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Effects of vitamin D, dietary calcium and vitamin D restriction, pregnancy and lactation on gene expression of calcium transporting factors

机译:维生素D,饮食中钙和维生素D的限制,妊娠和哺乳期对钙转运因子基因表达的影响

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摘要

The purpose of the first study was to determine the changes in intestinal vitamin D-dependent plasma membrane calcium ATPase (PMCA1) and calcium binding protein-9K (CaBP-9K) mRNA induced by a single injection of 1,25-D3 or 1,25,28-trihydroxyvitamin D2 (1,25,28-D2) in vitamin D-deficient rats. The results indicated that a single injection of 20 ng of 1,25-D3 per rat double intestinal PMCA1 mRNA at 4, 8, 12, hours and CaBP-9K mRNA at 8, 12, and 24 hours after injection. The mRNA of PMCA1 and CaBP-9K could be increased by a larger dose of 1,25,28-D2 (20 ng). These data suggest that the up-regulation of PMCA1 and CaBP-9K mRNA may be critical to active calcium transport;In the second study, the effect of dietary calcium and/or vitamin D-deficiency on intestinal PMCA1 and CaBP-9K mRNA expression in rats was examined. The results indicate both intestinal CaATPase and CaBP-9K mRNA are down-regulated in rats fed diets containing no vitamin D. However, our data suggest that dietary calcium restriction alone did not have any effect on CaATPase and CaBP mRNA. This study demonstrates that dietary calcium itself is probably not a regulator of mRNA gene expression of PMCA1 and CaBP-9K;In the third study, intestinal PMCA1, CaBP-9K and vitamin D receptor (VDR) mRNA were determined at different stages of pregnancy and early lactation in rats. At 21 days gestation and 7 days of lactation, both PMCA1 and CaBP-9K mRNA levels increased 2-3 fold. PMCA1 and CaBP-9K mRNA remained elevated at 7 days of lactation. Interestingly, VDR mRNA levels did not change during the entire experiment. However, VDR content increased 2-fold in late pregnancy and lactation. These data suggest that the effects of gestation and lactation on PMCA1 and CaBP-9K are probably transcriptional and on VDR are post transcriptional.
机译:第一项研究的目的是确定通过单次注射1,25-D3或1诱导的肠道维生素D依赖性质膜钙ATPase(PMCA1)和钙结合蛋白9K(CaBP-9K)mRNA的变化。缺乏维生素D的大鼠中的25,28-三羟基维生素D2(1,25,28-D2)。结果表明,在注射后第4、8、12、24小时每只大鼠单次注射20 ng 1,25-D3双肠PMCA1 mRNA,并在注射后8、12和24小时单次注射CaBP-9K mRNA。较大剂量的1,25,28-D2(20 ng)可以增加PMCA1和CaBP-9K的mRNA。这些数据表明PMCA1和CaBP-9K mRNA的上调可能对钙的主动转运至关重要;在第二项研究中,饮食中钙和/或维生素D缺乏对肠道PMCA1和CaBP-9K mRNA表达的影响。检查大鼠。结果表明,饲喂不含维生素D的大鼠肠道中CaATPase和CaBP-9K mRNA均下调。但是,我们的数据表明,仅饮食中限钙对CaATPase和CaBP mRNA没有任何影响。这项研究表明,饮食中的钙本身可能不是PMCA1和CaBP-9K mRNA基因表达的调节剂;在第三项研究中,在怀孕的不同阶段测定了肠道PMCA1,CaBP-9K和维生素D受体(VDR)mRNA。大鼠早期哺乳。在妊娠21天和哺乳7天时,PMCA1和CaBP-9K mRNA水平均增加2-3倍。哺乳期7天,PMCA1和CaBP-9K mRNA仍然升高。有趣的是,在整个实验过程中,VDR mRNA水平没有变化。但是,妊娠晚期和哺乳期的VDR含量增加了2倍。这些数据表明,妊娠和哺乳期对PMCA1和CaBP-9K的影响可能是转录的,而对VDR的影响是转录后的。

著录项

  • 作者

    Zhu, Yingting;

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  • 年度 1995
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  • 原文格式 PDF
  • 正文语种 en
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