Effects of pethoxamid treatment on the disposition of thyroxine in rats

IF 3.3 3区 医学 Q2 PHARMACOLOGY & PHARMACY Toxicology and applied pharmacology Pub Date : 2024-05-09 DOI:10.1016/j.taap.2024.116959
Appavu Chandrasekaran , Karin Bentley , Robert McClanahan , Gopinath Nallani
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Abstract

Pethoxamid (PXA) is a chloroacetamide herbicide that works by inhibiting the germination of target weeds in crops. PXA is not a genotoxic agent, however, in a two-year chronic toxicity study, incidence of thyroid follicular cell hyperplasia was observed in male rats treated at a high dose. Many non-mutagenic chemicals, including agrochemicals are known to produce thyroid hyperplasia in rodents through a hepatic metabolizing enzyme induction mode of action (MoA). In this study, the effects of oral gavage PXA treatment at 300 mg/kg for 7 days on the disposition of intravenously (iv) administered radio-labeled thyroxine ([125I]-T4) was assessed in bile-duct cannulated (BDC) rats. Another group of animals were treated with phenobarbital (PB, 100 mg/kg), a known enzyme inducer, serving as a positive control. The results showed significant increase (p < 0.01) in the mean liver weights in the PB and PXA-treated groups relative to the control group. The serum total T4 radioactivity Cmax and AUC04 values for PB and PXA-treated groups were lower than for the control group, suggesting increased clearance from serum. The mean percentages of administered radioactivity excreted in bile were 7.96 ± 0.38%, 16.13 ± 5.46%, and 11.99 ± 2.80% for the control, PB and PXA groups, respectively, indicating increased clearance via the bile in the treated animals. These data indicate that PXA can perturb the thyroid hormone homeostasis in rats by increasing T4 elimination in bile, possibly through enzyme induction mechanism similar to PB. In contrast to humans, the lack of high affinity thyroid binding globulin (TBG) in rats perhaps results in enhanced metabolism of T4 by uridine diphosphate glucuronosyl transferase (UGT). Since this liver enzyme induction MoA for thyroid hyperplasia by PB is known to be rodent specific, PXA effects on thyroid can also be considered not relevant to humans. The data from this study also suggest that incorporating a BDC rat model to determine thyroid hormone disposition using [125I]-T4 is valuable in a thyroid mode of action analysis.

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乙草胺处理对大鼠甲状腺素处置的影响
Pethoxamid(PXA)是一种氯乙酰胺类除草剂,通过抑制作物中目标杂草的发芽而发挥作用。PXA 不具有基因毒性,但在一项为期两年的慢性毒性研究中,观察到高剂量处理的雄性大鼠出现甲状腺滤泡细胞增生。已知包括农用化学品在内的许多非致突变化学品会通过肝脏代谢酶诱导作用模式(MoA)在啮齿动物体内产生甲状腺增生。本研究评估了在胆管插管(BDC)大鼠中连续 7 天口服 300 毫克/千克 PXA 对静脉注射放射性标记甲状腺素([125I]-T4)的影响。另一组动物用已知的酶诱导剂苯巴比妥(PB,100 毫克/千克)作为阳性对照。结果表明,苯巴比妥和 PXA 处理组的血清清除率明显增加(p max 和 AUC0-4 值均低于对照组),表明血清清除率增加。对照组、PB 组和 PXA 组通过胆汁排泄的放射性平均百分比分别为 7.96 ± 0.38%、16.13 ± 5.46% 和 11.99 ± 2.80%,表明治疗动物通过胆汁的清除率增加。这些数据表明,PXA 可通过增加 T4 在胆汁中的排出量来扰乱大鼠的甲状腺激素平衡,可能是通过与 PB 相似的酶诱导机制。与人类不同的是,大鼠体内缺乏高亲和力的甲状腺结合球蛋白(TBG),这可能会导致二磷酸尿苷葡萄糖醛酸转移酶(UGT)对 T4 的代谢增强。众所周知,PB 诱导甲状腺增生的这种肝酶诱导作用是啮齿动物特有的,因此也可以认为 PXA 对甲状腺的影响与人类无关。本研究的数据还表明,使用[125I]-T4 结合 BDC 大鼠模型来确定甲状腺激素的处置对于甲状腺作用模式分析很有价值。
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来源期刊
CiteScore
6.80
自引率
2.60%
发文量
309
审稿时长
32 days
期刊介绍: Toxicology and Applied Pharmacology publishes original scientific research of relevance to animals or humans pertaining to the action of chemicals, drugs, or chemically-defined natural products. Regular articles address mechanistic approaches to physiological, pharmacologic, biochemical, cellular, or molecular understanding of toxicologic/pathologic lesions and to methods used to describe these responses. Safety Science articles address outstanding state-of-the-art preclinical and human translational characterization of drug and chemical safety employing cutting-edge science. Highly significant Regulatory Safety Science articles will also be considered in this category. Papers concerned with alternatives to the use of experimental animals are encouraged. Short articles report on high impact studies of broad interest to readers of TAAP that would benefit from rapid publication. These articles should contain no more than a combined total of four figures and tables. Authors should include in their cover letter the justification for consideration of their manuscript as a short article.
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