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石胆酸是维生素 D 受体配体,优先在回肠中起作用。

Lithocholic Acid Is a Vitamin D Receptor Ligand That Acts Preferentially in the Ileum.

机构信息

Division of Biochemistry, Department of Biomedical Sciences, Nihon University School of Medicine, 30-1 Oyaguchi-kamicho, Itabashi-ku, Tokyo 173-8610, Japan.

出版信息

Int J Mol Sci. 2018 Jul 6;19(7):1975. doi: 10.3390/ijms19071975.

Abstract

The vitamin D receptor (VDR) is a nuclear receptor that mediates the biological action of the active form of vitamin D, 1α,25-dihydroxyvitamin D₃ [1,25(OH)₂D₃], and regulates calcium and bone metabolism. Lithocholic acid (LCA), which is a secondary bile acid produced by intestinal bacteria, acts as an additional physiological VDR ligand. Despite recent progress, however, the physiological function of the LCA−VDR axis remains unclear. In this study, in order to elucidate the differences in VDR action induced by 1,25(OH)₂D₃ and LCA, we compared their effect on the VDR target gene induction in the intestine of mice. While the oral administration of 1,25(OH)₂D₃ induced the expression effectively in the duodenum and jejunum, the LCA increased target gene expression in the ileum as effectively as 1,25(OH)₂D₃. 1,25(OH)₂D₃, but not LCA, increased the expression of the calcium transporter gene in the upper intestine, and increased the plasma calcium levels. Although LCA could induce an ileal expression as well as 1,25(OH)₂D₃, the oral LCA administration was not effective in the VDR target gene induction in the kidney. No effect of LCA on the ileal expression was observed in the VDR-null mice. Thus, the results indicate that LCA is a selective VDR ligand acting in the lower intestine, particularly the ileum. LCA may be a signaling molecule, which links intestinal bacteria and host VDR function.

摘要

维生素 D 受体 (VDR) 是一种核受体,介导维生素 D 活性形式 1α,25-二羟维生素 D₃[1,25(OH)₂D₃]的生物学作用,并调节钙和骨骼代谢。胆酸(LCA)是肠道细菌产生的次级胆汁酸,作为额外的生理 VDR 配体起作用。然而,尽管最近取得了进展,LCA-VDR 轴的生理功能仍不清楚。在这项研究中,为了阐明 1,25(OH)₂D₃和 LCA 诱导的 VDR 作用的差异,我们比较了它们对小鼠肠道中 VDR 靶基因诱导的影响。虽然口服 1,25(OH)₂D₃能有效诱导十二指肠和空肠的表达,但 LCA 能像 1,25(OH)₂D₃一样有效诱导回肠靶基因的表达。1,25(OH)₂D₃,而不是 LCA,增加了上肠钙转运基因的表达,并增加了血浆钙水平。虽然 LCA 能像 1,25(OH)₂D₃一样诱导回肠表达,但口服 LCA 对肾脏中 VDR 靶基因的诱导没有效果。在 VDR 缺失小鼠中,LCA 对回肠表达没有影响。因此,结果表明 LCA 是一种选择性的 VDR 配体,在小肠,特别是回肠中起作用。LCA 可能是一种信号分子,它将肠道细菌和宿主 VDR 功能联系起来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c82d/6073204/dd630ae8613d/ijms-19-01975-g0A1.jpg

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