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肝移植受者血液和尿液中环孢素的代谢物模式。I. 环孢素代谢物与肾毒性的关联。

Ciclosporin metabolite pattern in blood and urine of liver graft recipients. I. Association of ciclosporin metabolites with nephrotoxicity.

作者信息

Christians U, Kohlhaw K, Budniak J, Bleck J S, Schottmann R, Schlitt H J, Almeida V M, Deters M, Wonigeit K, Pichlmayr R

机构信息

Institut für Allgemeine Pharmakologie, Medizinische Hochschule Hannover, FRG.

出版信息

Eur J Clin Pharmacol. 1991;41(4):285-90. doi: 10.1007/BF00314953.

DOI:10.1007/BF00314953
PMID:1804640
Abstract

Blood ciclosporin (Cs) metabolite pattern in 58 liver grafted patients was routinely monitored by HPLC from the first Cs dose after transplantation until discharge from hospital. Eighteen patients with normal kidney function were allocated to Group I and 14 patients in Group II suffered Cs nephrotoxicity during their clinical course. There were no significant differences between both groups in blood Cs level, kidney function before transplantation, liver function or co-administration of other potentially nephrotoxic drugs. A correlation matrix involving both groups showed a significant correlation between the blood concentration of metabolite M1c9 and serum creatinine and urea, and an inverse correlation with creatinine clearance. During a nephrotoxic episode the blood concentrations of metabolites M1c9 and M1A were significantly elevated in patients in Group II. Analysis of the time course revealed significantly higher blood levels of M19 and M1c9 in Group II patients compared with those in Group I for the first 10 days after transplantation. Serum creatinine and urea concentrations remained significantly elevated, the creatinine clearance being significantly reduced throughout the period of observation. The elevated blood concentrations of ciclosporin metabolites M1c9 and M19 during nephrotoxic episodes suggest that these metabolites are associated with ciclosporin nephrotoxicity. It could not be decided if the elevated metabolite concentrations were the result of and/or the reason for impaired kidney function.

摘要

从移植后首次给予环孢素(Cs)剂量直至出院,通过高效液相色谱法(HPLC)对58例肝移植患者的血液中环孢素代谢物模式进行常规监测。18例肾功能正常的患者被分配到I组,II组中有14例患者在临床过程中出现Cs肾毒性。两组在血液Cs水平、移植前肾功能、肝功能或其他潜在肾毒性药物的联合使用方面均无显著差异。涉及两组的相关矩阵显示,代谢物M1c9的血药浓度与血清肌酐和尿素之间存在显著相关性,与肌酐清除率呈负相关。在肾毒性发作期间,II组患者血液中的代谢物M1c9和M1A浓度显著升高。时间进程分析显示,与I组相比,II组患者在移植后的前10天血液中M19和M1c9水平显著更高。在整个观察期内,血清肌酐和尿素浓度仍显著升高,肌酐清除率显著降低。肾毒性发作期间环孢素代谢物M1c9和M19的血药浓度升高表明,这些代谢物与环孢素肾毒性有关。目前尚无法确定代谢物浓度升高是肾功能受损的结果还是原因。

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1
Ciclosporin metabolite pattern in blood and urine of liver graft recipients. I. Association of ciclosporin metabolites with nephrotoxicity.肝移植受者血液和尿液中环孢素的代谢物模式。I. 环孢素代谢物与肾毒性的关联。
Eur J Clin Pharmacol. 1991;41(4):285-90. doi: 10.1007/BF00314953.
2
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Eur J Clin Pharmacol. 1991;41(4):291-6. doi: 10.1007/BF00314954.
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引用本文的文献

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本文引用的文献

1
Disposition of cyclosporine in several animal species and man. I. Structural elucidation of its metabolites.环孢素在几种动物物种和人类中的处置。I. 其代谢产物的结构解析。
Drug Metab Dispos. 1984 Jan-Feb;12(1):120-6.
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Biotransformation and distribution in blood of cyclosporine and its metabolites.环孢素及其代谢产物在血液中的生物转化与分布。
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Measurement of cyclosporin A and of four metabolites in whole blood by high-performance liquid chromatography.通过高效液相色谱法测定全血中环孢素A及四种代谢物的含量。
肝移植后免疫调节治疗中第三方多能成体祖细胞的安全性和可行性:一项 I 期研究(MISOT-I)。
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Effect of CYP3A and ABCB1 single nucleotide polymorphisms on the pharmacokinetics and pharmacodynamics of calcineurin inhibitors: Part II.CYP3A 和 ABCB1 单核苷酸多态性对钙调神经磷酸酶抑制剂的药代动力学和药效学的影响:第二部分。
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Conversion of cardiac and liver transplant recipients from HPLC and FPIA (polyclonal) to an FPIA (monoclonal) technique for measurement of blood cyclosporin A.心脏和肝脏移植受者从采用高效液相色谱法(HPLC)和荧光偏振免疫分析法(FPIA,多克隆)转换为采用荧光偏振免疫分析法(FPIA,单克隆)来测定血中环孢素A。
J Clin Lab Anal. 1998;12(6):337-42. doi: 10.1002/(sici)1098-2825(1998)12:6<337::aid-jcla2>3.0.co;2-d.
7
[Effect of diltiazem on concentration of cyclosporin metabolites in Sandimmune and Neoral treated kidney transplant patients].[地尔硫䓬对接受山地明和新山地明治疗的肾移植患者中环孢素代谢物浓度的影响]
Med Klin (Munich). 1997 Oct 15;92(10):589-96. doi: 10.1007/BF03044784.
8
The use of therapeutic drug monitoring to optimise immunosuppressive therapy.使用治疗药物监测来优化免疫抑制治疗。
Clin Pharmacokinet. 1996 Feb;30(2):107-40. doi: 10.2165/00003088-199630020-00003.
9
Cyclosporin clinical pharmacokinetics.环孢素的临床药代动力学。
Clin Pharmacokinet. 1993 Jun;24(6):472-95. doi: 10.2165/00003088-199324060-00004.
J Chromatogr. 1987 Jan 23;413:121-9. doi: 10.1016/0378-4347(87)80219-0.
4
The covalent binding of cyclosporin A to rat liver macromolecules in vivo and in vitro: the role of cytochrome P-450.环孢素A在体内和体外与大鼠肝脏大分子的共价结合:细胞色素P-450的作用。
Toxicology. 1987 Dec 14;47(3):277-84. doi: 10.1016/0300-483x(87)90057-6.
5
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6
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8
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Liquid-chromatographic measurement of cyclosporin A and its metabolites in blood, bile, and urine.血液、胆汁和尿液中环孢素A及其代谢产物的液相色谱测定
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