Lemahieu W P D, Maes B D, Verbeke K, Vanrenterghem Y
Division of Nephrology, University Hospitals Gasthuisberg, University of Leuven, Belgium.
Am J Transplant. 2004 Sep;4(9):1514-22. doi: 10.1111/j.1600-6143.2004.00539.x.
This study aimed to determine the impact of maintenance immunosuppressive therapy with cyclosporin A (CsA), tacrolimus (FK506) and sirolimus (Rapa) on the in vivo activity of both intestinal and hepatic cytochrome P450 3A4 (CYP3A4) and P-glycoprotein (PGP) in renal transplant patients. The activity of these four elimination pathways was measured by the recently validated intravenous (iv) and per oral (po)14C erythromycin breath and urine test. In addition, overall hepatic P450 activity was measured by the (13)C aminopyrin breath test. Three groups of stable renal transplant patients on maintenance therapy with corticosteroids (CS) and mycophenolate mofetil (MMF) plus either CsA or FK506 or Rapa were examined. A significant increase in intestinal CYP3A4 activity and a significant decrease in hepatic and intestinal PGP activity was seen in patients on CsA in comparison with those on FK506 or Rapa (p < 0.01). A similar analysis in six healthy volunteers at baseline and after intake of CsA, FK506 and Rapa confirmed the results seen in the patients. There was no difference in CYP3A4 and PGP activity in the patients taking either FK506 or Rapa and healthy controls. These data suggest that a different pattern of drug interactions might be expected in patients treated with CsA vs. FK506/Rapa.
本研究旨在确定肾移植患者中,使用环孢素A(CsA)、他克莫司(FK506)和西罗莫司(Rapa)进行维持性免疫抑制治疗对肠道和肝脏细胞色素P450 3A4(CYP3A4)及P-糖蛋白(PGP)体内活性的影响。这四条消除途径的活性通过最近验证的静脉注射(iv)和口服(po)14C红霉素呼气及尿液试验进行测定。此外,通过(13)C氨基比林呼气试验测定肝脏整体P450活性。对三组接受皮质类固醇(CS)和霉酚酸酯(MMF)维持治疗,同时加用CsA或FK506或Rapa的稳定肾移植患者进行了检查。与接受FK506或Rapa治疗的患者相比,接受CsA治疗的患者肠道CYP3A4活性显著增加,肝脏和肠道PGP活性显著降低(p < 0.01)。对六名健康志愿者在基线时以及摄入CsA、FK506和Rapa后的类似分析证实了在患者中观察到的结果。接受FK506或Rapa治疗的患者与健康对照在CYP3A4和PGP活性方面没有差异。这些数据表明,接受CsA治疗的患者与接受FK506/Rapa治疗的患者可能会出现不同模式的药物相互作用。