Globus M Y, Busto R, Lin B, Schnippering H, Ginsberg M D
Department of Neurology, University of Miami School of Medicine, Florida 33101, USA.
J Neurochem. 1995 Sep;65(3):1250-6. doi: 10.1046/j.1471-4159.1995.65031250.x.
To obtain direct evidence of oxygen radical activity in the course of cerebral ischemia under different intraischemic temperatures, we used a method based on the chemical trapping of hydroxyl radical in the form of the stable adducts 2,3- and 2,5-dihydroxybenzoic acid (DHBA) following salicylate administration. Wistar rats were subjected to 20 min of global forebrain ischemia by two-vessel occlusion plus systemic hypotension (50 mm Hg). Intraischemic striatal temperature was maintained as normothermic (37 degrees C), hypothermic (30 degrees C), or hyperthermic (39 degrees C) but was held at 37 degrees C before and following ischemia. Salicylate was administered either systemically (200 mg/kg, i.p.) or by continuous infusion (5 mM) through a microdialysis probe implanted in the striatum. Striatal extracellular fluid was sampled at regular intervals before, during, and after ischemia, and levels of 2,3- and 2,5-DHBA were assayed by HPLC with electrochemical detection. Following systemic administration of salicylate, stable baseline levels of 2,3- and 2,5-DHBA were observed before ischemia. During 20 min of normothermic ischemia, a 50% reduction in mean levels of both DHBAs was documented, suggesting a baseline level of hydroxyl radical that was diminished during ischemia, presumably owing to oxygen restriction to tissue at that time. During recirculation, 2,3- and 2,5-DHBA levels increased by 2.5- and 2.8-fold, respectively. Levels of 2,3-DHBA remained elevated during 1 h of reperfusion, whereas the increase in 2,5-DHBA persisted for 2 h. The increases in 2,3- and 2,5-DHBA levels observed following hyperthermic ischemia were significantly higher (3.8- and fivefold, respectively). In contrast, no significant changes in DHBA levels were observed following hypothermic ischemia.(ABSTRACT TRUNCATED AT 250 WORDS)
为获取不同缺血期温度下脑缺血过程中氧自由基活性的直接证据,我们采用了一种基于水杨酸给药后以稳定加合物2,3 - 二羟基苯甲酸和2,5 - 二羟基苯甲酸(DHBA)形式化学捕获羟自由基的方法。Wistar大鼠通过双血管闭塞加全身低血压(50 mmHg)进行20分钟的全脑缺血。缺血期纹状体温度维持在正常体温(37℃)、低温(30℃)或高温(39℃),但在缺血前后保持在37℃。水杨酸通过全身给药(200 mg/kg,腹腔注射)或通过植入纹状体的微透析探针持续输注(5 mM)。在缺血前、缺血期间和缺血后定期采集纹状体细胞外液样本,并通过高效液相色谱电化学检测法测定2,3 - 和2,5 - DHBA的水平。水杨酸全身给药后,缺血前观察到2,3 - 和2,5 - DHBA的稳定基线水平。在20分钟的正常体温缺血期间,两种DHBA的平均水平均降低了50%,这表明存在一个在缺血期间减少的羟自由基基线水平,可能是由于当时组织的氧供应受限。在再灌注期间,2,3 - 和2,5 - DHBA水平分别增加了2.5倍和2.8倍。在再灌注1小时内,2,3 - DHBA水平持续升高,而2,5 - DHBA的升高持续2小时。高温缺血后观察到的2,3 - 和2,5 - DHBA水平的升高明显更高(分别为3.8倍和5倍)。相比之下,低温缺血后DHBA水平未观察到显著变化。(摘要截短至250字)