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癫痫持续状态后大鼠海马中表达白细胞介素-1β的细胞的动态变化

Dynamic Change in Cells Expressing IL-1β in Rat Hippocampus after Status Epilepticus.

作者信息

Sakuma Satoru, Tokuhara Daisuke, Otsubo Hiroshi, Yamano Tsunekazu, Shintaku Haruo

机构信息

Department of Pediatrics, Osaka City University Graduate School of Medicine, Osaka, Japan.

Division of Neurology, The Hospital for Sick Children, Toronto, Canada.

出版信息

Jpn Clin Med. 2014 Aug 13;5:25-32. doi: 10.4137/JCM.S13738. eCollection 2014.

Abstract

BACKGROUND

The time course of cytokine dynamics after seizure remains controversial. Here we evaluated the changes in the levels and sites of interleukin (IL)-1β expression over time in the hippocampus after seizure.

METHODS

Status epilepticus (SE) was induced in adult Wistar rats by means of intraperitoneal injection of kainic acid (KA). Subsequently, the time courses of cellular localization and IL-1β concentration in the hippocampus were evaluated by means of immunohistochemical and quantitative assays.

RESULTS

On day 1 after SE, CA3 pyramidal cells showed degeneration and increased IL-1β expression. In the chronic phase (>7 days after SE), glial fibrillary acidic protein (GFAP)-positive reactive astrocytes-appeared in CA1 and became IL-1β immunoreactive. Their IL-1β immunoreactivity increased in proportion to the progressive hypertrophy of astrocytes that led to gliosis. Quantitative analysis showed that hippocampal IL-1β concentration progressively increased during the acute and chronic phases.

CONCLUSION

IL-1β affects the hippocampus after SE. In the acute phase, the main cells expressing IL-1β were CA3 pyramidal cells. In the chronic phase, the main cells expressing IL-1β were reactive astrocytes in CA1.

摘要

背景

癫痫发作后细胞因子动力学的时间进程仍存在争议。在此,我们评估了癫痫发作后海马体中白细胞介素(IL)-1β表达水平和位点随时间的变化。

方法

通过腹腔注射海藻酸(KA)在成年Wistar大鼠中诱导癫痫持续状态(SE)。随后,通过免疫组织化学和定量分析评估海马体中细胞定位和IL-1β浓度的时间进程。

结果

在SE后的第1天,CA3锥体细胞出现退化且IL-1β表达增加。在慢性期(SE后>7天),胶质纤维酸性蛋白(GFAP)阳性的反应性星形胶质细胞出现在CA1区并变得具有IL-1β免疫反应性。它们的IL-1β免疫反应性随着导致胶质增生的星形胶质细胞逐渐肥大而增加。定量分析表明,海马体IL-1β浓度在急性期和慢性期逐渐升高。

结论

IL-1β在SE后影响海马体。在急性期,表达IL-1β的主要细胞是CA3锥体细胞。在慢性期,表达IL-1β的主要细胞是CA1区的反应性星形胶质细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8198/4134005/c3d1c93754a5/jcm-5-2014-025f1.jpg

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