relationships can be used to estimate points of departure for health risks related to a drop in serum levels of TH hormones based on HTS assays in vitro to in vivo extrapolation (IVIVE), toxicokinetics, and physiological principles.

Abstract Image

利用体外数据、基于生理的药代动力学(PBPK)和甲状腺激素动力学模型,对氟氧芬对甲状腺激素合成的破坏进行跨物种外推
甲状腺激素在生理过程中发挥关键作用,如代谢和心脏系统的调节,以及大脑和周围交感神经系统的发育。最近对环境化学物质改变甲状腺激素合成、转运、代谢和/或功能能力的研究发现了针对甲状腺通路关键过程的新化学物质。一种新发现的化学物质氟氧芬是一种二苯醚除草剂,用于控制各种果树、坚果、藤本植物和大田作物中的一年生阔叶杂草和草类杂草。使用体外高通量筛选(HTS)测定,氟氧芬被鉴定为甲状腺碘化钠同体(NIS)的有效抑制剂。为了定量评估这种体内抑制机制,我们使用基于生理的药代动力学(PBPK)和甲状腺激素动力学模型,将体外NIS抑制数据外推到大鼠体内甲状腺激素合成的破坏。总体计算模型(化学PBPK和THs动力学子模型)根据大鼠体内甲状腺组织和血清中氟氧芬水平以及血清中甲状腺激素三碘甲状腺原氨酸(T3)和甲状腺素(T4)水平的数据进行校准。然后利用人体外HTS数据将大鼠甲状腺模型外推到人身上,以研究NIS的抑制作用和人体内化学物质特异性肝脏清除率。整体物种外推pbpk -甲状腺动力学模型可用于预测人类的剂量-反应(与体内平衡相比甲状腺血清水平下降%)关系。基于体外体内外推法(IVIVE)、毒物动力学和生理原理的HTS测定,这些关系可用于估计与血清促甲状腺激素水平下降相关的健康风险起点。
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来源期刊
Current Research in Toxicology
Current Research in Toxicology Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
4.70
自引率
3.00%
发文量
33
审稿时长
82 days
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