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白细胞介素-18对小鼠短暂性局灶性脑缺血早期的梗死体积或功能结局无影响。

Interleukin-18 does not influence infarct volume or functional outcome in the early stage after transient focal brain ischemia in mice.

作者信息

Braeuninger Stefan, Kleinschnitz Christoph, Stoll Guido

机构信息

Department of Neurology, Julius-Maximilians-Universitaet Wuerzburg, Josef-Schneider-Strasse 11, D-97080 Wuerzburg, Germany.

出版信息

Exp Transl Stroke Med. 2010 Jan 5;2:1. doi: 10.1186/2040-7378-2-1.

Abstract

Interleukin-18 (IL-18) is a proinflammatory cytokine of the interleukin-1 family which is upregulated after cerebral ischemia. The functional role of IL-18 in cerebral ischemia is unknown. In the present study, we compared infarct size in IL-18 knock-out and wild-type mice 24 hours and 48 hours after 1-hour transient middle cerebral artery occlusion (tMCAO). Moreover, the functional outcome was evaluated in a modified Bederson score, foot fault test and grip test. There were no significant differences in infarct size or functional outcome tests between wild-type and IL-18 knock-out mice. These data indicate that the early inflammatory response to cerebral ischemia does not involve IL-18, in contrast to other interleukin-1 family members such as interleukin-1.

摘要

白细胞介素-18(IL-18)是白细胞介素-1家族的一种促炎细胞因子,在脑缺血后上调。IL-18在脑缺血中的功能作用尚不清楚。在本研究中,我们比较了IL-18基因敲除小鼠和野生型小鼠在1小时短暂性大脑中动脉闭塞(tMCAO)后24小时和48小时的梗死面积。此外,通过改良的贝德森评分、足误试验和握力试验评估功能结局。野生型小鼠和IL-18基因敲除小鼠在梗死面积或功能结局测试方面没有显著差异。这些数据表明,与白细胞介素-1等其他白细胞介素-1家族成员不同,脑缺血的早期炎症反应不涉及IL-18。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f9b/2820471/59d6ea32b515/2040-7378-2-1-1.jpg

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