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促甲状腺激素释放激素对大鼠垂体促甲状腺激素生物合成的翻译前和翻译后调节的不一致作用。

Discordant effects of thyrotropin (TSH)-releasing hormone on pre- and posttranslational regulation of TSH biosynthesis in rat pituitary.

作者信息

Lippman S S, Amr S, Weintraub B D

出版信息

Endocrinology. 1986 Jul;119(1):343-8. doi: 10.1210/endo-119-1-343.

Abstract

To investigate whether TRH regulates TSH production through a pre- or posttranslational mechanism, we determined the pituitary levels of mRNAs for alpha-subunit and TSH beta in male Sprague-Dawley rats given TRH in the presence or absence of thyroid hormones, with or without hypothalamic influence. In normal rats, serum TSH increased 6-fold after a single sc injection of TRH (7 micrograms/kg BW), but the levels of mRNA for both TSH subunits did not differ from the control values. Infusion of TRH, achieved by osmotic minipumps that were implanted sc, increased serum TSH for 3 days. Conversely, the pituitary content of TSH dropped to and remained 35% of that in the controls. In these normal rats, throughout the TRH infusion, the pituitary levels of mRNA for the TSH subunits did not differ from those in the controls. Thyroidectomy increased, by 27 and 75 times, the normal levels of mRNAs for alpha and TSH beta, respectively. TRH, given either as a single injection or a 3-day infusion, did not further elevate these levels. We then studied thyroidectomized animals whose pituitaries were transplanted under their renal capsules. These pituitaries responded to TRH infusion by releasing TSH. T4 injection inhibited this response significantly, but not completely. In spite of this evidence of normal responsiveness to TRH, infusion of TRH for a week did not increase the level of mRNAs for either TSH subunit in transplanted pituitaries. We conclude that in the presence or absence of thyroid hormones, with or without concurrent hypothalamic influence, TRH did not affect rat pituitary level of mRNA for either TSH subunit despite persistent high levels of serum TSH. Therefore, TRH does not regulate TSH production through a pretranslational mechanism. Although a translational regulation cannot be completely excluded, the present data, in conjunction with previous findings, support the hypothesis that TRH regulates TSH production primarily by stimulating both posttranslational carbohydrate processing and secretion of this hormone.

摘要

为研究促甲状腺激素释放激素(TRH)是通过翻译前还是翻译后机制调节促甲状腺激素(TSH)的产生,我们测定了在有或无甲状腺激素、有或无下丘脑影响的情况下,给予TRH的雄性Sprague-Dawley大鼠垂体中α亚基和TSHβ亚基的mRNA水平。在正常大鼠中,单次皮下注射TRH(7微克/千克体重)后,血清TSH增加了6倍,但两种TSH亚基的mRNA水平与对照值无差异。通过皮下植入的渗透微型泵输注TRH,可使血清TSH升高3天。相反,垂体中TSH的含量降至对照值的35%并维持在该水平。在这些正常大鼠中,在整个TRH输注过程中,TSH亚基的垂体mRNA水平与对照无差异。甲状腺切除分别使α亚基和TSHβ亚基的正常mRNA水平升高了27倍和75倍。单次注射或3天输注TRH均未进一步提高这些水平。然后我们研究了垂体移植到肾被膜下的甲状腺切除动物。这些垂体对TRH输注有反应,可释放TSH。注射T4可显著但未完全抑制这种反应。尽管有证据表明对TRH有正常反应,但输注TRH一周并未增加移植垂体中任一TSH亚基的mRNA水平。我们得出结论,无论有无甲状腺激素,有无同时存在的下丘脑影响,尽管血清TSH持续高水平,TRH均不影响大鼠垂体中任一TSH亚基的mRNA水平。因此,TRH不是通过翻译前机制调节TSH的产生。虽然不能完全排除翻译调节,但目前的数据与先前的研究结果一起支持了这样的假说,即TRH主要通过刺激该激素的翻译后糖基化加工和分泌来调节TSH的产生。

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