氯氮平- n -氧化物给药后豚鼠和人体内氯氮平的快速形成。

M W Jann, Y W Lam, W H Chang
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引用次数: 0

摘要

氯氮平及其代谢物氯氮平n -氧化物(0.5 mg/kg)腹腔注射豚鼠。氯氮平- n -氧化物给药后,血浆、肝脏、额叶皮质和尾状核中检测到显著量的氯氮平。n -氧化物给药后2小时血浆中氯氮平的含量约为氯氮平注射后氯氮平含量的40%。肝、额叶皮质和尾状核组织氯氮平浓度高于血浆浓度。氯氮平在肝脏中的浓度几乎相等。n -氧化物注射后的氯氮平浓度比给药后的氯氮平在额叶皮层和尾状核中的浓度低约40-50%。给一名精神分裂症患者服用单剂量氯氮平- n -氧化物。n -氧化物给药后检测氯氮平血药浓度。本研究表明氯氮平是由其n -氧化物代谢物形成的,氯氮平和氯氮平- n -氧化物存在可逆的代谢途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rapid formation of clozapine in guinea-pigs and man following clozapine-N-oxide administration.

Clozapine and its metabolite clozapine-N-oxide (0.5 mg/kg) were administered intraperitoneally to guinea-pigs. Significant amounts of clozapine were detected in plasma, liver, frontal cortex and caudate after clozapine-N-oxide administration. The amount of clozapine detected in plasma two hours post-administration of N-oxide was approximately 40% of the amount of clozapine after clozapine injection. Tissue concentrations of clozapine in liver, frontal cortex and caudate were greater than plasma concentrations. Clozapine concentrations were almost equivalent in the liver. Clozapine concentrations after N-oxide injection were approximately 40-50% lower compared to clozapine concentrations after clozapine administration in the frontal cortex and caudate. A single dose of clozapine-N-oxide was given to a schizophrenic patient. Clozapine plasma concentrations were detected after N-oxide administration. This study shows that clozapine is formed from its N-oxide metabolite and that a reversible metabolic pathway exists for clozapine and clozapine-N-oxide.

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