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首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >Five percent, 7.5% or 10% hypertonic saline prevents delayed neuronal death in gerbils: (Une solution saline a 5 %, 7,5 % ou 10 % empeche la mort neuronale differee chez des gerbilles).
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Five percent, 7.5% or 10% hypertonic saline prevents delayed neuronal death in gerbils: (Une solution saline a 5 %, 7,5 % ou 10 % empeche la mort neuronale differee chez des gerbilles).

机译:5%,7.5%或10%的高渗盐水可防止沙鼠的神经元延迟死亡:( 5%,7.5%或10%的盐溶液可防止沙鼠的神经元延迟死亡)。

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PURPOSE: To clarify the appropriate concentration and dose of hypertonic saline solution (HSS) for preventing delayed neuronal death in the hippocampal CA1 subfield after transient forebrain ischemia in gerbils. METHODS: Thirty gerbils were randomly assigned to five groups: physiological saline solution (PSS) group, ischemia/reperfusion treated with PSS 2 mL*kg(-1); 5% HSS group, treated with 5% HSS 2 mL*kg(-1); 7.5% HSS group, treated with 7.5% HSS 2 mL*kg(-1); 10% HSS group, treated with 10% HSS 2 mL*kg(-1); 20% HSS group, treated with 20% HSS 2 mL*kg(-1). Transient forebrain ischemia was induced by occluding the bilateral common carotid arteries for four minutes. Five days later, histopathological changes in the hippocampal area were examined, and the degenerative ratio of the pyramidal cells were measured according to the following formula: (number of degenerative pyramidal cells/total number of pyramidal cells per 1 mm of hippocampal CA1 subfield) x 100. RESULTS: In PSS and 20% groups, neuronal cell damage was observed five days after ischemia. In the other three groups, these changes were not observed. The degenerative ratios of pyramidal cells were as follows; PSS group: 91.6 +/- 5.6%, 5% HSS group: 7.2 +/- 1.6%, 7.5% group: 8.3 +/- 1.4%, 10% HSS group: 6.2 +/- 1.1%, 20% HSS group: 85.8 +/- 8.7% (P < 0.05; PSS and 20% HSS vs three other groups). CONCLUSION: This study demonstrates that 5, 7.5 or 10% HSS 2 mL*kg(-1) may prevent delayed neuronal death in the hippocampal CA1 subfield after cerebral ischemia/reperfusion in gerbils.
机译:目的:阐明高渗盐溶液(HSS)的适当浓度和剂量,以防止沙土鼠短暂性前脑缺血后海马CA1子区延迟神经元死亡。方法:将30只沙鼠随机分为5组:生理盐溶液(PSS)组,2 mL * kg(-1)PSS处理缺血/再灌注; 5%HSS组,5%HSS 2 mL * kg(-1)处理; 7.5%HSS组,以7.5%HSS 2 mL * kg(-1)处理; 10%HSS组,10%HSS 2 mL * kg(-1)处理; 20%HSS组,用20%HSS 2 mL * kg(-1)处理。通过阻塞双侧颈总动脉四分钟来诱发短暂性前脑缺血。五天后,检查海马区的组织病理学变化,并根据以下公式测量锥体细胞的退化率:(退化的锥体细胞数量/每1 mm海马CA1子域锥体细胞总数)x 100.结果:在PSS和20%的组中,缺血5天后观察到神经元细胞损伤。在其他三组中,未观察到这些变化。锥体细胞的退化率如下: PSS组:91.6 +/- 5.6%,5%HSS组:7.2 +/- 1.6%,7.5%组:8.3 +/- 1.4%,10%HSS组:6.2 +/- 1.1%,20%HSS组: 85.8 +/- 8.7%(P <0.05; PSS和20%HSS与其他三个组相比)。结论:这项研究表明5、7.5或10%HSS 2 mL * kg(-1)可以防止沙鼠脑缺血/再灌注后海马CA1子区的神经元延迟死亡。

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