LoPresti J S, Eigen A, Kaptein E, Anderson K P, Spencer C A, Nicoloff J T
Department of Medicine, University of Southern California, School of Medicine, Los Angeles 90033.
J Clin Invest. 1989 Nov;84(5):1650-6. doi: 10.1172/JCI114343.
To elucidate the mechanisms involved in altering serum 3,3',5'-triiodothyronine (rT3) levels with absolute or relative low 3,5,3'-triiodothyronine (T3) states in man, agents capable of lowering circulating T3 levels were sequentially administered to six euthyroid subjects. These agents included propylthiouracil (PTU) (300 mg/6 h X 5 d), dexamethasone (DEX) (2 mg/6 h X 5 d), and thyroxine (T4) (3.0 mg load and 0.3 mg/d X 5 d). [125I] rT3 clearance rates and rT3 production rates were then determined. Increased serum rT3 levels and rT3/T4 values occurred with both PTU and DEX as compared with control, while T4 increased serum rT3 but did so without changing rT3/T4 values. The rT3 clearance rate was significantly decreased by PTU without altering production rate, while DEX increased the rT3 production rate without altering the rT3 clearance rate. T4 administration did not change rT3 clearance but proportionately increased rT3 production. These responses indicate that circulating rT3 predominantly originates from a non-PTU inhibitable deiodinase enzyme system located in extrahepatic tissues. This enzyme system appears to have a high capacity and low affinity for T4 and can be stimulated by DEX administration.
为阐明在人体处于绝对或相对低三碘甲状腺原氨酸(T3)状态时血清反三碘甲状腺原氨酸(rT3)水平改变所涉及的机制,对6名甲状腺功能正常的受试者依次给予能够降低循环T3水平的药物。这些药物包括丙硫氧嘧啶(PTU)(300毫克/6小时×5天)、地塞米松(DEX)(2毫克/6小时×5天)和甲状腺素(T4)(负荷量3.0毫克及0.3毫克/天×5天)。然后测定[125I]rT3清除率和rT3生成率。与对照组相比,PTU和DEX均使血清rT3水平及rT3/T4值升高,而T4使血清rT3升高,但未改变rT3/T4值。PTU显著降低rT3清除率而不改变生成率,而DEX增加rT3生成率而不改变rT3清除率。给予T4未改变rT3清除率,但按比例增加rT3生成。这些反应表明,循环rT3主要源自位于肝外组织的一种不受PTU抑制的脱碘酶系统。该酶系统似乎对T4具有高容量和低亲和力,且可通过给予DEX而被刺激。