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在分离的大鼠肾小管中由甲状腺素形成三碘甲状腺原氨酸和反式三碘甲状腺原氨酸。

The formation of tri-iodothyronine and reverse tri-iodothyronine from thyroxine in isolated rat renal tubules.

作者信息

Heyma P, Larkins R G, Stockigt J R, Campbell D G

出版信息

Clin Sci Mol Med Suppl. 1978 Dec;55(6):567-72. doi: 10.1042/cs0550567.

Abstract
  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.
摘要
  1. 采用胶原酶消化法制备的离体肾小管,研究了完整细胞中甲状腺素转化为三碘甲状腺原氨酸及反式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及反式三碘甲状腺原氨酸的过程至少持续90分钟且逐渐增加。3. 对不同量甲状腺素生成三碘甲状腺原氨酸的研究表明,甲状腺素向三碘甲状腺原氨酸的转化具有饱和性。4. 碘和卡比马唑对甲状腺素向三碘甲状腺原氨酸的转化无影响。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,在体内治疗范围内的丙基硫氧嘧啶浓度下,该转化受到75%的抑制。在相似的丙基硫氧嘧啶浓度下,丙基硫氧嘧啶还抑制了甲状腺素反式三碘甲状腺原氨酸的净生成,以及随后反式三碘甲状腺原氨酸的降解。

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