Breidbach Andreas, Catlin Don H, Green Gary A, Tregub Inna, Truong Henry, Gorzek Jeffrey
UCLA Olympic Analytical Laboratory, University of California at Los Angeles, Los Angeles, CA 90025, USA.
Clin Chem. 2003 Jun;49(6 Pt 1):901-7. doi: 10.1373/49.6.901.
Doping with erythropoietic proteins such as recombinant human erythropoietin (rHuEPO) and darbepoetin alfa is a serious issue in sport. There is little information on the time course of detection of rHuEPO in urine and on methods to evaluate electrophoresis-based data.
We used a recently described isoelectric focusing method for detecting rHuEPO and endogenous EPO in urine obtained from individuals treated with placebo or epoetin alfa. The latter was administered subcutaneously at 50 IU/kg on days 0, 2, 4, 7, 9, 11, 14, 16, and 18. Blood and urine samples were collected during the morning of study days -3, 0, 2, 4, 7, 9, 11, 14, 16, and 18 and on days 2, 3, 4, and 7 postadministration. We developed visual and numerical (two-band ratio) techniques to evaluate the electropherograms for the presence of rHuEPO.
Compared with the placebo group, the epoetin alfa-treated group responded with increases in hematocrit, reticulocytes, macrocytes, serum EPO, and serum soluble transferrin receptor. The electropherograms showed that the pattern of bands arising from urinary rHuEPO is different from that of endogenous urinary EPO. Both the two-band ratio and the visual technique detected rHuEPO in all 14 epoetin alfa-treated individuals 3 days after the last dose. On the 7th day after the last dose, both techniques detected rHuEPO in approximately one-half of the participants. rHuEPO was not detected in the placebo-treated individuals.
The isoelectric focusing method detects rHuEPO in most urine samples collected 3 days after nine doses of epoetin alfa. The numerical two-band ratio was equivalent to a visual method for detecting rHuEPO in urine.
使用促红细胞生成蛋白,如重组人促红细胞生成素(rHuEPO)和阿法达贝泊汀,在体育界是一个严重问题。关于尿液中rHuEPO的检测时间进程以及评估基于电泳数据的方法的信息很少。
我们使用最近描述的等电聚焦方法,检测从接受安慰剂或阿法依泊汀治疗的个体获得的尿液中的rHuEPO和内源性EPO。后者在第0、2、4、7、9、11、14、16和18天以50 IU/kg的剂量皮下给药。在研究第-3、0、2、4、7、9、11、14、16和18天的早晨以及给药后第2、3、4和7天采集血液和尿液样本。我们开发了视觉和数值(双带比)技术,以评估电泳图谱中是否存在rHuEPO。
与安慰剂组相比,阿法依泊汀治疗组的血细胞比容、网织红细胞、大红细胞、血清EPO和血清可溶性转铁蛋白受体增加。电泳图谱显示,尿液中rHuEPO产生的条带模式与内源性尿液EPO不同。双带比和视觉技术在最后一剂后3天在所有14名接受阿法依泊汀治疗的个体中均检测到rHuEPO。在最后一剂后的第7天,两种技术在大约一半的参与者中检测到rHuEPO。在接受安慰剂治疗的个体中未检测到rHuEPO。
等电聚焦方法在九剂阿法依泊汀后3天采集的大多数尿液样本中检测到rHuEPO。数值双带比与检测尿液中rHuEPO的视觉方法等效。