Aanderud S, Sundsfjord J, Aarbakke J
Endocrinology. 1984 Oct;115(4):1605-8. doi: 10.1210/endo-115-4-1605.
Previous studies have shown decreased T3 and increased T4 and rT3 serum levels in subjects treated with amiodarone. We studied the acute effect of amiodarone on the in vitro conversion of T4 to T3 in suspensions of isolated rat hepatocytes. Iodine and melperone, another class III antiarrhythmic drug, were included in the study as controls. Amiodarone (60 microM) totally blocked the formation of T3 from T4, whereas concentrations of 6 and 0.6 microM reduced T3 formation to 13.7 +/- 10.6% and 63.9 +/- 15.9% (+/- SD), respectively, compared with untreated controls. The drug solvent did not affect the conversion rate. Iodide (120 microM) had an inhibitory effect of approximately 10% compared with the controls, whereas melperone did not affect this in vitro conversion. Amiodarone (60 microM) caused a slight but significant reduction of the cellular uptake of [125I]T4 after 10 min of incubation, whereas the 60 min values were unaltered. Our study indicates that amiodarone inhibits the 5'-monodeiodination of T4 to T3 in a dose-related manner. It is suggested that the antiarrhythmic activity of the drug is related to its inhibitory effect on the conversion of T4 to T3.
以往的研究表明,接受胺碘酮治疗的患者血清中T3水平降低,T4和反T3水平升高。我们研究了胺碘酮对离体大鼠肝细胞悬液中T4向T3体外转化的急性影响。本研究将碘和另一类III类抗心律失常药物美哌隆作为对照。胺碘酮(60微摩尔)完全阻断了T4向T3的转化,而6微摩尔和0.6微摩尔的浓度分别使T3的生成量降至未处理对照组的13.7±10.6%和63.9±15.9%(±标准差)。药物溶剂不影响转化率。与对照组相比,碘化物(120微摩尔)具有约10%的抑制作用,而美哌隆不影响这种体外转化。孵育10分钟后,胺碘酮(60微摩尔)使[125I]T4的细胞摄取略有但显著减少,而60分钟时的值未改变。我们的研究表明,胺碘酮以剂量相关的方式抑制T4向T3的5'-单脱碘作用。提示该药物的抗心律失常活性与其对T4向T3转化的抑制作用有关。