Suppr超能文献

白三烯抑制剂对实验性脑挫裂伤演变的影响。

Effect of leukotriene inhibitors on evolution of experimental brain contusions.

机构信息

Department of Neurosurgery, University Hospital of Leipzig, Germany.

出版信息

Neuropathol Appl Neurobiol. 2012 Jun;38(4):354-66. doi: 10.1111/j.1365-2990.2011.01211.x.

Abstract

AIMS

Leukotriene levels increase in cerebrospinal fluid (CSF) following controlled cortical impact (CCI) injury in rats. We investigated the impact of two different leukotriene inhibitors in the CCI model on CSF leukotriene levels, brain water content (BWC), brain swelling (BS) contusion size and cellular response.

METHODS

134 male Sprague Dawley rats were investigated at 4, 24 and 72 h after CCI for CSF leukotriene levels and BWC/BS, lesion size in T2-weighted magnetic resonance imaging and immunohistochemistry. Animals received vehicle, MK-886, an inhibitor of 5-lipoxygenase activating protein, or Boscari(®) , a mixture of boswellic acids, acting as competitive nonredox 5-lipoxygenase inhibitors before trauma and then every 8 h until sacrifice.

RESULTS

The intracranial pressure (ICP) was unaffected by treatment. Boscari treatment reduced CSF leukotriene C4 increase by -45% at 4 h (P < 0.03) and increase of BWC and BS by 49% (P < 0.05) and -58% at 24 h. Treatment with both substances showed a reduction of lesion volume at 72 h by -21% (P < 0.01) in T(2) -weighted magnetic resonance imaging, which was reflected in a smaller lesion area determined from a NeuN labelled section (-17% to -20%, P < 0.05). Triple immunofluorescence and Fluoro-Jade B staining showed rarefaction of neurones, glia and vasculature in the contusion core, whereas in the pericontusional zone astro- and microglia were upregulated in the presence of dying neurones. Treatment resulted in an improved survival of NeuN labelled neurones in the pericontusional cortex (+15% to +20%, P < 0.05).

CONCLUSIONS

Leukotriene inhibition should be further investigated as therapeutic option to counteract secondary growth of traumatic brain contusions and to possibly improve pericontusional neuronal survival.

摘要

目的

在大鼠的皮质控制损伤(CCI)后,白三烯水平在脑脊液(CSF)中增加。我们研究了两种不同的白三烯抑制剂在 CCI 模型中对 CSF 白三烯水平、脑水含量(BWC)、脑肿胀(BS)挫伤大小和细胞反应的影响。

方法

在 CCI 后 4、24 和 72 小时,134 只雄性 Sprague Dawley 大鼠进行了 CSF 白三烯水平和 BWC/BS、T2 加权磁共振成像和免疫组织化学检测。动物在创伤前和之后每 8 小时接受载体、MK-886(5-脂氧合酶激活蛋白抑制剂)或 Boscari(®)(作为竞争性非氧化 5-脂氧合酶抑制剂的混合 Boswellic 酸)治疗,直到处死。

结果

颅内压(ICP)不受治疗影响。Boscari 治疗可使 CSF 白三烯 C4 在 4 小时时降低 45%(P < 0.03),BWC 和 BS 在 24 小时时降低 49%(P < 0.05)和 58%。两种物质的联合治疗可使 T2 加权磁共振成像中的病变体积在 72 小时时减少 21%(P < 0.01),这反映在从 NeuN 标记切片中确定的病变面积减少了 17%至 20%(P < 0.05)。三重免疫荧光和 Fluoro-Jade B 染色显示挫伤核心的神经元、胶质细胞和血管稀疏,而在周围挫伤区,星形胶质细胞和小胶质细胞在死亡神经元存在时上调。治疗导致在周围皮质中 NeuN 标记的神经元存活增加 15%至 20%(P < 0.05)。

结论

白三烯抑制作用应作为治疗选择进一步研究,以对抗创伤性脑挫伤的继发性生长,并可能改善周围神经元的存活。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验