Zhang Jing, Jaquins-Gerstl Andrea, Nesbitt Kathryn M, Rutan Sarah C, Michael Adrian C, Weber Stephen G
Department of Chemistry, University of Pittsburgh , Pittsburgh, Pennsylvania 15260, United States.
Anal Chem. 2013 Oct 15;85(20):9889-97. doi: 10.1021/ac4023605. Epub 2013 Sep 24.
Online monitoring of serotonin in striatal dialysate from freely moving rats was carried out for more than 16 h at 1 min time resolution using microdialysis coupled online to a capillary HPLC system operating at about 500 bar and 50 °C. Several aspects of the system were optimized toward robust, in vivo online measurements. A two-loop, eight-port rotary injection valve demonstrated better consistency of continuous injections than the more commonly used two-loop, 10-port valve. A six-port loop injector for introducing stimulating solutions (stimulus injector) was placed in-line between the syringe pump and microdialysis probe. We minimized solute dispersion by using capillary tubing (75 μm inside diameter, 70 cm long) for the probe inlet and outlet. In vitro assessment of concentration dispersion during transport with a 30 s time resolution showed that the dispersion standard deviation for serotonin was well within the desired system temporal resolution. Each 30 or 60 s measurement reflects the integral of the true time response over the measurement time. We have accounted for this mathematically in determining the concentration dispersion during transport. The delay time between a concentration change at the probe and its detection is 7 min. The timing of injections from the stimulus injector and the cycle time for the HPLC monitoring of the flow stream were controlled. The electrochemical detector contained a 13 μm spacer to minimize detector dead volume. During in vivo experiments, retention time and separation efficiency were stable and reproducible. There was no statistically significant change over 5.5 h in the electrochemical detector sensitivity factor for serotonin. Dialysate serotonin concentrations change significantly in response to a 120 mM K(+) stimulus. Release of serotonin evoked by a 10 min, 120 mM K(+) stimulation, but not for other K(+) stimuli, exhibited a reproducible, oscillating profile of dialysate serotonin concentration versus time. Infusion of fluoxetine, a serotonin uptake inhibitor, increased dialysate serotonin concentrations and stimulated release magnitude. Transient serotonin increases were observed in response to the stress associated with unexpected handling. This system is simple, efficient, reliable, and suitable for the study of serotonin neurochemistry associated with emotion and behavior.
使用与在约500巴和50℃下运行的毛细管高效液相色谱系统在线耦合的微透析技术,以1分钟的时间分辨率对自由活动大鼠纹状体透析液中的血清素进行了超过16小时的在线监测。针对稳健的体内在线测量对系统的几个方面进行了优化。与更常用的双环十通阀相比,双环八通旋转进样阀显示出连续进样更好的一致性。用于引入刺激溶液的六通环进样器(刺激进样器)在线放置在注射泵和微透析探头之间。我们通过使用内径75μm、长70cm的毛细管作为探头入口和出口来最小化溶质扩散。以30秒的时间分辨率对传输过程中的浓度扩散进行体外评估表明,血清素的扩散标准偏差完全在所需的系统时间分辨率范围内。每次30或60秒的测量反映了测量时间内真实时间响应的积分。我们在确定传输过程中的浓度扩散时已经从数学上考虑了这一点。探头处浓度变化与其检测之间的延迟时间为7分钟。控制了刺激进样器的进样时间和高效液相色谱对流动相监测的循环时间。电化学检测器包含一个13μm的间隔物以最小化检测器死体积。在体内实验期间,保留时间和分离效率稳定且可重复。血清素的电化学检测器灵敏度因子在5.5小时内没有统计学上的显著变化。透析液血清素浓度对120mM K(+)刺激有显著变化。10分钟、120mM K(+)刺激引起的血清素释放,但其他K(+)刺激则不然,呈现出透析液血清素浓度随时间变化的可重复振荡曲线。血清素摄取抑制剂氟西汀的输注增加了透析液血清素浓度并刺激了释放幅度。观察到因意外处理相关的应激而导致血清素短暂增加。该系统简单、高效、可靠,适用于研究与情绪和行为相关的血清素神经化学。