Balsam A, Sexton F, Ingbar S H
Endocrinology. 1981 Feb;108(2):472-7. doi: 10.1210/endo-108-2-472.
In the present studies, we have evaluated the effects of fasting, variations in thyroid state, and interactions thereof on the kinetic properties of the microsomal enzyme in rat liver that generates T3 from T4. The formation of T3 and T4 (T3-neogenesis) in preparations of rat liver microsomes enriched with 10 mM dithiothreitol was monitored by assessing the formation of [125I]T3 from [125I]T4 in the presence of various concentrations of stable T4. T3-neogenesis in this system was a saturable process that obeyed the laws of first order enzyme kinetics. The effects of diverse in vivo manipulations on the kinetics of T3-neogenesis were assessed. The Vmax was markedly decreased in preparations from thyroidectomized animals, being, respectively, partially and completely restored to normal with daily maintenance therapy with T4, (0.5 and 1.5 microgram/100 g BW) and markedly increased after the administration of supraphysiological replacement doses of T4 (5.0 microgram/100 g . day). Km was not affected by alterations in thyroid state. In experiments concerning the effects of fasting, cognizance was taken of the fact that hypothyroidism regularly evolves as a consequence of fasting. The Vmax was decreased markedly, and Km was slightly decreased in preparations from intact rats fasted 72 h but not given physiological replacement with T4 or T3. In contrast, Vmax and Km were unchanged in hepatic microsomes from intact rats fasted 72 h but given daily parenteral replacement with T4 (1.5 microgram/100 g) or T3 (0.5 microgram/100 g). These data demonstrate that hypothyroidism resulting from either thyroidectomy or fasting produces decreased intrinsic activity of the microsomal T4 5'-monodeiodinase. In contrast, fasting without concurrent hypothyroidism does not influence the intrinsic activity of the hepatic T3-neogenetic enzyme. (Endocrinology 108: 472, 1981)
在本研究中,我们评估了禁食、甲状腺状态变化及其相互作用对大鼠肝脏微粒体酶(该酶可将T4转化为T3)动力学特性的影响。在富含10 mM二硫苏糖醇的大鼠肝脏微粒体制剂中,通过在各种稳定T4浓度存在的情况下评估[125I]T3从[125I]T4的生成情况,来监测T3和T4(T3新生)的形成。该系统中的T3新生是一个遵循一级酶动力学规律的可饱和过程。评估了多种体内操作对T3新生动力学的影响。甲状腺切除动物的制剂中Vmax显著降低,分别用T4(0.5和1.5微克/100克体重)进行每日维持治疗后,部分和完全恢复正常,而给予超生理替代剂量的T4(5.0微克/100克·天)后显著增加。Km不受甲状腺状态改变的影响。在关于禁食影响的实验中,考虑到甲状腺功能减退通常是禁食的结果。禁食72小时但未给予T4或T3生理替代的完整大鼠的制剂中,Vmax显著降低,Km略有降低。相反,禁食72小时但每日经肠胃外给予T4(1.5微克/100克)或T3(0.5微克/100克)的完整大鼠肝脏微粒体中,Vmax和Km未发生变化。这些数据表明,甲状腺切除或禁食导致的甲状腺功能减退会使微粒体T4 5'-单脱碘酶的内在活性降低。相反,无并发甲状腺功能减退的禁食不影响肝脏T3新生酶的内在活性。(《内分泌学》108: 472, 1981)