Aeschlimann C, Cerny T, Küpfer A
Department of Clinical Pharmacology, University of Berne, Switzerland.
Drug Metab Dispos. 1996 Dec;24(12):1336-9.
The clinical application of ifosfamide is hampered by a central nervous side effect, the so-called ifosfamide encephalopathy. Methylene blue is effective in prophylaxis and reversal of this side effect. In the present study, the in vitro inhibition of (mono)amine oxidases by methylene blue is demonstrated in two different experimental systems. The results provide an explanation for the preventive action of methylene blue in ifosfamide neurotoxicity, because the generation of chloroacetaldehyde (a potential neurotoxin of ifosfamide metabolism) is prevented in liver mitochondria and extrahepatic tissues. Generation of alkylating metabolites was also studied in rat liver perfusions, and methylene blue did not show any inhibition of ifosfamide activation. From these data, we conclude that the clinical effectiveness of methylene blue in treatment and prevention of ifosfamide encephalopathy might be based on inhibition of (mono)amine oxidases. Hepatic bioactivation of ifosfamide is not influenced by methylene blue.
异环磷酰胺的临床应用受到一种中枢神经副作用(即所谓的异环磷酰胺脑病)的阻碍。亚甲蓝对这种副作用的预防和逆转有效。在本研究中,在两种不同的实验系统中证明了亚甲蓝对(单)胺氧化酶的体外抑制作用。这些结果为亚甲蓝对异环磷酰胺神经毒性的预防作用提供了解释,因为在肝线粒体和肝外组织中可防止氯乙醛(异环磷酰胺代谢的一种潜在神经毒素)的生成。在大鼠肝脏灌注中也研究了烷基化代谢产物的生成,亚甲蓝未显示对异环磷酰胺活化有任何抑制作用。根据这些数据,我们得出结论,亚甲蓝在治疗和预防异环磷酰胺脑病方面的临床有效性可能基于对(单)胺氧化酶的抑制作用。亚甲蓝不影响异环磷酰胺的肝脏生物活化。