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胃饥饿素介导的对体外分化人甲状腺细胞促甲状腺激素刺激功能的抑制作用。

Ghrelin-mediated inhibition of the TSH-stimulated function of differentiated human thyrocytes ex vivo.

作者信息

Barington Maria, Brorson Marianne Møller, Hofman-Bang Jacob, Rasmussen Åse Krogh, Holst Birgitte, Feldt-Rasmussen Ulla

机构信息

Department of Medical Endocrinology, Rigshospitalet, University Hospital Copenhagen, Copenhagen, Denmark.

Institute of Pharmacology, Department of Neuroscience and Pharmacology, University of Copenhagen, Copenhagen, Denmark.

出版信息

PLoS One. 2017 Sep 20;12(9):e0184992. doi: 10.1371/journal.pone.0184992. eCollection 2017.

Abstract

Ghrelin is a peptide hormone produced mainly in the gastrointestinal tract known to regulate several physiological functions including gut motility, adipose tissue accumulation and hunger sensation leading to increased bodyweight. Studies have found a correlation between the plasma levels of thyroid hormones and ghrelin, but an effect of ghrelin on the human thyroid has never been investigated even though ghrelin receptors are present in the thyroid. The present study shows a ghrelin-induced decrease in the thyroid-stimulating hormone (TSH)-induced production of thyroglobulin and mRNA expression of thyroperoxidase in a primary culture of human thyroid cells obtained from paranodular tissue. Accordingly, a trend was noted for an inhibition of TSH-stimulated expression of the sodium-iodine symporter and the TSH-receptor. Thus, this study suggests an effect of ghrelin on human thyrocytes and thereby emphasizes the relevance of examining whether ghrelin also influences the metabolic homeostasis through altered thyroid hormone production.

摘要

胃饥饿素是一种主要在胃肠道产生的肽类激素,已知它可调节多种生理功能,包括肠道蠕动、脂肪组织积累和饥饿感,从而导致体重增加。研究发现甲状腺激素的血浆水平与胃饥饿素之间存在相关性,但尽管甲状腺中存在胃饥饿素受体,胃饥饿素对人类甲状腺的影响从未被研究过。本研究表明,在从甲状腺旁组织获得的人甲状腺细胞原代培养物中,胃饥饿素可导致促甲状腺激素(TSH)诱导的甲状腺球蛋白产生减少以及甲状腺过氧化物酶的mRNA表达降低。因此,观察到胃饥饿素对TSH刺激的钠碘同向转运体和TSH受体表达有抑制趋势。因此,本研究提示胃饥饿素对人甲状腺细胞有作用,从而强调了研究胃饥饿素是否也通过改变甲状腺激素产生来影响代谢稳态的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b63c/5607171/28c7e28f0252/pone.0184992.g001.jpg

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