Laurberg P
Horm Metab Res. 1982 Jan;14(1):46-9. doi: 10.1055/s-2007-1018916.
A radioimmunoassay for 3,5-diiodothyronine (3,5-T2) was developed using inner ring labeled 125l-3,5-T2 and a 3,5-T2 antibody produced in rabbits by immunization with 3,5-T2 coupled to human albumin. Separation of free and bound 3,5-T2 was achieved by ascending ion-exchange wick-chromatography. The detection limit was 4 pmol/l. The only important cross-reaction was with T3. It amounted to 0.11 % (mol/mol) and contributed only little to the 3,5-T2 measured in thyroid hydrolysate and thyroid effluent. It was ascertained that no significant loss or generation of 3,5-T2 took place during storage of thyroid effluent samples and during hydrolysis of thyroid homogenate. In four experiments employing eight thyroid lobes, 3,5-T2 was measured in hydrolysate and effluent from perfused dog thyroid lobes during single passage perfusion with a synthetic hormone free medium. During perfusion with control medium 3,5-T2 in effluent was stable around 40 pmol/l. Infusion of 100 microunits/ml TSH induced after a latency period of approximately 20 min a gradual increase in 3,5-T2 release to a level of approximately 180 pmol/l. 3,5-T2 in thyroid hydrolysate was 1.47 +/- 0.05 pmol/mg thyroid wet weight (mean +/- SD). There did not seem to be any major generation of 3,5-T2 by intrathyroidal iodothyronine deiodination. Thus thyroidal secretion of 3,5-T2 is very low and would probably not contribute significantly to the amounts of circulating 3,5-T2.
利用内环标记的125I-3,5-二碘甲状腺原氨酸(3,5-T2)和用与人类白蛋白偶联的3,5-T2免疫家兔产生的3,5-T2抗体,开发了一种3,5-T2的放射免疫分析方法。通过上升离子交换芯色谱法实现游离和结合的3,5-T2的分离。检测限为4 pmol/l。唯一重要的交叉反应是与T3的反应。其交叉反应率为0.11%(摩尔/摩尔),对甲状腺水解物和甲状腺流出物中测得的3,5-T2贡献很小。已确定在甲状腺流出物样品储存期间和甲状腺匀浆水解期间,3,5-T2没有明显损失或生成。在四个实验中,使用了八个甲状腺叶,在用不含合成激素的培养基单次灌注期间,测量了灌注的犬甲状腺叶水解物和流出物中的3,5-T2。在用对照培养基灌注期间,流出物中的3,5-T2稳定在约40 pmol/l左右。输注100微单位/ml促甲状腺激素(TSH)后,在大约20分钟的潜伏期后,3,5-T2释放逐渐增加至约180 pmol/l的水平。甲状腺水解物中的3,5-T2为1.47±0.05 pmol/mg甲状腺湿重(平均值±标准差)。甲状腺内碘甲状腺原氨酸脱碘似乎没有产生大量的3,5-T2。因此,3,5-T2的甲状腺分泌非常低,可能对循环中的3,5-T2量没有显著贡献。