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

机译:两种实验性脑出血模型中体液神经炎症和粘附分子表达的比较

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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.
机译:背景炎症级联反应通过体液因子和细胞介导的细胞毒性作用,导致脑出血(ICH)后继发性损伤。先前已经开发了几种实验模型来分析出血后神经炎症。但是,到目前为止,尚未在这些模型之间进行面对面的神经炎症标记物比较,因此,仅从一个模型得出的病理生理学结论可能无效。方法我们比较了两种最常见的鼠模型的神经炎途径:纹状体注射自体血或胶原酶。分析促炎和抗炎细胞因子(IL-1,TNF-α,IFN-γ,IL-6,TGF-β和IL-10)的表达以及粘附分子的表达(VCAM-1,ICAM-1)在ICH诱导后几个时间通过RT-PCR进行检测。在模型之间比较结果和生理参数。结果两种模型均引起促炎性细胞因子和粘附分子表达的深刻而动态的增加。然而,与胶原酶注射相比,血液注射导致这些标志物的变化明显得多。尽管ICH量相等,但与胶原酶模型相比,这种差异与血液注射后的不良结局有关。结论这是第一项在两个使用最广泛的鼠类ICH模型中进行神经炎症途径面对面比较的研究,揭示了模型之间的实质性差异。在设计使用实验性ICH模型的未来研究时,尤其是在分析神经炎性途径和疗法时,需要考虑这种差异。

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