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在卡马西平-乙醇相互作用过程中大鼠脑纹状体中萨索林醇的气-液色谱测定

Gas-liquid chromatographic determination of salsolinol in the striatum of rat brain during the calcium carbimide--ethanol interaction.

作者信息

Brien J F, Andrews P J, Loomis C W, Page J A

出版信息

Can J Physiol Pharmacol. 1983 Jun;61(6):632-40. doi: 10.1139/y83-097.

Abstract

An assay has been developed for the measurement of salsolinol in brain tissue that involves tissue homogenization in dilute hydrochloric acid, purification of the supernatant by cation-exchange chromatography, derivatization of the eluate with heptafluorobutyric anhydride, and analysis by gas-liquid chromatography with electron capture detection using p-tyramine as the internal standard. The lower limit of quantitative sensitivity, using aqueous standards, is 2.5 ng salsolinol per brain sample. This assay was used to study salsolinol formation in rat brain during the calcium carbimide-ethanol interaction. Rats were administered ethanol (1.0 g/kg) by oral intubation 3 h after intraperitoneal administration of calcium carbimide (7.0 mg/kg). Salsolinol was measured in the striatum over a 270-min period after ethanol administration. Salsolinol concentration appeared to be maximal (275 ng/g) at 90 min and then declined with an apparent elimination half-life of 39.8 min.

摘要

已开发出一种用于测量脑组织中胡豆碱的分析方法,该方法包括在稀盐酸中对组织进行匀浆、通过阳离子交换色谱法纯化上清液、用七氟丁酸酐对洗脱液进行衍生化,以及使用对酪胺作为内标通过气液色谱法和电子捕获检测进行分析。使用水性标准品时,定量灵敏度的下限为每个脑样本2.5 ng胡豆碱。该分析方法用于研究在卡马咪嗪 - 乙醇相互作用期间大鼠脑中胡豆碱的形成。在腹腔注射卡马咪嗪(7.0 mg/kg)3小时后,通过口服灌胃给大鼠施用乙醇(1.0 g/kg)。在乙醇给药后的270分钟内测量纹状体中的胡豆碱。胡豆碱浓度在90分钟时似乎达到最大值(275 ng/g),然后下降,表观消除半衰期为39.8分钟。

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