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米诺环素可减少脑积水大鼠模型中的反应性神经胶质增生。

Minocycline reduces reactive gliosis in the rat model of hydrocephalus.

机构信息

Department of Neurosurgery, First Affiliate Hospital of Xiamen University, Xiamen, Fujian Province 361003, China.

出版信息

BMC Neurosci. 2012 Dec 5;13:148. doi: 10.1186/1471-2202-13-148.

DOI:10.1186/1471-2202-13-148
PMID:23217034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3529686/
Abstract

BACKGROUND

Reactive gliosis had been implicated in injury and recovery patterns associated with hydrocephalus. Our aim is to determine the efficacy of minocycline, an antibiotic known for its anti-inflammatory properties, to reduce reactive gliosis and inhibit the development of hydrocephalus.

RESULTS

The ventricular dilatation were evaluated by MRI at 1-week post drugs treated, while GFAP and Iba-1were detected by RT-PCR, Immunohistochemistry and Western blot. The expression of GFAP and Iba-1 was significantly higher in hydrocephalic group compared with saline control group (p < 0.05). Minocycline treatment of hydrocephalic animals reduced the expression of GFAP and Iba-1 significantly (p < 0.05). Likewise, the severity of ventricular dilatation is lower in minocycline treated hydrocephalic animals compared with the no minocycline group (p < 0.05).

CONCLUSION

Minocycline treatment is effective in reducing the gliosis and delaying the development of hydrocephalus with prospective to be the auxiliary therapeutic method of hydrocephalus.

摘要

背景

反应性神经胶质增生与脑积水相关的损伤和恢复模式有关。我们的目的是确定米诺环素(一种以其抗炎特性而闻名的抗生素)的功效,以减少反应性神经胶质增生并抑制脑积水的发展。

结果

在药物治疗后 1 周通过 MRI 评估脑室扩张,同时通过 RT-PCR、免疫组织化学和 Western blot 检测 GFAP 和 Iba-1。与盐水对照组相比,脑积水组的 GFAP 和 Iba-1 表达显著升高(p<0.05)。米诺环素治疗脑积水动物可显著降低 GFAP 和 Iba-1 的表达(p<0.05)。同样,米诺环素治疗的脑积水动物的脑室扩张严重程度低于无米诺环素组(p<0.05)。

结论

米诺环素治疗可有效减少神经胶质增生并延缓脑积水的发展,有望成为脑积水的辅助治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52e/3529686/f50a8de092f1/1471-2202-13-148-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52e/3529686/fd666df3ec0b/1471-2202-13-148-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52e/3529686/fccc8f241062/1471-2202-13-148-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52e/3529686/7b247a9732a2/1471-2202-13-148-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52e/3529686/cd44829395fa/1471-2202-13-148-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52e/3529686/f50a8de092f1/1471-2202-13-148-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52e/3529686/fd666df3ec0b/1471-2202-13-148-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52e/3529686/fccc8f241062/1471-2202-13-148-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52e/3529686/7b247a9732a2/1471-2202-13-148-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52e/3529686/cd44829395fa/1471-2202-13-148-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52e/3529686/f50a8de092f1/1471-2202-13-148-5.jpg

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Childs Nerv Syst. 2011 Oct;27(10):1535-41. doi: 10.1007/s00381-011-1558-y. Epub 2011 Sep 17.
3
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Exp Neurol. 2023 Nov;369:114523. doi: 10.1016/j.expneurol.2023.114523. Epub 2023 Aug 30.
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After Ischemic Stroke, Minocycline Promotes a Protective Response in Neurons via the RNA-Binding Protein HuR, with a Positive Impact on Motor Performance.缺血性脑卒中后,米诺环素通过 RNA 结合蛋白 HuR 促进神经元的保护反应,对运动功能产生积极影响。
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