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氯氮平在大鼠体内的分布:在肺中的定位

Distribution of clozapine in the rat: localization in lung.

作者信息

Gardiner T H, Lewis J M, Shore P A

出版信息

J Pharmacol Exp Ther. 1978 Jul;206(1):151-7.

PMID:660545
Abstract

To determine the distribution of the antipsychotic agent, clozapin (CLZ), a fluorometric procedure for its estimation was devised, and the drug was measured in various tissues of rats after i.p. injection (20 mg/kg). In a 24-hour urine collection, less than 1% injected drug was found. After 1 hour, CLZ concentrations were greatest in lung, spleen, liver and brain (16-64 microgram/g). After 6 hours, CLZ levels in lung remained at 52 microgram/g, whereas concentrations in all other tissues declined to less than 7 microgram/g. When rat lung slices were incubated (O2, 37 degrees C) in CLZ solution (20 microgram/ml), the drug was taken up by the tissue against a concentration gradient, attaining a maximum tissue/medium ratio of 97 after 4 hours. When the concentration of CLZ was raised from 2 to 200 microgram/ml the 1-hour tissue/medium ratio declined from 89 to 21. Chlordiazepoxide, amphetamine and morphine depressed the 1-hour tissue/medium ratio of CLZ by 34 to 50%. CLZ uptake was also decreased 19% by anaerobic conditions and 25% by the presence of 2,4-dinitrophenol. The results suggest that the lung is a site of (active) transport and accumulation for CLZ and perhaps certain other basic drugs.

摘要

为了确定抗精神病药物氯氮平(CLZ)的分布情况,设计了一种用于其测定的荧光测定法,并在大鼠腹腔注射(20mg/kg)后测定了其在大鼠各种组织中的含量。在收集24小时尿液时,发现注射药物的排出量不到1%。1小时后,肺、脾、肝和脑中的CLZ浓度最高(16 - 64微克/克)。6小时后,肺中的CLZ水平保持在52微克/克,而所有其他组织中的浓度降至7微克/克以下。当将大鼠肺切片在CLZ溶液(20微克/毫升)中于37℃、有氧条件下孵育时,药物逆浓度梯度被组织摄取,4小时后组织/培养基的最大比值达到97。当CLZ的浓度从2微克/毫升提高到200微克/毫升时,1小时的组织/培养基比值从89降至21。氯氮卓、苯丙胺和吗啡使CLZ的1小时组织/培养基比值降低了34%至50%。无氧条件使CLZ的摄取量降低了19%,2,4 - 二硝基苯酚的存在使其降低了25%。结果表明,肺是CLZ以及可能某些其他碱性药物的(主动)转运和蓄积部位。

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