Stoker T E, Ferrell J M, Laws S C, Cooper R L, Buckalew A
Endocrinology Branch, Reproductive Toxicology Division, NHEERL, Office of Research and Development, United States Environmental Protection Agency, Research Triangle Park, NC 27711, USA.
Toxicology. 2006 Nov 10;228(1):58-65. doi: 10.1016/j.tox.2006.08.026. Epub 2006 Aug 26.
The U.S. EPA Endocrine Disruptor Screening Program (EDSP) Tier 1 male pubertal protocol was designed as a screen to detect endocrine-disrupting chemicals which may alter reproductive development or thyroid function. One purpose of this in vivo screening protocol is to detect thyrotoxicants via a number of different mechanisms of action, such as thyroid hormone synthesis or clearance. Here we evaluate the ability of this EDSP male pubertal protocol to detect the known thyrotoxicant ammonium perchlorate as an endocrine disruptor. Ammonium perchlorate is a primary ingredient in rocket fuel, fertilizers, paints, and lubricants. Over the past 50 years, potassium perchlorate has been used to treat hyperthyroidism in humans. Perchlorate alters thyroid hormone secretion by competitively inhibiting iodide uptake by the thyroid gland. In this study, ammonium perchlorate was administered at 62.5, 125, 250, and 500 mg/kg to male Wistar rats based on a pilot study of oral dosing. Doses of 125-500 mg/kg perchlorate decreased T4 in a dose-dependent manner. TSH was significantly increased in a dose-responsive manner at the same doses, while T3 was unchanged at any dose. Thyroid histology was significantly altered at all doses, even at the 62.5 mg/kg, with a clear dose-dependent decrease in colloid area and increase in follicular cell height. No effects on preputial separation, a marker of pubertal progression, or reproductive tract development were observed at any dose. These results demonstrate that the male pubertal protocol is useful for detecting thyrotoxicants which target the thyroid axis by this mechanism (altered uptake of iodide). This study also found that perchlorate exposure during this period did not alter any of the reproductive developmental endpoints.
美国环境保护局(EPA)的内分泌干扰物筛选计划(EDSP)一级雄性青春期试验方案旨在作为一种筛选手段,以检测可能改变生殖发育或甲状腺功能的内分泌干扰化学物质。这个体内筛选试验方案的一个目的是通过多种不同的作用机制,如甲状腺激素合成或清除,来检测甲状腺毒剂。在此,我们评估该EDSP雄性青春期试验方案检测已知甲状腺毒剂高氯酸铵作为内分泌干扰物的能力。高氯酸铵是火箭燃料、肥料、油漆和润滑剂中的主要成分。在过去50年里,高氯酸钾一直被用于治疗人类的甲状腺功能亢进症。高氯酸盐通过竞争性抑制甲状腺对碘的摄取来改变甲状腺激素的分泌。在本研究中,根据口服给药的初步研究,以62.5、125、250和500mg/kg的剂量给雄性Wistar大鼠施用高氯酸铵。125 - 500mg/kg的高氯酸盐剂量以剂量依赖性方式降低T4。在相同剂量下,促甲状腺激素(TSH)以剂量反应性方式显著增加,而T3在任何剂量下均无变化。所有剂量下甲状腺组织学均有显著改变,即使在62.5mg/kg时也是如此,胶体区域明显呈剂量依赖性减少,滤泡细胞高度增加。在任何剂量下均未观察到对青春期进展标志物包皮分离或生殖道发育的影响。这些结果表明,雄性青春期试验方案对于检测通过这种机制(碘摄取改变)靶向甲状腺轴的甲状腺毒剂是有用的。本研究还发现,在此期间接触高氯酸盐并未改变任何生殖发育终点。