Pascual A, Obregon M J, de Escobar G M
Endocrinology. 1979 Jun;104(6):1574-9. doi: 10.1210/endo-104-6-1574.
We have studied the effects of alpha-methyl-p-tyrosine (alpha-MPT), an inhibitor of tyrosine hydroxylase, on the in vivo conversion of L-T4 (T4) to 3',3,5-triiodo-L-thyronine (T3), and on the biological effectiveness of T4. Thyroidectomized rats were used and were injected daily with T4 maintenance doses. Three different types of experiments were carred out. The first involved isotopic equilibration with 125I-labeled T4 and measurement of urinary 125I excretion. The second series involved the injection of a single dose of [125I]T4, with the amounts of [125I]T3 in different tissues being studied 7 or 20 h later. The third series involved daily treatment for 13 days with T4 and alpha-MPT, at the end of ehich the liver alpha-glycerophosphate dehydrogenase activity was measured as a parameter of the biological effects of the hormone. Though the experimental approaches used clearly disclosed the well known effects of 6-propyl-2-thiouracil, no clear-cut effects of alpha-MPT were observed. It is concluded that alpha-MPT neither inhibits the conversion of T4 to T3 in vivo in rats nor affects the biological potency of a given dose of T4, at least to an extent compararble to that observed when 6-propyl-2-thiouracil is used. Thus, present results do not support the hypothesis that tyrosine hydroxylase is involved in the extrathyroidal deiodination of T4 to T3.
我们研究了酪氨酸羟化酶抑制剂α-甲基-对-酪氨酸(α-MPT)对L-甲状腺素(T4)在体内转化为3',3,5-三碘-L-甲状腺原氨酸(T3)的影响,以及对T4生物学效应的影响。使用了甲状腺切除的大鼠,并每天注射维持剂量的T4。进行了三种不同类型的实验。第一个实验涉及用125I标记的T4进行同位素平衡,并测量尿中125I的排泄量。第二个系列实验涉及注射单剂量的[125I]T4,7或20小时后研究不同组织中[125I]T3的含量。第三个系列实验涉及用T4和α-MPT每天治疗13天,在实验结束时测量肝脏α-甘油磷酸脱氢酶活性,作为该激素生物学效应的一个参数。尽管所采用的实验方法清楚地揭示了6-丙基-2-硫脲的众所周知的效应,但未观察到α-MPT有明确的效应。得出的结论是,α-MPT既不抑制大鼠体内T4向T3的转化,也不影响给定剂量T4的生物学效能,至少在与使用6-丙基-2-硫脲时观察到的程度相当的范围内是如此。因此,目前的结果不支持酪氨酸羟化酶参与T4在甲状腺外脱碘生成T3这一假说。