Shuaib A, Waqar T, Wishart T, Kanthan R
Saskatchewan Stroke Research Centre, Saskatoon, Canada.
Neurosci Lett. 1995 May 19;191(1-2):87-90. doi: 10.1016/0304-3940(95)11567-0.
Hypothermia or a glutamate receptor antagonist may offer protection when used before or within seconds of an ischemic insult. In this experiment, we tested the efficacy of hypothermia (34 degrees C) versus CGS-19755 (a potent competitive N-methyl-D-aspartate (NMDA) receptor blocker) and their combination which was administered 0.5 h after a 5-min forebrain ischemic insult in gerbils. Morphological assessments were done in Group A at the end of 7 days while Group B was evaluated at 29 days. Each group had four sets of animals: saline treated controls; hypothermia treated; CGS-19755 treated; and a combination of CGS-19755 + hypothermia treated animals. Group A showed significant 'protection', i.e. minimal neuronal damage in the animals treated with hypothermia alone. Protection was evident in the cerebral cortex (P < 0.001), hippocampus CA1 (P < 0.01), and in the striatum (P < 0.05). There was no evidence of neuronal protection in the animals that had received either CGS-19755 alone or a combination of hypothermia and CGS-19755. In Group B (29 day assessment) the neuroprotective effects were not evident in any of the animals when compared to the controls. Behavioral testing with Morris water-maze testing showed no significant differences between the control and any of the treated animals. Our data suggests that 'post-ischemic' therapy with hypothermia may delay the effects of ischemia but does not offer significant long-term neuronal protection. Protection seen at 7 days is not evident at 29 days.(ABSTRACT TRUNCATED AT 250 WORDS)
在缺血性损伤前或损伤后数秒内使用低温疗法或谷氨酸受体拮抗剂可能具有保护作用。在本实验中,我们测试了低温(34摄氏度)与CGS - 19755(一种强效竞争性N - 甲基 - D - 天冬氨酸(NMDA)受体阻滞剂)及其联合用药的效果,这些药物是在沙土鼠经历5分钟前脑缺血损伤后0.5小时给予的。形态学评估在第7天结束时对A组进行,而B组在第29天进行评估。每组有四组动物:生理盐水处理的对照组;低温处理组;CGS - 19755处理组;以及CGS - 19755与低温联合处理组。A组显示出显著的“保护”作用,即单独接受低温处理的动物神经元损伤最小。在大脑皮层(P < 0.001)、海马CA1区(P < 0.01)和纹状体(P < 0.05)中保护作用明显。单独接受CGS - 19755或低温与CGS - 19755联合处理的动物没有神经元保护的证据。在B组(29天评估)中,与对照组相比,任何动物都没有明显的神经保护作用。用莫里斯水迷宫测试进行的行为测试表明,对照组与任何处理组动物之间没有显著差异。我们的数据表明,低温“缺血后”疗法可能会延迟缺血的影响,但不能提供显著的长期神经元保护。在第7天看到的保护作用在第29天并不明显。(摘要截断于250字)