Yang C S, Tsai P J, Chen W Y, Kuo J S
Department of Education and Research, Taichung Veterans General Hospital, Taiwan.
J Chromatogr B Biomed Sci Appl. 2001 Mar 5;752(1):33-8. doi: 10.1016/s0378-4347(00)00510-7.
An assay for in vivo, continuous and automatic monitoring of extracellular malondialdehyde concentrations in anesthetized rat brain cortex was developed. This method involved the use of microdialysis perfusion, on-line derivatization and on-line high-performance liquid chromatographic analysis. Microdialysate from an implanted microdialysis probe was on-line reacted with thiobarbituric acid at 80 degrees C for 10 min prior to on-line collection and automatic injection into a HPLC system equipped with a fluorescence detector. This method gave a linear response between the concentrations of the malondialdehyde in the microdialysates and the TEP solution where the microdialysis probe was placed. This method was used to observe the increased extracellular malondialdehyde production following elevated extracellular glutamate levels, which were achieved by perfusion of L-trans-pyrrolidine-2,4-dicarboxylate, a competitive inhibitor of glutamate uptake transporter.
开发了一种用于在麻醉大鼠脑皮层中对细胞外丙二醛浓度进行体内连续自动监测的测定方法。该方法包括使用微透析灌注、在线衍生化和在线高效液相色谱分析。来自植入的微透析探针的微透析液在80℃下与硫代巴比妥酸在线反应10分钟,然后在线收集并自动注入配备荧光检测器的高效液相色谱系统。该方法在微透析液中丙二醛浓度与放置微透析探针的TEP溶液之间给出线性响应。该方法用于观察细胞外谷氨酸水平升高后细胞外丙二醛生成的增加,细胞外谷氨酸水平升高是通过灌注L-反式-脯氨酸-2,4-二羧酸(一种谷氨酸摄取转运体的竞争性抑制剂)实现的。