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普萘洛尔具有直接的抗甲状腺活性:抑制培养的甲状腺滤泡中的碘转运。

Propranolol has direct antithyroid activity: inhibition of iodide transport in cultured thyroid follicles.

作者信息

Murakami S, Nasu M, Fukayama H, Krishnan L, Sugawara M

机构信息

Division of Endocrinology and Metabolism, Research and Medical Services, Veterans Affair, West Los Angeles Medical Center, CA.

出版信息

Cell Biochem Funct. 1993 Sep;11(3):159-65. doi: 10.1002/cbf.290110303.

Abstract

The effect of propranolol on the process of thyroid hormone formation was studied in a physiological culture system. Porcine thyroid follicles were preincubated with propranolol for 24 h. Iodide transport, iodine organification, and de novo thyroid hormone formation were measured by incubating these follicles with the mixture of carrier-free 0.1 microCi Na125I and 50 nM NaI for 2 to 6 h at 37 degrees C. A concentration of propranolol greater than 100 microM inhibited iodide transport in a dose-dependent manner; this inhibition was non-competitive with iodide and independent of thyrotropin (TSH). Reduced iodine organification and thyroid hormone formation was seen with 150 microM propranolol or greater. The inhibitory action of propranolol was not caused by beta-blocking activity, since D-propranolol (devoid of beta-blocking activity) inhibited iodide transport, and other beta-blockers (metoprolol, atenolol, and labetalol) did not inhibit iodide transport. The inhibition of iodide transport was most likely caused by membrane stabilizing activity since quinidine, which possesses the same membrane stabilizing activity as propranolol, also inhibited iodide transport. TSH-mediated cAMP generation and Na+K+ ATPase activity, membrane functions for iodide transport, were unaffected by propranolol. Our study has shown, for the first time, that propranolol has a direct antithyroid action, namely inhibition of iodide transport in the intact thyroid follicle.

摘要

在生理培养系统中研究了普萘洛尔对甲状腺激素形成过程的影响。将猪甲状腺滤泡与普萘洛尔预孵育24小时。通过在37℃下将这些滤泡与无载体的0.1微居里Na125I和50纳摩尔NaI的混合物孵育2至6小时,来测量碘转运、碘有机化和甲状腺激素的从头合成。浓度大于100微摩尔的普萘洛尔以剂量依赖方式抑制碘转运;这种抑制作用与碘无竞争性,且不依赖于促甲状腺激素(TSH)。150微摩尔或更高浓度的普萘洛尔会导致碘有机化和甲状腺激素形成减少。普萘洛尔的抑制作用不是由β受体阻断活性引起的,因为D - 普萘洛尔(无β受体阻断活性)抑制碘转运,而其他β受体阻滞剂(美托洛尔、阿替洛尔和拉贝洛尔)不抑制碘转运。碘转运的抑制很可能是由膜稳定活性引起的,因为奎尼丁与普萘洛尔具有相同的膜稳定活性,也抑制碘转运。TSH介导的cAMP生成和Na + K + ATP酶活性(碘转运的膜功能)不受普萘洛尔影响。我们的研究首次表明,普萘洛尔具有直接的抗甲状腺作用,即在完整的甲状腺滤泡中抑制碘转运。

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