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首页> 外文期刊>American Journal of Physiology >The calcimimetic R-568 increases vitamin D receptor expression in rat parathyroid glands.
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The calcimimetic R-568 increases vitamin D receptor expression in rat parathyroid glands.

机译:拟钙剂R-568增加大鼠甲状旁腺中维生素D受体的表达。

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We previously demonstrated that extracellular calcium regulates vitamin D receptor (VDR) expression by parathyroid cells. Since the calcimimetic R-568 potentiates the effects of calcium on the calcium-sensing receptor, it was hypothesized that administration of R-568 may result in increased VDR expression in parathyroid tissue. In vitro studies of the effect of R-568 on VDR mRNA and protein were conducted in cultures of whole rat parathyroid glands and human hyperplastic parathyroid glands. In vivo studies in Wistar rats examined the effect of R-568 and calcitriol alone and in combination. Incubation of rat parathyroid glands in vitro with R-568 (0.001-1 microM) resulted in a dose-dependent decrease in parathyroid hormone (PTH) secretion and an increase in VDR expression (mean +/- SE). Incubation in 1 mM calcium + 0.001 microM R-568 elicited an increase in VDR mRNA (306 +/- 46%) similar to the maximum increase detected with 1.5 mM calcium (330 +/- 42%). In vivo, VDR mRNA was increased after administration of R-568 (168 +/- 9%, P < 0.001 vs. control) or calcitriol (198 +/- 16%, P < 0.001 vs. control). Treatment with R-568 also increased VDR protein in normal rat parathyroid glands and in human parathyroid glands with diffuse, but not nodular, hyperplasia. In conclusion, the present study shows that the calcimimetic R-568 exerts a stimulatory effect on VDR expression in the parathyroid glands of study models and provides additional evidence for the use of calcimimetics in the treatment of secondary hyperparathyroidism.
机译:我们先前证明细胞外钙调节甲状旁腺细胞的维生素D受体(VDR)表达。由于拟钙剂R-568增强了钙对钙敏感受体的作用,因此假设R-568的使用可能导致甲状旁腺组织中VDR表达增加。在整个大鼠甲状旁腺和人增生性甲状旁腺的培养物中进行了R-568对VDR mRNA和蛋白质影响的体外研究。 Wistar大鼠体内研究检查了R-568和骨化三醇单独使用或联合使用的效果。用R-568(0.001-1 microM)在体外对大鼠甲状旁腺进行孵育会导致甲状旁腺激素(PTH)分泌的剂量依赖性降低和VDR表达的增加(平均值+/- SE)。在1 mM钙+ 0.001 microM R-568中孵育会导致VDR mRNA增加(306 +/- 46%),与1.5 mM钙(330 +/- 42%)检测到的最大增加相似。在体内,施用R-568(168 +/- 9%,对对照,P <0.001)或骨化三醇(198 +/- 16%,对对照,P <0.001)后,VDR mRNA升高。在正常大鼠甲状旁腺和具有弥漫性但非结节性增生的人甲状旁腺中,用R-568进行治疗也会增加VDR蛋白。总之,本研究表明拟钙剂R-568对研究模型甲状旁腺中VDR表达具有刺激作用,并为拟钙剂在继发性甲状旁腺功能亢进中的应用提供了额外的证据。

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