首页> 外文期刊>Journal of neurotrauma >Influence of posttraumatic hypoxia on behavioral recovery and histopathological outcome following moderate spinal cord injury in rats.
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Influence of posttraumatic hypoxia on behavioral recovery and histopathological outcome following moderate spinal cord injury in rats.

机译:创伤后低氧对大鼠中度脊髓损伤后行为恢复和组织病理学结果的影响。

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Pulmonary dysfunction leading to secondary hypoxia is a common complication of spinal cord injury (SCI). The purpose of this study was to clarify the behavioral and histopathological consequences of posttraumatic hypoxia in an established model of traumatic SCI. Forty-five female Sprague-Dawley rats were randomly assigned to one of four groups, including (1) laminectomy and normoxia (n = 10), (2) laminectomy and hypoxia (n = 11), (3) NYU weight-drop and normoxia (n = 12), and (4) NYU weight-drop and hypoxia (n = 11). For these studies, a moderate injury was induced by adjusting the height of the weight drop (10 g) to 12.5 mm above the exposed spinal cord (T10). Immediately after injury, PaO2 in the hypoxic rats was kept between 30 and 35 mm Hg for 30 min. PaO2 in the normoxic group was maintained over 100 mm Hg, while PaCO2 in all rats was maintained at 35-40 mm Hg. The behavior of the rats was checked every 7 days using the Basso, Beattie, and Bresnahan (BBB) locomotor rating scale. Rats were sacrificed at 8 weeks for quantitative histopathological analysis of lesion areas. During the hypoxic insults, the mean arterial blood pressure dropped in both sham control and weight-drop rats (p < 0.01). At the end of the 8-week monitoring period, BBB scores were 12.5 +/- 3.1 (mean +/- SEM) and 14.2 +/- 3.4 in the normoxic and hypoxic traumatized rats, respectively. No significant difference between the traumatized groups was documented with BBB monitoring. In contrast, the percent of gray matter necrosis at the impact epicenter was significantly increased in hypoxic versus normoxic SCI rats (p < 0.01). These data demonstrate that posttraumatic hypoxia complicated by mild hypotension aggravates the histopathological consequences of SCI and further emphasize the need to control for secondary hypoxic insults after experimental and clinical SCI. Potential explanations for the lack of a correlation between the behavioral and histopathological findings are discussed.
机译:导致继发性缺氧的肺功能障碍是脊髓损伤(SCI)的常见并发症。这项研究的目的是在创伤性SCI建立的模型中阐明创伤后低氧的行为和组织病理学后果。将45只雌性Sprague-Dawley大鼠随机分为四组之一,包括(1)椎板切除术和常氧(n = 10),(2)椎板切除术和缺氧(n = 11),(3)NYU体重减轻和常氧(n = 12),以及(4)NYU体重减轻和缺氧(n = 11)。对于这些研究,通过将重量下降(10 g)的高度调整到暴露的脊髓(T10)上方12.5 mm,可引起中度伤害。受伤后立即将缺氧大鼠的PaO2保持在30至35 mm Hg之间30分钟。常氧组的PaO2维持在100 mm Hg以上,而所有大鼠的PaCO2维持在35-40 mm Hg。每隔7天使用Basso,Beattie和Bresnahan(BBB)运动评分量表检查一次大鼠的行为。在第8周处死大鼠以对病变区域进行定量组织病理学分析。在低氧损伤期间,假手术对照组和体重减轻大鼠的平均动脉血压均下降(p <0.01)。在为期8周的监测期结束时,常氧和低氧创伤后大鼠的BBB评分分别为12.5 +/- 3.1(平均+/- SEM)和14.2 +/- 3.4。 BBB监测显示,受创组之间无显着差异。相反,低氧和常氧的SCI大鼠在撞击震中的灰质坏死百分比显着增加(p <0.01)。这些数据表明,创伤后低氧并发轻度低血压会加重SCI的组织病理学后果,并进一步强调需要在实验和临床SCI后控制继发性低氧损伤。讨论了行为和组织病理学发现之间缺乏相关性的潜在解释。

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