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Effect of amiodarone on serum triiodothyronine, reverse triiodothyronine, thyroxin, and thyrotropin. A drug influencing peripheral metabolism of thyroid hormones.

机译:胺碘酮对血清三碘甲状腺素,反向三碘甲状腺素,甲状腺素和促甲状腺激素的影响。影响甲状腺激素外周代谢的药物。

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摘要

2-n-Butyl-3-(4'-diethylaminoethoxy-3',5'-diiodobenzoyl)-benzofurane (amiodarone), a drug used in arrythmias and angina pectoris, contains 75 mg of organic iodine/200 mg active substance. Four studies were performed to test its effect on thyroid hormone metabolism: (a) nine male subjects were treated with 400 mg of amiodarone for 28 days; (b) five male subjects received, for the same period of time, 150 mg of iodine in the form of Lugol's solution; (c) five subjects received 300 mug L-thyroxine (T4) for 16 days; from the 10th to the 16th day, 400 mg of amiodarone was added; and (d) five euthyroid subjects received 300 mug L-T4 for 16 days. The changes in serum thyroid-stimulating hormone (TSH), serum total T4, 3,5,3'-triiodothyronine (T3), free T3, and 3,5',3'-triiodothyronine (reverse T3, rT3) were measured, and the pituitary reserve in TSH was evaluated by a thyrotropin-releasing hormone (TRH) test. The results show that amiodarone induced a decrease in serum T3 (28+/-5.1 ng/100 ml, mean+/-SEM, P less than 0.0S and 82.7+/-9.3 ng rT3/100 ml, P less than 0.01). The control study with an equal amount of inorganic iodine did not induce these opposite changes but slightly lowered serum rT3, T3, and T4. In the third study, serum rT3 increased as under amiodarone treatment, thereby proving that these changes were peripheral. It is suggested that amiodarone changes thyroid hormone metabolism, possibly by reducing deiodination of T4 to T3 and inducing a preferential production of rT3. Amiodarone also increased the response of TSH to TRH. The maximal increment of serum TSH above base line was 32+/-4.5 muU/ml under treatment and 20+/-3 muU/ml before treatment (P less than 0.01). During this test, the serum T3 increase was more pronounced than during the control period (83+/-13 and 47+/-7.4 ng/100 ml, P less than 0.05).
机译:2-n-丁基-3-(4'-二乙基氨基乙氧基-3',5'-二碘苯甲酰基)-苯并呋喃(胺碘酮)是用于前卫性心律失常和心绞痛的药物,其中含有75 mg有机碘/ 200 mg活性物质。进行了四项研究以测试其对甲状腺激素代谢的影响:(a)9名男性受试者接受400 mg胺碘酮治疗28天; (b)五名男性受试者在同一时期接受卢戈尔溶液形式的150毫克碘; (c)五名受试者接受了300杯左旋甲状腺素(T4)治疗16天;从第10天到第16天,加入400mg胺碘酮; (d)五名甲状腺功能正常的受试者接受了300杯L-T4治疗,持续16天。测量了血清促甲状腺激素(TSH),血清总T4、3,5,3'-三碘甲腺氨酸(T3),游离T3和3,5',3'-三碘甲丙氨酸(反向T3,rT3)的变化,通过促甲状腺激素释放激素(TRH)试验评估TSH中的垂体储备。结果表明,胺碘酮可引起血清T3降低(28 +/- 5.1 ng / 100 ml,平均值+/- SEM,P小于0.0S和82.7 +/- 9.3 ng rT3 / 100 ml,P小于0.01)。用相同量的无机碘进行的对照研究未引起这些相反的变化,但使血清rT3,T3和T4略有降低。在第三项研究中,血清rT3随胺碘酮治疗而增加,从而证明这些变化是外周性的。提示胺碘酮可能通过减少T4的去碘化作用并诱导rT3的优先产生来改变甲状腺激素的代谢。胺碘酮还增加了TSH对TRH的反应。治疗后血清TSH的最大增量为32 +/- 4.5μU/ ml,治疗前为20 +/- 3μU/ ml(P小于0.01)。在此测试期间,血清T3的增加比对照期间更为明显(83 +/- 13和47 +/- 7.4 ng / 100 ml,P小于0.05)。

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