Comparison of the effect of amiodarone and benziodarone on thyroxine metabolism and surface ECG.

Endocrinologia experimentalis Pub Date : 1989-12-01
S D Moulopoulos, D A Koutras, S Stamatelopoulos, A Souvatzoglou, G D Piperingos, G Philippou
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Abstract

This study examined whether or not the electrophysiological effect of amiodarone on the heart is mediated through its action on thyroxine metabolism. Serum thyroid hormones and ECG were evaluated before and serially during amiodarone (15 subjects) and benziodarone (15 subjects) administration. Both amiodarone and benziodarone shifted the peripheral conversion of thyroxine (P less than 0.001 for amiodarone and P less than 0.001 for benziodarone) towards reverse triiodothyronine and away from triiodothyronine, whilst TSH levels initially fell and then rose with both drugs. After amiodarone the heart rate decreased (P less than 0.025), whilst the PR (P less than 0.005) and the QT interval (P less than 0.005) corrected for the heart rate increased. By contrast with benziodarone only the PR interval decreased (P less than 0.05). Since both drugs had roughly similar effects on thyroid hormone metabolism but different ones on the ECG, our results provide indirect evidence against the hypothesis that the antiarrhythmic effects of amiodarone are mediated through a decrease in the serum T3 presented to the peripheral tissues.

胺碘酮与苯碘酮对甲状腺素代谢及体表心电图影响的比较。
本研究探讨了胺碘酮对心脏的电生理作用是否通过其对甲状腺素代谢的作用来介导。分别对15例胺碘酮(15例)和15例苯碘酮(15例)用药前后的血清甲状腺激素和心电图进行评估。胺碘酮和苯并碘酮均使外周甲状腺素的转化(胺碘酮P < 0.001,苯并碘酮P < 0.001)从三碘甲状腺原氨酸转向反三碘甲状腺原氨酸,同时两种药物均使TSH水平先降后升。胺碘酮治疗后心率降低(P < 0.025),校正心率的PR (P < 0.005)和QT间期(P < 0.005)升高。与苯碘酮相比,PR间期缩短(P < 0.05)。由于两种药物对甲状腺激素代谢的影响大致相似,但在心电图上的影响不同,因此我们的研究结果为胺碘酮抗心律失常作用是通过降低呈献给外周组织的血清T3来介导的这一假设提供了间接证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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