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短链脂肪酸可增加大鼠垂体细胞GH3株中催乳素和生长激素的分泌,并改变细胞形态。

Short chain fatty acids increase prolactin and growth hormone production and alter cell morphology in the GH3 strain of rat pituitary cells.

作者信息

Yen P M, Tashjian A H

出版信息

Endocrinology. 1981 Jul;109(1):17-22. doi: 10.1210/endo-109-1-17.

DOI:10.1210/endo-109-1-17
PMID:7238401
Abstract

Treatment of GH3 cells for 24-72 h with sodium valerate (1 mM) increased 2- to 4-fold the production of both PRL and GH. There was a concomitant change in the morphology of the cells that resembled that produced by TRH and epidermal growth factor. The increases in hormone production and changes in morphology were reversible. The sodium salts of butyric, hexanoic, caprylic, nonanoic, and dodecanoic acids also increased hormone production and altered cell morphology, whereas the salts of formic, acetic, and isobutyric acids did not. Acute (1-h) treatment with the fatty acids, unlike the effects of TRH and epidermal growth factor, did not increase the release of PRL from the cells.

摘要

用戊酸钠(1 mM)处理GH3细胞24至72小时,可使催乳素(PRL)和生长激素(GH)的分泌增加2至4倍。细胞形态同时发生变化,类似于促甲状腺激素释放激素(TRH)和表皮生长因子所产生的变化。激素分泌的增加和形态变化是可逆的。丁酸、己酸、辛酸、壬酸和十二烷酸的钠盐也增加了激素分泌并改变了细胞形态,而甲酸、乙酸和异丁酸的盐则没有此作用。与TRH和表皮生长因子的作用不同,脂肪酸急性(1小时)处理并未增加细胞中PRL的释放。

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1
Short chain fatty acids increase prolactin and growth hormone production and alter cell morphology in the GH3 strain of rat pituitary cells.短链脂肪酸可增加大鼠垂体细胞GH3株中催乳素和生长激素的分泌,并改变细胞形态。
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Butyrate increases intracellular calcium levels and enhances growth hormone release from rat anterior pituitary cells via the G-protein-coupled receptors GPR41 and 43.丁酸盐可提高细胞内钙水平,并通过G蛋白偶联受体GPR41和43增强大鼠垂体前叶细胞释放生长激素。
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Short-chain fatty acids inhibit growth hormone and prolactin gene transcription via cAMP/PKA/CREB signaling pathway in dairy cow anterior pituitary cells.
短链脂肪酸通过奶牛腺垂体细胞中的 cAMP/PKA/CREB 信号通路抑制生长激素和催乳素基因转录。
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Adenosine 3',5'-cyclic monophosphate-dependent release of prolactin from GH3 pituitary tumour cells. A quantitative analysis.3',5'-环磷酸腺苷依赖的生长激素3型垂体瘤细胞催乳素释放。定量分析。
Biochem J. 1983 Dec 15;216(3):551-7. doi: 10.1042/bj2160551.
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