Prenatal test cohort of a modified rat comparative thyroid assay adding brain thyroid hormone measurements and histology but lowering group size appears able to detect disruption by sodium phenobarbital

IF 2.9 Q2 TOXICOLOGY Current Research in Toxicology Pub Date : 2024-01-01 DOI:10.1016/j.crtox.2024.100168
Kenta Minami , Akira Sato , Naruto Tomiyama , Keiko Ogata , Tadashi Kosaka , Hitoshi Hojo , Naofumi Takahashi , Hidenori Suto , Hiroaki Aoyama , Tomoya Yamada
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Abstract

The Comparative Thyroid Assay (CTA, USEPA) is a screening test for thyroid hormone (TH) disruption in peripheral blood of dams and offspring. Recently, we began investigating feasible improvements to the CTA by adding examination of offspring brain TH concentrations and brain histopathology. In addition, we hypothesize that the number of animals required could be reduced by 50 % while still maintaining sensitivity to characterize treatment related changes in THs. Previously, we showed that the prenatal test cohort of the modified CTA could detect 1000 ppm sodium phenobarbital (NaPB)-induced suppression of brain T3 (by 9 %) and T4 (by 33 %) with no significant changes in serum T3 and T4 (less than 8 %). In the current study we expanded the dose response in a prenatal test cohort. Pregnant SD rats (N = 10/group) were exposed to 0, 1000 or 1500 ppm NaPB in the diet from gestational days (GD) 6 to GD20. Serum THs concentrations in GD20 dams together with serum/brain THs concentrations and brain histopathology in the GD20 fetuses were examined. NaPB dose-dependently suppressed serum T3 (up to −26 %) and T4 (up to −44 %) in dams, with suppression of T3 in serum (up to −26 %) and brain (up to −18 %) and T4 in serum (up to −26 %) and brain (up to −29 %) of fetuses but without clear dose dependency. There were no remarkable findings that deviated significantly from controls in GD20 fetal brain by qualitative histopathology. Overall, the present study suggests that the prenatal test cohort of this modified CTA is able to detect the expected fetal TH disruptions by prenatal exposure to NaPB, while also reducing the number of animals used by 50 %, consistent with the results of our previous study. These findings add to the suggestion that lowering group sizes and adding endpoints may be a useful alternative to the original CTA design.

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改良的大鼠甲状腺比较试验的产前试验队列增加了脑甲状腺激素测量和组织学研究,但降低了试验组的规模,似乎能够检测出苯巴比妥钠的干扰作用
比较甲状腺测定法(CTA,USEPA)是一种筛查母体和子代外周血中甲状腺激素(TH)紊乱的检测方法。最近,我们开始研究改进 CTA 的可行性,增加了对后代脑中 TH 浓度和脑组织病理学的检查。此外,我们假设所需的动物数量可以减少 50%,同时仍能保持对与治疗相关的 THs 变化特征的敏感性。此前,我们曾研究表明,改良 CTA 的产前试验队列可检测到 1000 ppm 苯巴比妥钠(NaPB)诱导的脑 T3(降低 9%)和 T4(降低 33%)抑制,而血清 T3 和 T4 无明显变化(低于 8%)。在本研究中,我们扩大了产前试验队列中的剂量反应。怀孕的 SD 大鼠(N = 10/组)在妊娠期(GD)6 至 GD20 的饮食中分别摄入 0、1000 或 1500 ppm 的 NaPB。对 GD20 母鼠的血清 THs 浓度以及 GD20 胎儿的血清/脑 THs 浓度和脑组织病理学进行了检测。NaPB剂量依赖性地抑制了母体血清中的T3(高达-26%)和T4(高达-44%),抑制了胎儿血清中的T3(高达-26%)和脑中的T3(高达-18%)以及血清中的T4(高达-26%)和脑中的T4(高达-29%),但没有明显的剂量依赖性。通过定性组织病理学检查,在 GD20 胎儿大脑中没有明显偏离对照组的发现。总之,本研究表明,这种改良 CTA 的产前检测队列能够检测出产前暴露于 NaPB 对胎儿 TH 的预期干扰,同时还能将使用的动物数量减少 50%,这与我们之前的研究结果一致。这些研究结果进一步表明,降低实验组规模并增加终点可能是原始 CTA 设计的有效替代方案。
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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
期刊最新文献
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