Suppr超能文献

低温对凝血酶诱导的脑水肿形成的影响。

Effects of hypothermia on thrombin-induced brain edema formation.

作者信息

Kawai N, Kawanishi M, Okauchi M, Nagao S

机构信息

Department of Neurological Surgery, Kagawa Medical University, 1750-1 Ikenobe, Miki-cho, Kita-gun, Kagawa 761-0793, Japan.

出版信息

Brain Res. 2001 Mar 23;895(1-2):50-8. doi: 10.1016/s0006-8993(01)02026-1.

Abstract

Recent studies have shown that thrombin plays an important role in brain edema formation after intracerebral hemorrhage (ICH). The possible mechanisms of thrombin-induced brain edema formation include blood-brain barrier (BBB) disruption and inflammatory response involving polymorphonuclear (PMN) leukocyte. Animal experiments have revealed that moderate therapeutic hypothermia improves pathological and functional outcome in various models of brain injury. In this study, we examined the effect of hypothermia on thrombin-induced brain edema formation. Effects of hypothermia on BBB permeability and the accumulation of PMN leukocytes were also determined to clarify the protective mechanism of hypothermia in this model. Anesthetized adult rats received an injection of 10 Units of thrombin into the basal ganglia. Animals were separated into the normothermic and hypothermic groups, which were housed in a room maintained at 25 degrees C and in a cold room maintained at 5 degrees C, respectively, for 24 h after the thrombin injection. The brain temperature in rats housed in a cold room reduced temporarily to approximately 30 degrees C and then gradually recovered to 35 degrees C by the end of the observation. Brain water content in the basal ganglia was significantly reduced in rats treated with hypothermia compared to the normothermic rats (84.3+/-0.2 vs. 82.4+/-0.1%; P<0.01). The decrease of brain water content was accompanied with a significant reduction in BBB permeability to Evan's blue dye and in accumulation of PMN leukocytes. This study indicates that hypothermic treatment significantly reduces thrombin-induced brain edema formation in the rat. Inhibition of thrombin-induced BBB breakdown and inflammatory response by hypothermia appear to contribute to brain protection in this model. Hypothermic treatment may provide an approach to potentially reduce ongoing edema after ICH.

摘要

近期研究表明,凝血酶在脑出血(ICH)后脑水肿形成过程中起重要作用。凝血酶诱导脑水肿形成的可能机制包括血脑屏障(BBB)破坏以及涉及多形核(PMN)白细胞的炎症反应。动物实验显示,适度治疗性低温可改善各种脑损伤模型的病理和功能结局。在本研究中,我们检测了低温对凝血酶诱导的脑水肿形成的影响。还测定了低温对血脑屏障通透性和PMN白细胞积聚的影响,以阐明该模型中低温的保护机制。将成年麻醉大鼠基底神经节注射10单位凝血酶。动物被分为常温组和低温组,分别在凝血酶注射后于25℃的房间和5℃的冷房间饲养24小时。饲养在冷房间的大鼠脑温暂时降至约30℃,然后在观察结束时逐渐恢复至35℃。与常温大鼠相比,低温治疗的大鼠基底神经节脑含水量显著降低(84.3±0.2 vs. 82.4±0.1%;P<0.01)。脑含水量的降低伴随着血脑屏障对伊文思蓝染料的通透性以及PMN白细胞积聚的显著减少。本研究表明,低温治疗可显著减轻大鼠凝血酶诱导的脑水肿形成。低温对凝血酶诱导的血脑屏障破坏和炎症反应的抑制作用似乎有助于该模型中的脑保护。低温治疗可能为潜在减轻脑出血后持续的水肿提供一种方法。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验