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Determination of cyanidin 3-glucoside in rat brain, liver and kidneys by UPLC/MS-MS and its application to a short-term pharmacokinetic study

机译:UPLC / MS-MS测定大鼠脑,肝和肾中花色素3-葡萄糖苷的含量及其在短期药代动力学研究中的应用

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摘要

Anthocyanins exert neuroprotection in various in vitro and in vivo experimental models. However, no details regarding their brain-related pharmacokinetics are so far available to support claims about their direct neuronal bioactivity as well as to design proper formulations of anthocyanin-based products. To gather this missing piece of knowledge, we intravenously administered a bolus of 668 nmol cyanidin 3-glucoside (C3G) in anaesthetized Wistar rats and shortly after (15 s to 20 min) we collected blood, brain, liver, kidneys and urine samples. Extracts thereof were analysed for C3G and its expected metabolites using UPLC/MS-MS. The data enabled to calculate a set of pharmacokinetics parameters. The main finding was the distinctive, rapid distribution of C3G in the brain, with an apparently constant plasma/brain ratio in the physiologically relevant plasma concentration range (19–355 nM). This is the first report that accurately determines the distribution pattern of C3G in the brain, paving the way to the rational design of future tests of neuroprotection by C3G in animal models and humans.
机译:花色苷在各种体外和体内实验模型中发挥神经保护作用。但是,到目前为止,尚无关于其与大脑有关的药代动力学的细节可用于支持有关其直接神经元生物活性以及设计基于花色苷的产品的适当配方的主张。为了收集这些缺失的知识,我们在麻醉的Wistar大鼠中静脉内注射668 nmol氰苷3-葡糖苷(C3G)推注,并在不久(15 s至20 min)后收集了血液,脑,肝,肾和尿液样本。使用UPLC / MS-MS分析了其提取物中的C3G及其预期代谢产物。该数据能够计算一组药代动力学参数。主要发现是脑中C3G的独特而快速的分布,在生理相关的血浆浓度范围(19-355 nM)中,血浆/脑比例明显恒定。这是第一份准确确定C3G在大脑中的分布方式的报告,为合理设计C3G在动物模型和人类中进行神经保护的未来测试铺平了道路。

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