Suppr超能文献

1β,25-二羟维生素D3是1α,25-二羟维生素D3刺激的快速钙转运(肠道钙转运的快速激素刺激)的拮抗剂。

1 beta, 25 (OH)2-vitamin D3 is an antagonist of 1 alpha,25 (OH)2-vitamin D3 stimulated transcaltachia (the rapid hormonal stimulation of intestinal calcium transport).

作者信息

Norman A W, Nemere I, Muralidharan K R, Okamura W H

机构信息

Department of Biochemistry, University of California, Riverside 92521.

出版信息

Biochem Biophys Res Commun. 1992 Dec 30;189(3):1450-6. doi: 10.1016/0006-291x(92)90237-f.

Abstract

The steroid hormone 1 alpha,25-dihydroxyvitamin-D3 [1 alpha,25(OH)2D3] stimulates biological responses via both genomic mechanisms and nongenomic mechanisms (opening of voltage-gated Ca2+ channels). We report here that 1 beta, 25(OH)2-vitamin-D3 (a) is devoid of activity as an agonist for transcaltachia, (b) is a potent stereospecific antagonist of 1 alpha,25 (OH)2D3 stimulation of the nongenomic transcaltachia response and also (c) has less than 1% the ability of 1 alpha,25(OH)2D3 to bind to the chick intestinal nuclear 1 beta,25(OH)2D3 receptor. We conclude that the membrane response element(s) which generates the nongenomic response of transcaltachia has a different ligand specificity than the classic nuclear 1 alpha, 25(OH)2D3 receptor.

摘要

类固醇激素1α,25 - 二羟基维生素D3 [1α,25(OH)2D3] 通过基因组机制和非基因组机制(电压门控Ca2+通道开放)刺激生物学反应。我们在此报告,1β,25(OH)2 - 维生素D3:(a) 作为转钙素激动剂无活性;(b) 是1α,25(OH)2D3刺激非基因组转钙素反应的强效立体特异性拮抗剂;并且(c) 与1α,25(OH)2D3相比,其与鸡肠细胞核1β,25(OH)2D3受体结合的能力不到1%。我们得出结论,产生转钙素非基因组反应的膜反应元件具有与经典核1α,25(OH)2D3受体不同的配体特异性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验