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丙硫氧嘧啶和甲巯咪唑在甲状腺过氧化物酶催化的甲状腺球蛋白碘化反应中对甲状腺素和3,5,3'-三碘甲状腺原氨酸形成的优先抑制作用。

Preferential inhibition of thyroxine and 3,5,3'-triiodothyronine formation by propylthiouracil and methylmercaptoimidazole in thyroid peroxidase-catalyzed iodination of thyroglobulin.

作者信息

Engler H, Taurog A, Dorris M L

出版信息

Endocrinology. 1982 Jan;110(1):190-7. doi: 10.1210/endo-110-1-190.

Abstract

The present study was undertaken to determine whether the thioureylene antithyroid drugs propylthiouracil [6-propyl-2-thiouracil (PTU)] and methylmercaptoimidazole [1-methyl-2-mercaptoimidazole (MMI)] have a specific inhibitory effect on the thyroid peroxidase (TPO)-catalyzed conversion of diiodotyrosine to T4 (coupling reaction) independent of their well known inhibitory effect on peroxidase-catalyzed iodination. We have employed model incubation systems containing highly purified TPO to examine this question. Most experiments were performed with a model iodination system containing TPO, low iodine thyroglobulin, [131]iodide, and glucose-glucose oxidase. Both PTU and MMI are effective inhibitors of iodination of this system at physiological concentrations, and the system is well suited for studying the simultaneous action of these drugs on iodination and coupling. The addition of graded doses of the drugs to the iodination system demonstrated a relatively greater inhibitory effect on iodothyronine than on iodotyrosine formation. However, this observation in itself does not establish a specific inhibitory effect on coupling, since the formation of T4 involves a reaction between two molecules of 3,5-diiodotyrosine (DIT). The rate of this reaction, therefore, is second order with respect to DIT concentration, and the inhibition of DIT formation by thioureylene drugs would be expected to result in a disproportionately greater reduction in T4 formation even id there were no selective inhibitory effect of the drugs on the coupling reaction. Under certain conditions of incubation, however, it was possible to demonstrate a significant inhibitory effect on T4 and T3 formation without any decrease (in fact, a slight increase) in diiodotyrosine formation. These observations indicate that, at least under some conditions, PTU and MMI can exert a specific inhibitory effect on the coupling reaction. In the case of PTU, a specific inhibitory effect on coupling was also demonstrated with an incubation system in which TPO-catalyzed coupling was measured in the absence of iodination.

摘要

本研究旨在确定硫脲类抗甲状腺药物丙硫氧嘧啶[6-丙基-2-硫氧嘧啶(PTU)]和甲巯咪唑[1-甲基-2-巯基咪唑(MMI)]是否对甲状腺过氧化物酶(TPO)催化的二碘酪氨酸转化为T4的反应(偶联反应)具有特异性抑制作用,而不依赖于它们对过氧化物酶催化碘化反应的众所周知的抑制作用。我们采用了含有高度纯化TPO的模型孵育系统来研究这个问题。大多数实验是在一个含有TPO、低碘甲状腺球蛋白、[131]碘化物和葡萄糖-葡萄糖氧化酶的模型碘化系统中进行的。PTU和MMI在生理浓度下都是该系统碘化反应的有效抑制剂,并且该系统非常适合研究这些药物对碘化和偶联反应的同时作用。向碘化系统中添加分级剂量的药物显示,对碘甲状腺原氨酸的抑制作用比对碘酪氨酸形成的抑制作用相对更大。然而,这一观察结果本身并不能确定对偶联反应有特异性抑制作用,因为T4的形成涉及两分子3,5-二碘酪氨酸(DIT)之间的反应。因此,该反应的速率相对于DIT浓度是二级反应,并且即使药物对偶联反应没有选择性抑制作用,硫脲类药物对DIT形成的抑制作用也预计会导致T4形成的减少比例更大。然而,在某些孵育条件下,可以证明对T4和T3形成有显著抑制作用,而二碘酪氨酸的形成没有任何减少(实际上,有轻微增加)。这些观察结果表明,至少在某些条件下,PTU和MMI可以对偶联反应发挥特异性抑制作用。就PTU而言,在一个不进行碘化反应而测量TPO催化偶联反应的孵育系统中,也证明了对偶联反应有特异性抑制作用。

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