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高压氧疗法减轻颅脑损伤继发性脑损伤:脑挫伤动物模型

Hyperbaric oxygen therapy for reduction of secondary brain damage in head injury: an animal model of brain contusion.

作者信息

Palzur Eilam, Vlodavsky Eugene, Mulla Hani, Arieli Ran, Feinsod Moshe, Soustiel Jean F

机构信息

Division of Neurosurgery and Acute Brain Research Laboratory, Rambam Medical Center, Faculty of Medicine, The Technion, Haifa, Israel.

出版信息

J Neurotrauma. 2004 Jan;21(1):41-8. doi: 10.1089/089771504772695931.

Abstract

Cerebral contusions are one the most frequent traumatic lesions and the most common indication for secondary surgical decompression. The purpose of this study was to investigate the physiology of perilesional secondary brain damage and evaluate the value of hyperbaric oxygen therapy (HBOT) in the treatment of these lesions. Five groups of five Sprague-Dawley rats each were submitted to dynamic cortical deformation (DCD) induced by negative pressure applied to the cortex. Cerebral lesions produced by DCD at the vacuum site proved to be reproducible. The study protocol entailed the following: (1) DCD alone, (2) DCD and HBOT, (3) DCD and post-operative hypoxia and HBOT, (4) DCD, post-operative hypoxia and HBOT, and (5) DCD and normobaric hyperoxia. Animals were sacrificed after 4 days. Histological sections showed localized gross tissue loss in the cortex at injury site, along with hemorrhage. In all cases, the severity of secondary brain damage was assessed by counting the number of terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) and caspase 3-positive cells in successive perilesional layers, each 0.5 mm thick. Perilesional TUNEL positive cells suggested the involvement of apoptosis in group 1 (12.24% of positive cells in layer 1). These findings were significantly enhanced by post-operative hypoxia (31.75%, p < 0.001). HBOT significantly reduced the severity and extent of secondary brain damage expressed by the number of TUNEL positive cells in each layer and the volume of the lesion (4.7% and 9% of TUNEL positive cells in layer 1 in groups 2 and 4 respectively, p < 0.0001 and p < 0.003). Normobaric hyperoxia also proved to be beneficial although in a lesser extent. This study demonstrates that the vacuum model of brain injury is a reproducible model of cerebral contusion. The current findings also suggest that HBOT may limit the growth of cerebral contusions and justify further experimental studies.

摘要

脑挫伤是最常见的创伤性损伤之一,也是二次手术减压最常见的适应症。本研究的目的是探讨损伤灶周围继发性脑损伤的生理机制,并评估高压氧治疗(HBOT)对这些损伤的治疗价值。将五组,每组五只Sprague-Dawley大鼠置于负压作用于皮质所诱导的动态皮质变形(DCD)模型中。在真空部位由DCD产生的脑损伤被证明是可重复的。研究方案如下:(1)仅DCD;(2)DCD和HBOT;(3)DCD及术后缺氧和HBOT;(4)DCD、术后缺氧和HBOT;(5)DCD和常压高氧。4天后处死动物。组织学切片显示损伤部位皮质有局部明显的组织损失,伴有出血。在所有病例中,通过计数连续的损伤灶周围层(每层厚0.5mm)中末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)和半胱天冬酶3阳性细胞的数量来评估继发性脑损伤的严重程度。损伤灶周围TUNEL阳性细胞提示第1组(第1层阳性细胞占12.24%)存在凋亡。术后缺氧显著增强了这些发现(31.75%,p<0.001)。HBOT显著降低了每层TUNEL阳性细胞数量和损伤体积所表示的继发性脑损伤的严重程度和范围(第2组和第4组第1层TUNEL阳性细胞分别占4.7%和9%,p<0.0001和p<0.003)。常压高氧也被证明是有益的,尽管程度较小。本研究表明,脑损伤的真空模型是一种可重复的脑挫伤模型。目前的研究结果还表明,HBOT可能会限制脑挫伤的发展,并为进一步的实验研究提供依据。

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