Patel S, Hsu C H
Department of Internal Medicine, University of Michigan Medical School, Ann Arbor.
J Lab Clin Med. 1990 Jan;115(1):69-73.
Previous study from our laboratory has demonstrated that infusion of uremic plasma ultrafiltrate to normal rats suppressed their calcitriol synthesis. In order identify the uremic toxins responsible for the suppression of the calcitriol synthesis, we studied the effects of known uremic toxins: spermidine, spermine, methylguanidine (MG), and guanidinosuccinic acid (GSA) on calcitriol metabolism in the rats. Metabolic clearance rate (MCR) and production rate (PR) of calcitriol were measured in normal rats after they were infused for 24 hours with approximately 10 ml of normal saline containing one of the following substances: 0.8 mumoles spermidine, 0.3 mumoles spermine, 150 micrograms MG and 180 micrograms GSA. Control groups of rats were infused with 10 ml of normal saline for 24 hours. MCR of calcitriol was not altered by the infusion of each toxin; however, plasma concentration of calcitriol (controls, 105.3 +/- 6.7 pg/ml; versus GSA, 58.9 +/- 2.5 pg/ml, p less than 0.001) and PR of calcitriol (controls, 39.0 +/- 2.9 ng/kg/day, versus GSA, 22.5 +/- 1.62 ng/kg/day, p less than 0.001) were significantly suppressed by the infusion of GSA. The concentration (1.8 mg/dl) of GSA in the infusate was similar to that in the uremic plasma ultrafiltrate (2.32 +/- 1.41 mg/dl) used in the previous study, though the total amount of GSA infused to the rats was lower in the present study. GSA is, therefore, considered a uremic toxin that suppresses calcitriol synthesis.
我们实验室之前的研究表明,向正常大鼠输注尿毒症血浆超滤液会抑制其骨化三醇的合成。为了确定导致骨化三醇合成受抑制的尿毒症毒素,我们研究了已知尿毒症毒素:亚精胺、精胺、甲基胍(MG)和胍基琥珀酸(GSA)对大鼠骨化三醇代谢的影响。在正常大鼠被输注约10毫升含有以下物质之一的生理盐水24小时后,测量其骨化三醇的代谢清除率(MCR)和生成率(PR):0.8微摩尔亚精胺、0.3微摩尔精胺、150微克MG和180微克GSA。对照组大鼠输注10毫升生理盐水24小时。每种毒素的输注均未改变骨化三醇的MCR;然而,骨化三醇的血浆浓度(对照组,105.3±6.7皮克/毫升;与GSA组相比,58.9±2.5皮克/毫升,p<0.001)和骨化三醇的PR(对照组,39.0±2.9纳克/千克/天,与GSA组相比,22.5±1.62纳克/千克/天,p<0.001)在输注GSA后均被显著抑制。输注液中GSA的浓度(1.8毫克/分升)与之前研究中使用的尿毒症血浆超滤液中的浓度(2.32±1.41毫克/分升)相似,尽管本研究中输注给大鼠的GSA总量较低。因此,GSA被认为是一种抑制骨化三醇合成的尿毒症毒素。