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胺碘酮抑制大鼠肝脏中甲状腺素(T4)向三碘甲状腺原氨酸(T3)的转化以及α-磷酸甘油脱氢酶和苹果酸酶的水平。

Amiodarone inhibits T4 to T3 conversion and alpha-glycerophosphate dehydrogenase and malic enzyme levels in rat liver.

作者信息

Pekary A E, Hershman J M, Reed A W, Kannon R, Wang Y S

出版信息

Horm Metab Res. 1986 Feb;18(2):114-8. doi: 10.1055/s-2007-1012245.

Abstract

Amiodarone has been found to decrease serum T3 by blocking peripheral T4 5'-deiodinase. This reduction in T3 levels may contribute to the effectiveness of this drug in moderating cardiac arrhythmias. To further characterize the effect of amiodarone on thyroid hormone metabolism and biological action, male Sprague-Dawley rats were thyroidectomized and then fed 500 ug T4 or 50 ug T3 and 500 mg amiodarone/kg of powdered diet for 6 to 8 weeks. Hepatic and cardiac levels of T4, T3, alpha-glycerophosphate dehydrogenase (GPD) and malic enzyme (ME) were used as indicators of thyroid hormone availability and action at the cellular level. Conversion of T4 to T3 was measured in liver homogenates. Serum TSH, T4 and T3 were also measured. Amiodarone reduced hepatic GPD and ME in thyroidectomized rats receiving dietary T4. Liver T4 levels were significantly increased by amiodarone and the T3/T4 ratio was reduced (P less than .05). Amiodarone inhibited hepatic T4 to T3 conversion and decreased serum T3. The decreased T3 action at the cellular level, indicated by the reduction in hepatic GPD and ME, is not due to pharmacologic effects of amiodarone since these enzyme levels were not affected by amiodarone in thyroidectomized rats replaced with T3.

摘要

已发现胺碘酮可通过阻断外周T4 5'-脱碘酶来降低血清T3水平。T3水平的这种降低可能有助于该药物在缓解心律失常方面的有效性。为了进一步明确胺碘酮对甲状腺激素代谢和生物学作用的影响,对雄性Sprague-Dawley大鼠进行甲状腺切除,然后给予500μg T4或50μg T3以及500mg胺碘酮/千克粉状饲料,持续6至8周。肝脏和心脏中T4、T3、α-甘油磷酸脱氢酶(GPD)和苹果酸酶(ME)的水平被用作细胞水平上甲状腺激素可利用性和作用的指标。在肝脏匀浆中测定T4向T3的转化。还测定了血清促甲状腺激素(TSH)、T4和T3。胺碘酮降低了接受饮食T4的甲状腺切除大鼠肝脏中的GPD和ME。胺碘酮使肝脏T4水平显著升高,T3/T4比值降低(P小于0.05)。胺碘酮抑制肝脏T4向T3的转化并降低血清T3。肝脏GPD和ME降低所表明的细胞水平上T3作用的降低并非由于胺碘酮的药理作用,因为在用T3替代的甲状腺切除大鼠中,这些酶水平不受胺碘酮影响。

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