The mechanism of cyclosporine toxicity induced by clarithromycin

被引:47
|
作者
Spicer, ST
Liddle, C
Chapman, JR
Barclay, P
Nankivell, BJ
Thomas, P
OConnell, PJ
机构
[1] WESTMEAD HOSP,DEPT RENAL MED,WESTMEAD,NSW 2145,AUSTRALIA
[2] WESTMEAD HOSP,DEPT CLIN PHARMACOL,WESTMEAD,NSW 2145,AUSTRALIA
关键词
clarithromycin; cyclosporine A; cytochrome P450; CYP; 3A; erythromycin; breath test; acute renal failure; simvastatin; rhabdomyolysis;
D O I
10.1046/j.1365-2125.1997.54310.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aims Recently a number of case reports have described the interaction clarithromycin with cyclosporine A, resulting in cyclosporine toxicity. This interaction is presumed to take place via the hepatic cytochrome P450 enzyme system. Methods Following a case of cyclosporine toxicity and acute renal failure in a transplant patient started on clarithromycin, we investigated the effect of oral clarithromycin on the hepatic P450 system in five healthy normal male volunteers, by means of the erythromycin breath test. Results Cytochrome P4503A (CYP3A) activity was reduced in all subjects by a mean level of 26% following clarithromycin treatment. This would result in a significant reduction in cyclosporine clearance in patients receiving clarithromycin. Conclusions As clarithromycin was shown to inhibit CYP3A activity in all subjects tested, we recommend that a high degree of caution be exercised when clarithromycin is administered to patients receiving cyclosporine therapy or other drugs known to be eliminated by CYP3A-mediated metabolism.
引用
收藏
页码:194 / 196
页数:3
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