Weller S, Thürmann P, Rietbrock N, Gossmann J, Scheuermann E H
Department of Clinical Pharmacology, University Clinic Frankfurt/M, Germany.
Int J Clin Pharmacol Ther. 1995 Dec;33(12):639-45.
Anemia has been frequently reported in renal transplant recipients receiving azathioprine for immunosuppression and enalapril for treatment of hypertension. During the course of a prospective trial in such patients we determined azathioprine metabolites in erythrocytes, plasma, and urine as well as erythropoietin and hemoglobin levels in order to evaluate a potential interaction between these 2 drugs, possibly leading to anemia. Two specific high performance liquid chromatography (HPLC) methods for determination of azathioprine metabolites, both employing a mercurial cellulose resin for extraction, are presented. One method using a strong anion exchange column allows detection of 6-thioguanosine di- and triphosphate (thioguanine nucleotides) in red blood cells (RBC) with a sensitivity of 30 pmol/100 microliters RBC. 6-mercaptopurine (MP) and 6-thiouric acid (TUA) in plasma and urine were analyzed simultaneously by reversed-phase HPLC with a sensitivity of 5 ng/ml. The average (median values are given) steady state concentrations of thioguanine nucleotides in erythrocytes came to 267 pmol/100 microliters RBC (range 53-613) with and to 246 pmol/100 microliters RBC (range 39-629) without concomitant enalapril medication. Mean plasma concentrations of MP and TUA 3 hours after drug intake came to 14.8 +/- 9.9 ng/ml and 398 +/- 262 ng/ml, respectively, during enalapril comedication. Withdrawal of enalapril did not influence these metabolite levels coming to 15.3 +/- 9.1 and 451 +/- 253 after stopping enalapril treatment. Thioguanine nucleotides in RBCs were neither related to the dose of azathioprine given (r = -0.113, p > 0.05) nor to hemoglobin levels (r = 0.278, p > 0.05). However, azathioprine dose/kg body weight seemed to be related to hemoglobin concentration, with and without enalapril comedication. We conclude that enalapril therapy does not influence the measured azathioprine metabolites, the reported cases of anemia may rather be due to a pharmacodynamic interaction as shown by the significant increase in erythropoietin after withdrawal of enalapril. The assays described here are suitable to study the metabolism of azathioprine in patients with various diseases.
贫血在接受硫唑嘌呤免疫抑制治疗和依那普利治疗高血压的肾移植受者中经常被报道。在对这类患者进行的一项前瞻性试验过程中,我们测定了红细胞、血浆和尿液中的硫唑嘌呤代谢物以及促红细胞生成素和血红蛋白水平,以评估这两种药物之间可能导致贫血的潜在相互作用。本文介绍了两种采用汞纤维素树脂萃取法测定硫唑嘌呤代谢物的高效液相色谱(HPLC)方法。一种使用强阴离子交换柱的方法能够检测红细胞(RBC)中的6 - 硫鸟苷二磷酸和三磷酸(硫鸟嘌呤核苷酸),检测灵敏度为30 pmol/100微升红细胞。血浆和尿液中的6 - 巯基嘌呤(MP)和6 - 硫尿酸(TUA)通过反相HPLC同时分析,检测灵敏度为5 ng/ml。红细胞中硫鸟嘌呤核苷酸的平均(给出中位数)稳态浓度在联合使用依那普利时为267 pmol/100微升红细胞(范围53 - 613),不联合使用依那普利时为246 pmol/100微升红细胞(范围39 - 629)。在联合使用依那普利期间,服药3小时后MP和TUA的平均血浆浓度分别为14.8±9.9 ng/ml和398±262 ng/ml。停用依那普利后这些代谢物水平分别为15.3±9.1和451±253,停用依那普利并未影响这些水平。红细胞中的硫鸟嘌呤核苷酸既与所给硫唑嘌呤的剂量无关(r = -0.113,p>0.05),也与血红蛋白水平无关(r = 0.278,p>0.05)。然而,无论是否联合使用依那普利,硫唑嘌呤剂量/千克体重似乎与血红蛋白浓度有关。我们得出结论,依那普利治疗不影响所测定的硫唑嘌呤代谢物,报道的贫血病例可能更多是由于药效学相互作用,如停用依那普利后促红细胞生成素显著增加所示。本文所述的检测方法适用于研究各种疾病患者中硫唑嘌呤的代谢情况。