Reeves R A, From G L, Paul W, Leenen F H
Clin Pharmacol Ther. 1985 Feb;37(2):157-61. doi: 10.1038/clpt.1985.28.
Ten normal subjects participated in a placebo-controlled, randomized, parallel study to determine the effects on thyroid hormones of chronic (4 wk) propranolol or nadolol, including observation for 2 wk after their discontinuation. Subjects took placebo for 1 wk, then propranolol or nadolol doses increased weekly to 240 mg/day by 3 wk. After 1 wk of placebo, after 2 wk of the highest dose of propranolol or nadolol, and 2, 4, 6, 9, and 13 days after their discontinuation, thyroid hormone levels were measured by radioimmunoassay and heart rate responses to exercise were assessed. Both drugs induced equal and high degrees of exercise tachycardia inhibition. Propranolol decreased 3,3'5-triiodothyronine (T3) levels, increased 3-3'-5'-triiodothyronine (rT3) levels, tended to increase thyroxine levels, but did not increase thyroid-stimulating hormone levels. After discontinuation of propranolol, rT3 levels slowly (day 6) returned to values after placebo, suggesting delayed recovery of 5'-deiodination. There was no evidence of any rebound in T3 levels after withdrawal of propranolol. Nadolol induced no significant changes in the thyroid hormones measured. The data agree with the known effects of propranolol on thyroid hormones in normal man and show that nadolol does not have these effects when given chronically at an equivalent beta-blocking dose. The likely explanation is that the membrane-stabilizing activity of propranolol alters thyroid physiology by interfering with 5'-deiodinase.
10名正常受试者参与了一项安慰剂对照、随机、平行研究,以确定慢性(4周)普萘洛尔或纳多洛尔对甲状腺激素的影响,包括停药后2周的观察。受试者服用安慰剂1周,然后普萘洛尔或纳多洛尔剂量每周增加,至第3周时达到240毫克/天。在服用安慰剂1周后、服用普萘洛尔或纳多洛尔最高剂量2周后以及停药后2、4、6、9和13天,通过放射免疫分析法测量甲状腺激素水平,并评估运动时的心率反应。两种药物均引起同等程度且高度的运动性心动过速抑制。普萘洛尔降低了3,3',5-三碘甲状腺原氨酸(T3)水平,升高了3,3',5'-三碘甲状腺原氨酸(反T3,rT3)水平,甲状腺素水平有升高趋势,但未升高促甲状腺激素水平。停用普萘洛尔后,反T3水平缓慢(第6天)恢复至服用安慰剂后的水平,提示5'-脱碘作用恢复延迟。停用普萘洛尔后,没有证据表明T3水平有任何反跳。纳多洛尔对所测甲状腺激素未引起显著变化。这些数据与普萘洛尔对正常人体内甲状腺激素的已知作用相符,并表明纳多洛尔在等效β受体阻断剂量下长期给药时没有这些作用。可能的解释是,普萘洛尔的膜稳定活性通过干扰5'-脱碘酶改变了甲状腺生理功能。