Naito Takafumi, Shinno Kazuko, Maeda Toshio, Kagawa Yoshiyuki, Hashimoto Hisakuni, Otsuka Atsushi, Takayama Tatsuya, Ushiyama Tomomi, Suzuki Kazuo, Ozono Seiichiro
Division of Hospital Pharmacy, Hamamatsu University School of Medicine, 1-20-1 Handa-yama, Hamamatsu 431-3192, Japan.
Biol Pharm Bull. 2006 Feb;29(2):275-80. doi: 10.1248/bpb.29.275.
Mycophenolic acid (MPA), the active metabolite of mycophenolate mofetil (MMF) has been introduced into renal transplant immunosuppressant protocols in combination with calcineurin inhibitors (CNIs) and steroids. This study compared the pharmacokinetic profiles of MPA and its major metabolite MPA glucuronide (MPAG) in combination with tacrolimus (TAC) or cyclosporine (CyA) during the maintenance period (>6 months) following renal transplantation. There was no difference between TAC and CyA-treated groups in MPA plasma concentration before drug administration (C(0)). MPA C(0) in TAC and CyA-treated patients did not differ from that in patients who were not treated with a CNI. In patients treated with a CNI, MPAG C(0) was significantly greater in those treated with CyA compared with TAC. The MPAG/MPA ratio in CyA-treated patients was significantly greater than that in the TAC-treated group. We observed that C(0) of MPA was negatively correlated with that of TAC and CyA. Positive correlation between MPA C(0), MPAG C(0) and serum creatinine was stronger in patients treated with CyA compared with TAC. Our study suggests that CyA, but not TAC, inhibits enterohepatic circulation of MPAG as a secondary excretion pathway, and that renal function makes a major contribution to elimination of MPA and MPAG. We indicate that it may be necessary to estimate biliary excretion of MPAG to avoid the risk of intestinal injury in patients receiving combination therapy with TAC during the maintenance period.
霉酚酸(MPA)是霉酚酸酯(MMF)的活性代谢产物,已被引入肾移植免疫抑制方案中,与钙调神经磷酸酶抑制剂(CNIs)和类固醇联合使用。本研究比较了肾移植维持期(>6个月)联合使用他克莫司(TAC)或环孢素(CyA)时MPA及其主要代谢产物MPA葡萄糖醛酸苷(MPAG)的药代动力学特征。给药前(C(0)),TAC组和CyA组患者的MPA血浆浓度无差异。TAC组和CyA组患者的MPA C(0)与未接受CNI治疗的患者无差异。在接受CNI治疗的患者中,CyA治疗组的MPAG C(0)显著高于TAC治疗组。CyA治疗组的MPAG/MPA比值显著高于TAC治疗组。我们观察到MPA的C(0)与TAC和CyA的C(0)呈负相关。与TAC治疗的患者相比,CyA治疗的患者中MPA C(0)、MPAG C(0)与血清肌酐之间的正相关性更强。我们的研究表明,CyA而非TAC抑制MPAG作为次要排泄途径的肠肝循环,并且肾功能对MPA和MPAG的消除起主要作用。我们指出,在维持期接受TAC联合治疗的患者中,可能有必要评估MPAG的胆汁排泄,以避免肠道损伤风险。