Patel S R, Ke H Q, Vanholder R, Hsu C H
Department of Internal Medicine, University of Michigan Medical School, Ann Arbor.
Kidney Int. 1994 Jul;46(1):129-33. doi: 10.1038/ki.1994.252.
The biological action of calcitriol is mediated through a hormone-receptor complex interacting with nuclear chromatin. Interaction of the calcitriol receptor (VDR) with VDR response elements produces bioactive proteins which carry out the physiological actions of calcitriol. Since biological response to calcitriol appears to be diminished in renal failure, we studied the effect of uremic toxins on the interaction of VDR with nuclear chromatin using in vitro nuclear uptake of the 3H-calcitriol labeled VDR by intestinal nuclei. We found that nuclear uptake of the labeled intestinal VDR from renal failure rats was significantly lower than that from the control animals. HPLC fractionated uremic ultrafiltrate directly inhibited nuclear uptake of the labeled VDR when the labeled VDR was incubated with 50% of the ultrafiltrate for various time intervals ranging from 15 minutes to 6 hours. Infusion of uremic ultrafiltrate to normal rats for 20 hours also produced intestinal VDR with a lower binding affinity for intestinal nuclei when compared to the controls infused with normal ultrafiltrate. The latter study suggests that uremic toxins are responsible for the decreased nuclear uptake of VDR of rats with renal failure. Although it is difficult to extrapolate these results directly to the intact cells, our findings suggest that part of the calcitriol resistance in renal failure could be explained by decreased entry of receptor into the nucleus.
骨化三醇的生物学作用是通过与核染色质相互作用的激素 - 受体复合物介导的。骨化三醇受体(VDR)与VDR反应元件的相互作用产生生物活性蛋白,这些蛋白执行骨化三醇的生理作用。由于肾衰竭时对骨化三醇的生物学反应似乎减弱,我们使用肠细胞核对3H - 骨化三醇标记的VDR的体外核摄取来研究尿毒症毒素对VDR与核染色质相互作用的影响。我们发现,肾衰竭大鼠标记的肠VDR的核摄取明显低于对照动物。当标记的VDR与50%的超滤物在15分钟至6小时的不同时间间隔孵育时,HPLC分级分离的尿毒症超滤物直接抑制标记的VDR的核摄取。与输注正常超滤物的对照组相比,向正常大鼠输注尿毒症超滤物20小时也产生了对肠细胞核结合亲和力较低的肠VDR。后一项研究表明,尿毒症毒素是肾衰竭大鼠VDR核摄取减少的原因。尽管很难将这些结果直接外推到完整细胞,但我们的研究结果表明,肾衰竭中部分骨化三醇抵抗可以通过受体进入细胞核减少来解释。