Xin Hua-Wen, Fischer Christine, Schwab Matthias, Klotz Ulrich
Dr. Margarete Fischer-Bosch Institute of Clinical Pharmacology, Auerbachstrasse 112, D-70376, Stuttgart, Germany.
Eur J Clin Pharmacol. 2005 Jul;61(5-6):395-8. doi: 10.1007/s00228-005-0950-5. Epub 2005 Jun 11.
The present study was undertaken to investigate the possible effects of various agents on thiopurine methyltransferase (TPMT) activity in red blood cells (RBCs) from patients with chronic inflammatory bowel disease (IBD).
In three groups of patients with very high, normal and intermediate TPMT activity (each n=6), the inhibitory potential of furosemide, piretanide, azathioprine (AZA) and testosterone was assessed by ex vivo measurements of TPMT activity in RBCs. From individual concentration-response curves, IC50 values have been determined.
Independent of the basal TPMT activity, lowest IC50 values were calculated for furosemide (15-19 microM), followed by testosterone (30-72 microM), piretanide (300-313 microM) and AZA (430-532 microM). Compared with reported plasma concentration achieved during treatment, only furosemide would have the potential to inhibit TPMT also in vivo, whereas the IC50 values of the other agents are far above the corresponding plasma levels.
Our ex vivo study revealed that only furosemide has the potential to inhibit TPMT activity in patients with IBD. This possibility should be taken into consideration if the diuretic and AZA or 6-mercaptopurine are coadministered. However, the extrapolation to the clinical setting remains open.
本研究旨在探讨多种药物对慢性炎症性肠病(IBD)患者红细胞(RBC)中硫嘌呤甲基转移酶(TPMT)活性的可能影响。
在三组TPMT活性分别为非常高、正常和中等的患者(每组n = 6)中,通过体外测量RBC中的TPMT活性来评估呋塞米、吡咯他尼、硫唑嘌呤(AZA)和睾酮的抑制潜力。根据个体浓度 - 反应曲线,确定了IC50值。
无论基础TPMT活性如何,计算得出呋塞米的IC50值最低(15 - 19 microM),其次是睾酮(30 - 72 microM)、吡咯他尼(300 - 313 microM)和AZA(430 - 532 microM)。与治疗期间报道的血浆浓度相比,只有呋塞米有可能在体内也抑制TPMT,而其他药物的IC50值远高于相应的血浆水平。
我们的体外研究表明,只有呋塞米有可能抑制IBD患者的TPMT活性。如果同时使用利尿剂和AZA或6 - 巯基嘌呤,应考虑这种可能性。然而,将其外推至临床情况仍未明确。