Department of Urology, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
Nucl Med Biol. 2013 Jul;40(5):643-50. doi: 10.1016/j.nucmedbio.2013.03.006. Epub 2013 Apr 22.
Renal uptake of Tc-99m-MG3 involves organic anion transporter (OAT). Treatment with drugs showing OAT affinity might interfere with renal uptake of Tc-99m-MAG3, leading to misinterpretation in Tc-99m-MAG3. This study was conducted to discuss a possible drug interference with Tc-99m-MAG3 diagnosis on OAT sites.
Renal uptake and plasma clearance of Tc-99m-MAG3 were analyzed in healthy volunteers under control and OAT1 and OAT3 related drug treatment conditions. An in vitro uptake study using OAT1 or OAT3 expressing cells was also conducted.
Both PAH and probenecid treatment induced delays in Tc-99m-MAG3 clearance from blood, and reductions in the renal uptake clearance. As a result, the normalized effective renal plasma flow estimated from Tc-99m-MAG3 clearance was significantly underestimated, whereas the glomerular filtration rate estimated from plasma creatinine levels was unchanged. The transport activity of Tc-99m-MAG3 was higher in OAT1-expressing cells than in OAT3-expressing cells.
Drugs with OAT1 affinity affect the renal uptake of Tc-99m-MAG3 and blood clearance. This might cause misinterpretation of functional diagnosis of the kidney using Tc-99m-MAG3.
Tc-99m-MG3 的肾脏摄取涉及有机阴离子转运体 (OAT)。具有 OAT 亲和力的药物治疗可能会干扰 Tc-99m-MAG3 的肾脏摄取,导致 Tc-99m-MAG3 的解读错误。本研究旨在探讨 OAT 部位的可能药物干扰 Tc-99m-MAG3 诊断。
在健康志愿者中,在对照和 OAT1 和 OAT3 相关药物治疗条件下分析 Tc-99m-MAG3 的肾脏摄取和血浆清除率。还进行了使用 OAT1 或 OAT3 表达细胞的体外摄取研究。
PAH 和丙磺舒治疗均导致 Tc-99m-MAG3 从血液中的清除延迟,并降低肾脏摄取清除率。结果,从 Tc-99m-MAG3 清除率估计的归一化有效肾血浆流量显着低估,而从血浆肌酐水平估计的肾小球滤过率不变。Tc-99m-MAG3 的转运活性在 OAT1 表达细胞中高于 OAT3 表达细胞。
具有 OAT1 亲和力的药物会影响 Tc-99m-MAG3 的肾脏摄取和血液清除。这可能导致使用 Tc-99m-MAG3 对肾脏功能诊断的错误解读。