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培养的人垂体细胞中促甲状腺激素释放的神经内分泌调节

Neuroendocrine regulation of thyrotropin release in cultured human pituitary cells.

作者信息

Abrahamson M J, Wormald P J, Millar R P

机构信息

Department of Medicine, University of Cape Town, South Africa.

出版信息

J Clin Endocrinol Metab. 1987 Dec;65(6):1159-63. doi: 10.1210/jcem-65-6-1159.

Abstract

The regulation of TSH release in man was investigated using cell cultures derived from human pituitaries obtained within 24 h of accidental death. TRH stimulated TSH release in a dose-dependent manner. The ED50 was 2.9 +/- 0.6 (+/- SEM) nmol/L, similar to that reported for rat pituitary cell cultures. The release of TSH was calcium dependent, since the calcium channel antagonist verapamil inhibited TRH-stimulated TSH release, and the calcium ionophore A23187 stimulated TSH release. 12-O-Tetradecanoyl-phorbol-13-acetate stimulated TSH secretion, while dibuytryl cAMP had no effect. Epinephrine and serotonin stimulated TSH release, and dopamine and somatostatin inhibited TRH-stimulated TSH release. These findings have directly demonstrated that the regulation of TSH secretion by hypothalamic neuropeptides and biogenic amines in the human pituitary is similar to that in the rat. The development of a tissue culture system to study thyrotrophs from postmortem human pituitaries provides the means for detailed studies of the regulation of TSH secretion in man.

摘要

利用意外死亡后24小时内获取的人垂体来源的细胞培养物,对人类促甲状腺激素(TSH)释放的调节进行了研究。促甲状腺激素释放激素(TRH)以剂量依赖的方式刺激TSH释放。半数有效剂量(ED50)为2.9±0.6(±标准误)nmol/L,与报道的大鼠垂体细胞培养物的数值相似。TSH的释放依赖于钙,因为钙通道拮抗剂维拉帕米抑制TRH刺激的TSH释放,而钙离子载体A23187刺激TSH释放。12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯刺激TSH分泌,而二丁酰环磷腺苷(dibuytryl cAMP)则无作用。肾上腺素和血清素刺激TSH释放,多巴胺和生长抑素抑制TRH刺激的TSH释放。这些发现直接表明,人垂体中下丘脑神经肽和生物胺对TSH分泌的调节与大鼠相似。开发一种用于研究死后人类垂体促甲状腺细胞的组织培养系统,为详细研究人类TSH分泌的调节提供了手段。

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