Fail P A, Anderson S A, Friedman M A
Research Triangle Institute, Research Triangle Park, North Carolina 27709-2194, USA.
Toxicol Sci. 1999 Nov;52(1):107-21. doi: 10.1093/toxsci/52.1.107.
Modulation of endocrine function is frequently a confounding factor in the interpretation of chronic rodent toxicology studies. Of particular interest are agents that cause deviation of thyroid hormone homeostasis and result in thyroid cancer for rodents. An endocrine challenge test (ECT), commonly used to study endocrine organ health in human and veterinary medicine, quantifies the response of the thyroid to tropic hormones. This study compared the response of Fischer (F344) and Sprague-Dawley (SD) rats to a thyrotropin-releasing hormone (TRH) ECT and a thyroid-stimulating hormone (TSH) ECT and characterized the dose-response curve. TSH, thyroxine (T4), triiodothyronine (T3), and prolactin responses were characterized for several doses of TRH over a 4-h time period. Animals were equipped with intra-atrial cannulae and were free moving at all times during blood sampling. Both strains of rats responded to intravenous TRH by releasing TSH into their blood in a dose-responsive fashion. At doses of > or = 100 ng, TSH concentrations were increased by more than 2-fold at 2 min. Concentrations reached a maximum at 15 min for doses of 100 ng/100 g body weight (bw) to 5000 ng/100g bw. The effective dose 50 (ED50) of TRH (that dose causing release of half maximal TSH concentrations) was 61 ng in F344 rats and 78 ng in SD rats. The ED75 was 173 ng and 217 ng/100 g bw, respectively. The response of T4 and T3 after TRH ECT and TSH ECT was highly variable. F344 rats responded with an increase in levels of both hormones, starting at 60 min and continuing through 240 min. In SD rats, the presence of a thyroid hormone response (T4) was present, although that of T3 was not clear. These data provide essential information for design of toxicology studies focused on the effects of toxicants and drugs on the pituitary-thyroid axis.
内分泌功能的调节常常是慢性啮齿动物毒理学研究解读中的一个混杂因素。特别令人感兴趣的是那些导致甲状腺激素稳态偏离并致使啮齿动物患甲状腺癌的物质。一种内分泌激发试验(ECT),常用于人类和兽医学中研究内分泌器官健康状况,它可量化甲状腺对促激素的反应。本研究比较了Fischer(F344)大鼠和Sprague-Dawley(SD)大鼠对促甲状腺激素释放激素(TRH)ECT及促甲状腺激素(TSH)ECT的反应,并对剂量-反应曲线进行了表征。在4小时时间段内,对几种剂量的TRH的TSH、甲状腺素(T4)、三碘甲状腺原氨酸(T3)和催乳素反应进行了表征。动物配备了心房插管,在采血过程中始终可自由活动。两种品系的大鼠对静脉注射的TRH均以剂量反应方式将TSH释放到血液中。在剂量≥100 ng时,2分钟时TSH浓度增加超过2倍。对于100 ng/100 g体重(bw)至5000 ng/100 g bw的剂量,浓度在15分钟时达到最大值。TRH的半数有效剂量(ED50)(即引起TSH浓度释放至最大值一半的剂量)在F344大鼠中为61 ng,在SD大鼠中为78 ng。ED75分别为173 ng和217 ng/100 g bw。TRH ECT和TSH ECT后T4和T3的反应高度可变。F344大鼠两种激素水平均升高,从60分钟开始并持续至240分钟。在SD大鼠中,存在甲状腺激素反应(T4),但T3的反应不明确。这些数据为设计关注毒物和药物对垂体-甲状腺轴影响的毒理学研究提供了重要信息。