两种实验性脑出血模型体液性神经炎症及黏附分子表达的比较。

Arthur Liesz, Moritz Middelhoff, Wei Zhou, Simone Karcher, Sergio Illanes, Roland Veltkamp
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引用次数: 39

摘要

背景:炎症级联反应通过体液因子和细胞介导的细胞毒性参与脑出血(ICH)后的继发性损伤。先前开发了几个实验模型来分析出血性神经炎症。然而,到目前为止,神经炎症标志物还没有在这些模型之间进行面对面的比较,因此,仅从一个个体模型得出的病理生理学结论可能并不有效。方法:我们比较了两种最常见的小鼠模型:纹状体注射自体血和胶原酶的神经炎症途径。RT-PCR分析ICH诱导后多个时间点促炎因子、抗炎因子(IL-1、TNF-α、IFN-γ、IL-6、TGF-β、IL-10)表达及粘附分子(VCAM-1、ICAM-1)表达。比较两种模型的预后和生理参数。结果:两种模型均诱导促炎细胞因子和粘附分子的表达显著和动态增加。然而,血液注射导致这些标记物的改变比胶原酶注射明显更明显。尽管脑出血体积相等,但与胶原酶模型相比,这种差异与输血后的预后较差有关。结论:这是首次对两种最广泛使用的小鼠脑出血模型的神经炎症途径进行面对面比较的研究,揭示了模型之间的实质性差异。在设计采用实验性脑出血模型的未来研究时,特别是在分析神经炎症途径和治疗方法时,需要考虑到这种差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Comparison of humoral neuroinflammation and adhesion molecule expression in two models of experimental intracerebral hemorrhage.

Background: Inflammatory cascades contribute to secondary injury after intracerebral hemorrhage (ICH) via humoral factors and cell-mediated cytotoxicity. Several experimental models were previously developed to analyze post-hemorrhagic neuroinflammation. However, neuroinflammatory markers have not been compared face-to-face between these models so far, and therefore, pathophysiological conclusions drawn from only one individual model may not be valid.

Methods: We compared neuroinflammatory pathways in the two most common murine models: striatal injection of autologous blood or collagenase. Expression of pro- and anti-inflammatory cytokines (IL-1, TNF-α, IFN-γ, IL-6, TGF-β and IL-10) as well adhesion molecule expression (VCAM-1, ICAM-1) was analyzed by RT-PCR at several time points after ICH induction. Outcome and physiological parameters were compared between the models.

Results: Both models induced a profound and dynamic increase in the expression of pro-inflammatory cytokines and adhesion molecules. However, blood injection resulted in significantly more pronounced alteration of these markers than collagenase injection. This difference was associated with worse outcome after blood injection compared to the collagenase model despite equal ICH volumes.

Conclusions: This is the first study performing a face-to-face comparison of neuroinflammatory pathways in the two most widely used murine ICH models, revealing substantial differences between the models. This discrepancies need to be taken into account in designing future studies employing experimental ICH models, especially when analyzing neuroinflammatory pathways and therapies.

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