Yu X, Zhang B, Xing C, Sun B, Liu M, Zhang W, Gu M
First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Transplant Proc. 2008 Dec;40(10):3455-9. doi: 10.1016/j.transproceed.2008.06.089.
To investigate the differential effects of cyclosporine (CsA) and tacrolimus (TAC) on renal expression of P-glycoprotein (P-gp) in a cohort of kidney transplant recipients.
We enrolled 78 cadaveric kidney transplant recipients recurring basal immunosuppressive protocol with prednisone + mycophenolate mofetil + calcineurin inhibitor (CsA or TAC).
We performed a 3-year analysis of 60 patients. There was no difference in age, gender, or cold ischemic time between two groups, Serum creatinine, urine protein, and blood fat levels of the CsA group were significantly higher than the TAC group (P < .05), while the creatinine clearance was remarkably lower than the TAC group (P < .05). The incidence of tubular atrophy, arteriohyalinosis, and interstitial fibrosis and nephrotoxic lesions among the CsA group were higher than the TAC group, as well as the chronic allograft nephropathy (CAN) Banff score (P < .05). P-gp was predominantly present in the a tubular apical membrane, basal membrane, and cytoplasm. The intensity and extent of tubular staining score in the CsA group were lower compared with the TAC group (P < .01 and P < .05, respectively).
Less P-gp expression in the CsA group than the TAC group may be the molecular action pathway of the high incidence of CsA nephrotoxicity and CsA-induced CAN. This study perhaps unraveled a novel interpretation that the differences of CsA and TAC on long-term allograft survival were due to increases dynamic effects of CsA at the exposures employed in this study.
在一组肾移植受者中研究环孢素(CsA)和他克莫司(TAC)对肾脏P-糖蛋白(P-gp)表达的不同影响。
我们纳入了78例接受泼尼松+霉酚酸酯+钙调神经磷酸酶抑制剂(CsA或TAC)基础免疫抑制方案的尸体肾移植受者。
我们对60例患者进行了为期3年的分析。两组在年龄、性别或冷缺血时间上无差异,CsA组的血清肌酐、尿蛋白和血脂水平显著高于TAC组(P < 0.05),而肌酐清除率显著低于TAC组(P < 0.05)。CsA组的肾小管萎缩、动脉玻璃样变、间质纤维化和肾毒性病变的发生率高于TAC组,慢性移植肾肾病(CAN)的Banff评分也高于TAC组(P < 0.05)。P-gp主要存在于肾小管顶端膜、基底膜和细胞质中。CsA组肾小管染色评分的强度和范围低于TAC组(分别为P < 0.01和P < 0.05)。
CsA组P-gp表达低于TAC组可能是CsA肾毒性和CsA诱导的CAN高发的分子作用途径。本研究可能揭示了一种新的解释,即CsA和TAC对长期移植肾存活的差异是由于本研究中使用的CsA暴露增加了动态效应。