甲状腺素在离体大鼠肾小管中生成三碘甲状腺原氨酸和逆转三碘甲状腺原氨酸。

P Heyma, R G Larkins, J R Stockigt, D G Campbell
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引用次数: 18

摘要

1. 利用胶原酶消化制备的离体肾小管,研究了完整细胞中甲状腺素转化为三碘甲状腺原氨酸和逆转三碘甲状腺原氨酸的过程。2. 甲状腺素转化为三碘甲状腺原氨酸和逆转三碘甲状腺原氨酸的逐渐增加至少持续90分钟。从增加甲状腺素量产生三碘甲状腺原氨酸的研究表明,甲状腺素到三碘甲状腺原氨酸的转化是饱和的。4. 碘和卡咪唑对甲状腺素向三碘甲状腺原氨酸的转化没有影响。5. 6-丙基-2-硫脲嘧啶对甲状腺素转化为三碘甲状腺原氨酸具有直接的非竞争性抑制作用,在体内治疗范围内,丙基硫脲嘧啶浓度可抑制75%的转化。丙硫氧嘧啶还能抑制相似浓度丙硫氧嘧啶下甲状腺素净生成反三碘甲状腺原氨酸,并抑制反三碘甲状腺原氨酸随后的降解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The formation of tri-iodothyronine and reverse tri-iodothyronine from thyroxine in isolated rat renal tubules.

1. Conversion of thyroxine into tri-iodothyronine and reverse tri-iodothyronine in intact cells was studied with isolated renal tubules prepared by collagenase digestion. 2. Conversion of thyroxine into tri-iodothyronine and reverse tri-iodothyronine increased progressively for at least 90 min. 3. Studies of tri-iodothyronine production from increasing amounts of thyroxine revealed that the thyroxine to tri-iodothyronine conversion is saturable. 4. Iodine and carbimazole had no effect on the thyroxine to tri-iodothyronine conversion. 5. 6-Propyl-2-thiouracil had a direct non-competitive inhibitory effect on the conversion of thyroxine into tri-iodothyronine with a 75% inhibition of the conversion at a propylthiouracil concentration within the therapeutic range in vivo. Propylthiouracil also inhibited the net formation of reverse tri-iodothyronine from thyroxine at a similar propylthiouracil concentration, as well as inhibiting the subsequent degradation of reverse tri-iodothyronine.

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