Wells P G, Feely J, Wilkinson G R, Wood A J
Clin Pharmacol Ther. 1983 May;33(5):603-8. doi: 10.1038/clpt.1983.81.
The effects of thyrotoxicosis on Liver blood flow and propranolol disposition were followed in five patients while thyrotoxic and when euthyroid. Propranolol was taken orally to achieve steady state and then radiolabeled drug was given simultaneously by intravenous injection. Thyrotoxicosis was associated with doubling of both oral and systemic clearances of unbound propranolol, which resulted in an approximately 50% reduction in blood concentrations after oral doses. These changes were attributable to increases in hepatic blood flow and drug-metabolizing activity of the liver. The propranolol elimination t 1/2 was not affected by thyrotoxicosis since the enhanced clearance was offset by a change in volume of distribution. These findings may explain the reduction of plasma propranolol concentration and many of the therapeutic failures reported in the treatment of thyrotoxicosis. The dose required to achieve therapeutic blood concentrations of propranolol in thyrotoxic patients is variable and will usually be substantially larger than that required for euthyroid patients.
对五名甲状腺毒症患者在甲状腺毒症期和甲状腺功能正常期进行了甲状腺毒症对肝血流量和普萘洛尔处置的影响研究。口服普萘洛尔以达到稳态,然后通过静脉注射同时给予放射性标记药物。甲状腺毒症与未结合普萘洛尔的口服清除率和全身清除率加倍相关,这导致口服给药后血药浓度降低约50%。这些变化归因于肝血流量增加和肝脏药物代谢活性增强。普萘洛尔消除半衰期不受甲状腺毒症影响,因为清除率的提高被分布容积的变化所抵消。这些发现可能解释了甲状腺毒症治疗中血浆普萘洛尔浓度降低以及许多治疗失败的原因。在甲状腺毒症患者中达到普萘洛尔治疗血药浓度所需的剂量是可变的,通常会比甲状腺功能正常患者所需的剂量大得多。