Anterior pituitary: triiodothyronine and/or dexamethasone induced changes in protein formation in thyroidectomized and/or adrenalectomized rats.

Endocrinologia experimentalis Pub Date : 1990-03-01
J Brtko, J Knopp, N H Scherberg
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Abstract

Protein formation in the anterior pituitary was investigated in vitro in thyroidectomized (TX) and/or adrenalectomited (AX) rats treated with a single dose of 100 micrograms/100 g of 3,5,3'-triiodothyronine (T3) and/or with a single dose of 10 micrograms/100 g of dexamethazone (DEX) 12 h before sacrifice. Male Wistar rats of a specific pathogen free colony 6 weeks after TX and/or AX receiving 1% calcium chloride and/or saline after surgery were used in the experiments. Non-pooled anterior pituitaries (in acellular condition) complemented with all essential amino acids, CPK, creatine phosphate in a HEPES buffer containing potassium acetate, magnesium acetate and dithiothreitol, were incubated with 35S-methionine at 28 degrees C for 10 or 40 min. The reaction was stopped by EDTA followed by RNAase plus DNAase treatment and the samples were analyzed for total 35S-methionine incorporation or by SDS 12.5% polyacrylamide gel slab electrophoresis (PAGE). As compared to intact rats (100%), TX and/or AX caused a significant diminution of the total 35S-methionine incorporation into protein ranging from 33% to 68% that may be easily restored to 107% by T3 plus DEX treatment. PAGE analysis reflects an appreciable relation between T3 administration and 21.5 kDa protein (growth hormone) formation in the anterior pituitary. In addition, the effect 5,5'-diphenylhydantoine (DPH) on 35S-methionine incorporation in relation to T3 nuclear specific binding was investigated. The data suggest that the decreased protein synthesis de novo is due to a significant diminution of T3 specific binding to nuclear receptors in the anterior pituitary.

垂体前叶:三碘甲状腺原氨酸和/或地塞米松诱导去甲状腺和/或去肾上腺大鼠蛋白形成的改变。
体外研究了去甲状腺(TX)和(或)去肾上腺(AX)大鼠在牺牲前12小时单剂量给药100微克/100克3,5,3′-三碘甲状腺原氨酸(T3)和/或单剂量10微克/100克地塞米松(DEX)后垂体前叶蛋白的形成。雄性Wistar大鼠在手术后接受1%氯化钙和/或生理盐水治疗,在TX和/或AX治疗6周后获得特定的无病原体菌落。在含有乙酸钾、乙酸镁和二硫苏糖醇的HEPES缓冲液中,与35s -蛋氨酸在28℃下孵育10或40分钟。用EDTA停止反应,然后用RNAase加DNAase处理,分析样品中35s -蛋氨酸的总含量或用SDS - 12.5%聚丙烯酰胺凝胶平板电泳(PAGE)分析。与完整大鼠(100%)相比,TX和/或AX使蛋白中35s -蛋氨酸的掺入量显著减少,减少幅度为33% - 68%,而T3加DEX处理后很容易恢复到107%。PAGE分析显示T3与垂体前叶21.5 kDa蛋白(生长激素)形成有明显关系。此外,还研究了5,5′-二苯基海因(DPH)对35s -蛋氨酸结合与T3核特异性结合的影响。这些数据表明,新生蛋白合成的减少是由于垂体前叶T3特异性结合核受体的显著减少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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