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关于L-甲状腺素在垂体水平起主要作用的证据不足:对用碘番酸(telepaque)治疗的大鼠的研究。

Evidence against a major role of L-thyroxine at the pituitary level: studies in rats treated with iopanoic acid (telepaque).

作者信息

Obregon M J, Pascual A, Mallol J, Morreale de Escobar G, Escobar del Rey F

出版信息

Endocrinology. 1980 Jun;106(6):1827-36. doi: 10.1210/endo-106-6-1827.

Abstract

To determine whether T4 has an intrinsic effect at the pituitary level, it would be important to block conversion of T4 to T3 completely. We have attempted to achieve this with iopanoic acid (IOP), a radiographic contrast agent. We have then measured in the same animals the effects of such treatment on the conversion of T4 to T3 or on the deiodination of T3 and on the pituitary response to a dose of T4 or T3. Plasma TSH levels and pituitary GH content were measured as biological end points. Thyroidectomized rats were injected with a single dose of T4 (1.7 micrograms/100 g BW) labeled with [125I]T4 (Exp A) or with a single dose of T3 (0.33 microgram/100 g BW) labeled with [125I]T3 (Exp B) and treated with IOP or solvent. Animals of Exp A were killed 24 h after iodothyronine injection and those of Exp B were killed 4, 12, and 24 h after injection of the iodothyronine. The concentrations of [125I]T4 and [125I]T3 were measured in several tissues, including the anterior pituitary, after extraction and paper chromatography and quantified with the aid of 131I-labeled markers added in vitro. Plasma and pituitary T3 and T4 plasma TSH, and pituitary GH were measured by specific RIAs. Results show that treatment with IOP markedly inhibits the conversion of T4 to T3 and the deiodination of T3. In IOP-treated thyroidectomized rats, the injection of T4 results in little, if any, effect at the pituitary level, despite an almost 3-fold increase in the percentage of injected T4 found in the gland. Treatment with IOP does not inhibit the effects of a T3 dose; if anything, they appear to be enhanced. It is concluded that, as assessed from biological responses involving the anterior pituitary, a dose of T4 has little if any effect other than that which can be attributed to the T3 generated from it.

摘要

为了确定T4在垂体水平是否具有内在作用,完全阻断T4向T3的转化至关重要。我们尝试使用造影剂碘番酸(IOP)来实现这一点。然后我们在相同的动物中测量了这种处理对T4向T3转化、T3脱碘以及垂体对一定剂量T4或T3反应的影响。测量血浆促甲状腺激素(TSH)水平和垂体生长激素(GH)含量作为生物学终点。给甲状腺切除的大鼠注射单剂量用[125I]T4标记的T4(1.7微克/100克体重)(实验A)或单剂量用[125I]T3标记的T3(0.33微克/100克体重)(实验B),并用IOP或溶剂处理。实验A的动物在注射碘甲状腺原氨酸后24小时处死,实验B的动物在注射碘甲状腺原氨酸后4、12和24小时处死。在包括垂体前叶在内的多个组织中,经过提取和纸层析后测量[125I]T4和[125I]T3的浓度,并借助体外添加的131I标记物进行定量。通过特异性放射免疫分析(RIA)测量血浆和垂体中的T3、T4、血浆TSH以及垂体GH。结果表明,用IOP处理可显著抑制T4向T3的转化以及T3的脱碘。在经IOP处理的甲状腺切除大鼠中,注射T4在垂体水平几乎没有影响,尽管腺体中注射的T4百分比几乎增加了3倍。用IOP处理并不抑制T3剂量的作用;如果有什么不同的话,它们似乎增强了。结论是,从前叶垂体的生物学反应评估,一定剂量的T4除了可归因于由其生成的T3的作用外,几乎没有其他作用。

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