Duszczyk Małgorzata, Ziembowicz Apolonia, Gadamski Roman, Lazarewicz Jerzy W
Department of Neurochemistry, Medical Research Centre, Polish Academy of Sciences, 5 Pawifiskiego St, 02-106 Warsaw, Poland.
Acta Neurobiol Exp (Wars). 2006;66(4):311-9. doi: 10.55782/ane-2006-1620.
In Mongolian gerbils, global forebrain ischemia induces enhanced locomotor activity and the disruption of nest building immediately after the insult, followed by damage to hippocampal neurons developing 3 days later. Preconditioning by a brief episode of sublethal ischemia induces the protection of CA1 hippocampal neurons against a lethal ischemic insult. We examined how preconditioning with 2-min ischemia affects disturbances in the nest building behavior and locomotor activity induced by the injurious 3-min ischemia. Morphological examination confirmed that preconditioning significantly reduced neuronal damage in CA1 evoked by injurious ischemia. Behavioral studies demonstrated that preconditioning reduced the locomotor hyperactivity and latency in nest building after test ischemia, in comparison to sham or naive animals. The results indicate that the nest building test and measurement of locomotor activity may be used for an early in vivo prediction of the extent of ischemic brain damage and tolerance induced by ischemic preconditioning.
在蒙古沙鼠中,全脑缺血在损伤后立即会导致运动活动增强和筑巢行为紊乱,随后在3天后会出现海马神经元损伤。短暂的亚致死性缺血预处理可诱导对CA1海马神经元的保护,使其免受致死性缺血损伤。我们研究了2分钟缺血预处理如何影响由3分钟损伤性缺血诱导的筑巢行为和运动活动紊乱。形态学检查证实,预处理显著减少了损伤性缺血诱发的CA1区神经元损伤。行为学研究表明,与假手术或未处理动物相比,预处理降低了测试性缺血后运动活动亢进和筑巢延迟。结果表明,筑巢试验和运动活动测量可用于早期体内预测缺血性脑损伤的程度以及缺血预处理诱导的耐受性。