Central Laboratory, Changchun Normal University, Changchun, China.
Changchun Center of Mass Spectrometry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, China.
J Sep Sci. 2017 Apr;40(8):1773-1783. doi: 10.1002/jssc.201700054. Epub 2017 Mar 17.
Stroke is one of the most common diseases worldwide. Lactate dehydrogenase inhibitors are widely used in the treatment of ischemic stroke, with natural products considered a promising source of lactate dehydrogenase inhibitors. In this study, ultrafiltration liquid chromatography coupled with mass spectrometry was used for the screening and identification of lactate dehydrogenase inhibitors from Poria cocos. Five lactate dehydrogenase inhibitors were selected: dehydropachymic acid, pachymic acid, dehydrotrametenolic acid, trametenolic acid, and eburicoic acid. The inhibitors were extracted and isolated with purities of 96.75, 98.15, 97.25, 95.46, and 94.88%, respectively, by using a new "hyphenated" strategy of microwave-assisted extraction coupled with counter-current chromatography and centrifugal partition chromatography by a two-phase solvent system of n-hexane/ethyl acetate/ethanol/water at the volume ratio 0.965:1.000:0.936:0.826 v/v/v/v. The bioactivity of the isolated compounds was assessed using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay in PC12 cells. The results also showed that the hyphenated technique of microwave-assisted extraction coupled with counter-current chromatography and centrifugal partition chromatography was an efficient method for the continuous extraction and online isolation of chemical constituents from medicinal herbs. Furthermore, the research route based on the activity screening, extraction, separation, and activity verification of the compounds offered advantages of efficiency, orientation, and objectivity.
中风是全球最常见的疾病之一。乳酸脱氢酶抑制剂广泛用于治疗缺血性中风,天然产物被认为是乳酸脱氢酶抑制剂的有前途的来源。在这项研究中,超滤液相色谱与质谱联用技术用于从茯苓中筛选和鉴定乳酸脱氢酶抑制剂。选择了五种乳酸脱氢酶抑制剂:脱水巴戟酸、巴戟酸、去氢千里光萜烯酸、千里光萜烯酸和伊布瑞考酸。抑制剂通过使用新型“连接”策略,即微波辅助提取与逆流色谱和两相溶剂系统(正己烷/乙酸乙酯/乙醇/水的体积比为 0.965:1.000:0.936:0.826v/v/v/v)的离心分配色谱相结合进行提取和分离,纯度分别达到 96.75%、98.15%、97.25%、95.46%和 94.88%。采用 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐法在 PC12 细胞中评估分离化合物的生物活性。结果还表明,微波辅助提取与逆流色谱和离心分配色谱相结合的连接技术是一种从草药中连续提取和在线分离化学成分的有效方法。此外,基于化合物的活性筛选、提取、分离和活性验证的研究途径具有高效、定向和客观的优点。