Department of Pharmaceutical Sciences and Center for Vascular Drug Research, School of Pharmacy, Texas Tech University Health Sciences Center, 1300 Coulter Dr, Amarillo, TX 79106, USA.
Neurochem Res. 2011 Jan;36(1):109-16. doi: 10.1007/s11064-010-0276-2. Epub 2010 Sep 28.
The current study used measurements of metabolites and markers of membrane integrity to determine the most suitable time point for microdialysis experiments following probe implantation. Leakage of Evans blue and sodium fluorescein indicated increased BBB permeability only immediately (15 min), but not 1.5 and 24 h following probe implantation. Acute implantation decreased glucose and lactate levels relative to the levels after 24 h (to 13-37% and 25-60%, respectively). No change in extracellular levels of glutamate or glycerol was seen. In comparison to acute probe implantation, the pattern of damage under brain ischemia (middle cerebral artery occlusion) differed: While glucose levels dropped, lactate levels rose after ischemia, and glutamate (tenfold) and glycerol (eightfold) increased sharply. In conclusion, acute implantation of a microdialysis probe causes transient depression of the energy metabolites, glucose and lactate, likely due to injury-induced hypermetabolism. However, no massive tissue damage or severe ischemic conditions around the probe occur.
本研究使用代谢物和膜完整性标志物的测量来确定在探针植入后进行微透析实验的最合适时间点。伊文思蓝和荧光素钠的渗漏表明 BBB 通透性仅在即刻(15 分钟)增加,而不是在探针植入后 1.5 和 24 小时。急性植入与 24 小时后相比,葡萄糖和乳酸水平下降(分别下降到 13-37%和 25-60%)。细胞外谷氨酸或甘油水平没有变化。与急性探针植入相比,脑缺血(大脑中动脉闭塞)下的损伤模式不同:葡萄糖水平下降,缺血后乳酸水平升高,谷氨酸(十倍)和甘油(八倍)急剧增加。总之,微透析探针的急性植入会导致能量代谢物葡萄糖和乳酸的短暂抑制,这可能是由于损伤诱导的代谢亢进所致。然而,探针周围没有发生大量的组织损伤或严重的缺血情况。