Glucocorticoids decrease the production of glucagon-like peptide-1 at the transcriptional level in intestinal L-cells

被引:7
|
作者
Sato, Taiki [1 ]
Hayashi, Hiroto [1 ]
Hiratsuka, Masahiro [1 ]
Hirasawa, Noriyasu [1 ]
机构
[1] Tohoku Univ, Grad Sch Pharmaceut Sci, Lab Pharmacotherapy Life Style Related Dis, Sendai, Miyagi 980, Japan
关键词
Glucocorticoids; Glucagon-like peptide-1; Intestinal L-cells; PROGLUCAGON GENE-EXPRESSION; INDUCED INSULIN-RESISTANCE; GASTRIN-RELEASING-PEPTIDE; MCA HYDROLYZING ENZYME; FREE FATTY-ACIDS; BETA-CATENIN; RECEPTOR; SECRETION; GLUCOSE; MECHANISMS;
D O I
10.1016/j.mce.2015.02.014
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glucocorticoids are widely used as anti-inflammatory or immunosuppressive drugs, but often induce hyperglycemia as a side effect. Glucagon-like peptide-1 (GLP-1) is secreted from intestinal L cells and plays crucial roles in maintaining glucose homeostasis. However, the direct effects of glucocorticoids on the GLP-1 production pathway in L cells remain unclear. We investigated the effects of glucocorticoids on GLP-1 production in vitro and in vivo. In L cell lines, glucocorticoids decreased GLP-1 release and expression of the precursor, proglucagon, at protein and mRNA levels, which were inhibited by mifepristone. The administration of dexamethasone or budesonide to mice significantly decreased the mRNA expression of proglucagon in the ileum and partially decreased glucose-stimulated GLP-1 secretion. Compound A, a dissociated glucocorticoid receptor modulator, did not affect the expression of proglucagon in vitro. These results suggested that glucocorticoids directly reduced GLP-1 production at the transcriptional level in L cells through a glucocorticoid receptor dimerization-dependent mechanism. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:60 / 67
页数:8
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