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氯贝丁酯及一种相关化合物可抑制原发性甲状腺功能减退症中的促甲状腺激素分泌。

Clofibrate and a related compound suppress TSH secretion in primary hypothyroidism.

作者信息

Kobayashi I, Shimomura Y, Maruta S, Ohshima K, Mori M, Kamio N, Fukuda H

出版信息

Acta Endocrinol (Copenh). 1980 May;94(1):53-7. doi: 10.1530/acta.0.0940053.

Abstract

A single oral dose of the hypolipidaemic agent ethyl-p-chlorophenoxyisobutyrate (clofibrate, 750 mg) produced a significant reduction on the high basal serum TSH level in patients with primary hypothyroidism. There was no consistent change in serum levels of thyroxine-iodine (T4-I), triiodothyronine (T3) and per cent free T4 (%FT4) during the study. On the other hand, clofibrate failed to produce discernible changes in the basal and TRH-induced TSH secretion in euthyroid subjects. Similar results were also obtained with the centrally active drug meclofenoxate hydrochloride (MH, 750 mg, drip infusion), similar in structure to clofibrate. These findings suggest that clofibrate and MH inhibit TSH secretion in patients with primary hypothyroidism, possibly by a direct action at the hypothalamic or pituitary level.

摘要

单次口服降血脂药物对氯苯氧异丁酸乙酯(安妥明,750毫克)可使原发性甲状腺功能减退患者较高的基础血清促甲状腺激素(TSH)水平显著降低。在研究期间,血清甲状腺素碘(T4-I)、三碘甲状腺原氨酸(T3)水平及游离T4百分比(%FT4)无一致变化。另一方面,安妥明未能使甲状腺功能正常的受试者基础及促甲状腺激素释放激素(TRH)诱导的TSH分泌产生明显变化。结构与安妥明相似的中枢活性药物盐酸甲氯芬酯(MH,750毫克,静脉滴注)也得到了类似结果。这些发现提示,安妥明和MH可能通过在下丘脑或垂体水平的直接作用来抑制原发性甲状腺功能减退患者的TSH分泌。

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