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新型设计药物 3-氟甲卡西酮的 I 期代谢的兔肝切片研究。

Studies on the phase I metabolism of the new designer drug 3-fluoromethcathinone using rabbit liver slices.

机构信息

Institute of Legal Medicine, Heinrich-Heine University, Duesseldorf, Germany.

出版信息

Int J Legal Med. 2012 Mar;126(2):231-40. doi: 10.1007/s00414-011-0601-6. Epub 2011 Jul 23.

Abstract

The metabolism of the novel designer drug 3-fluoromethcathinone (3-FMC), sold as "legal highs", was investigated in vitro via cryopreserved rabbit liver slices. The pharmacological properties and toxicological effects of 3-FMC and its metabolites are not known yet. It can be assumed that 3-FMC will cause effects similar to 4-methylmethcathinone (mephedrone) and methcathinone. For the metabolism studies, pretests were performed with rabbit liver slices incubated with kavain to evaluate optimal conditions. Finally, six known metabolites of kavain were revealed and therefore sufficient information about the suitability of the enzyme system of the rabbit liver slices was obtained. Under optimized conditions, 3-FMC was added to Krebs-Henseleit buffer, pH 7.4 containing NADPH and bicarbonate and incubated with a single rabbit liver slice at 37°C. The metabolism was monitored at 5, 30 and 180 min, respectively. The metabolites formed via the former cryopreserved rabbit liver slices were examined by LC/MS-TOF. Metabolites were identified by their exact masses and isotopic patterns. 3-Fluorocathinone, 3-fluorocathinone-imine, hydroxy-3-fluoromethcathinone and 3-fluoromethcathinone-diol were formed as the main metabolites.

摘要

新型设计药物 3-氟甲卡西酮(3-FMC),作为“合法兴奋剂”出售,其代谢在体外通过冷冻保存的兔肝切片进行了研究。3-FMC 及其代谢物的药理性质和毒理学效应尚不清楚。可以假设 3-FMC 将引起类似于 4-甲基甲卡西酮(苯丙胺)和甲卡西酮的作用。为了进行代谢研究,用兔肝切片孵育卡瓦宁进行了预试验,以评估最佳条件。最终揭示了六个已知的卡瓦宁代谢物,因此获得了关于兔肝切片酶系统适用性的足够信息。在优化条件下,将 3-FMC 添加到 pH 7.4 的 Krebs-Henseleit 缓冲液中,含有 NADPH 和碳酸氢盐,并在 37°C 下与单个兔肝切片一起孵育。分别在 5、30 和 180 分钟监测代谢情况。通过以前的冷冻保存的兔肝切片形成的代谢物通过 LC/MS-TOF 进行检查。通过其精确质量和同位素模式来鉴定代谢物。形成了主要代谢物 3-氟卡西酮、3-氟卡西酮亚胺、羟基-3-氟甲卡西酮和 3-氟甲卡西酮二醇。

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