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本文引用的文献

1
Vascular recovery promoted by atorvastatin and simvastatin after experimental intracerebral hemorrhage: magnetic resonance imaging and histological study.阿托伐他汀和辛伐他汀促进实验性脑出血后血管恢复的磁共振成像和组织学研究。
J Neurosurg. 2011 Apr;114(4):1135-42. doi: 10.3171/2010.7.JNS10163. Epub 2010 Aug 20.
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Statins in traumatic brain injury.他汀类药物在创伤性脑损伤中的应用。
Neurotherapeutics. 2010 Jan;7(1):62-73. doi: 10.1016/j.nurt.2009.11.003.
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Dynamics and functions of tight junctions.紧密连接的动态与功能。
Trends Cell Biol. 2010 Mar;20(3):142-9. doi: 10.1016/j.tcb.2009.12.002. Epub 2010 Jan 12.
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Simvastatin and atorvastatin improve neurological outcome after experimental intracerebral hemorrhage.辛伐他汀和阿托伐他汀可改善实验性脑出血后的神经功能结局。
Stroke. 2009 Oct;40(10):3384-9. doi: 10.1161/STROKEAHA.108.544395. Epub 2009 Jul 30.
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Prior use of statins and outcome in patients with intracerebral haemorrhage.他汀类药物的先前使用与脑出血患者的结局。
Eur J Neurol. 2010 Jan;17(1):78-83. doi: 10.1111/j.1468-1331.2009.02747.x. Epub 2009 Jul 9.
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Localization of bone marrow stromal cells to the injury site after intracerebral hemorrhage in rats.大鼠脑出血后骨髓基质细胞向损伤部位的定位。
J Neurosurg. 2010 Feb;112(2):329-35. doi: 10.3171/2009.2.JNS08907.
7
Use of statins for the treatment of spontaneous intracerebral hemorrhage: results of a pilot study.他汀类药物用于治疗自发性脑出血:一项初步研究的结果。
Cent Eur Neurosurg. 2009 Feb;70(1):15-20. doi: 10.1055/s-0028-1082064. Epub 2009 Feb 5.
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Blood-brain barrier function in intracerebral hemorrhage.脑出血中的血脑屏障功能。
Acta Neurochir Suppl. 2008;105:73-7. doi: 10.1007/978-3-211-09469-3_15.
9
Temporal MRI assessment of intracerebral hemorrhage in rats.大鼠脑出血的颞部磁共振成像评估
Stroke. 2008 Sep;39(9):2596-602. doi: 10.1161/STROKEAHA.107.506683. Epub 2008 Jul 17.
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Effect of statins on intracerebral hemorrhage outcome and recurrence.他汀类药物对脑出血结局及复发的影响。
Stroke. 2008 Jul;39(7):2151-4. doi: 10.1161/STROKEAHA.107.508861. Epub 2008 Apr 24.

他汀类药物在实验性脑出血后可急性保护血脑屏障。

Statins Protect the Blood Brain Barrier Acutely after Experimental Intracerebral Hemorrhage.

作者信息

Yang Dongmei, Knight Robert A, Han Yuxia, Karki Kishor, Zhang Jianfeng, Chopp Michael, Seyfried Donald M

机构信息

Department of Neurosurgery, Henry Ford Health System, 2799 W Grand Blvd, Detroit, MI 48202.

出版信息

J Behav Brain Sci. 2013 Feb;3(1):100-106. doi: 10.4236/jbbs.2013.31010. Epub 2012 Dec 10.

DOI:10.4236/jbbs.2013.31010
PMID:23459792
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3583226/
Abstract

OBJECTIVES

The goal of this study was to measure the impact of simvastatin and atorvastatin treatment on blood brain barrier (BBB) integrity after experimental intracerebral hemorrhage (ICH).

METHODS

Primary ICH was induced in 27 male Wistar rats by stereotactic injection of 100 µL of autologous blood into the striatum. Rats were divided into three groups (n= 9/group): 1) oral treatment (2 mg/kg) of atorvastatin, 2) oral treatment (2 mg/kg) simvastatin, or 3) phosphate buffered saline daily starting 24-hours post-ICH and continuing daily for the next 3 days. On the fourth day, the animals underwent magnetic resonance imaging (MRI) for measurements of T (a marker for BBB integrity), T (edema), and cerebral blood flow (CBF). After MRI, the animals were sacrificed and immunohistology or Western blotting was performed.

RESULTS

MRI data for animals receiving simvastatin treatment showed significantly reduced BBB dysfunction and improved CBF in the ICH rim compared to controls (<0.05) 4 days after ICH. Simvastatin also significantly reduced edema (T) in the rim at 4 days after ICH (<0.05). Both statin-treated groups demonstrated increased occludin and endothelial barrier antigen levels within the vessel walls, indicating better preservation of BBB function (<0.05) and increased number of blood vessels (<0.05).

CONCLUSIONS

Simvastatin treatment administered acutely after ICH protects BBB integrity as measured by MRI and correlative immunohistochemistry. There was also evidence of improved CBF and reduced edema by MRI. Conversely, atorvastatin showed a non-significant trend by MRI measurement.

摘要

目的

本研究的目的是测量辛伐他汀和阿托伐他汀治疗对实验性脑出血(ICH)后血脑屏障(BBB)完整性的影响。

方法

通过立体定向向27只雄性Wistar大鼠纹状体内注射100μL自体血诱导原发性ICH。大鼠分为三组(每组n = 9):1)阿托伐他汀口服治疗(2mg/kg),2)辛伐他汀口服治疗(2mg/kg),或3)从ICH后24小时开始每日给予磷酸盐缓冲盐水,并在接下来的3天持续每日给药。在第4天,对动物进行磁共振成像(MRI)以测量T(BBB完整性的标志物)、T(水肿)和脑血流量(CBF)。MRI检查后,处死动物并进行免疫组织化学或蛋白质印迹分析。

结果

与对照组相比,接受辛伐他汀治疗的动物的MRI数据显示,ICH后4天,ICH边缘的BBB功能障碍显著减轻,CBF改善(<0.05)。辛伐他汀还显著降低了ICH后4天边缘的水肿(T)(<0.05)。两个他汀类药物治疗组均显示血管壁内闭合蛋白和内皮屏障抗原水平升高,表明BBB功能得到更好的保留(<0.05),血管数量增加(<0.05)。

结论

ICH后急性给予辛伐他汀治疗可通过MRI和相关免疫组织化学测量保护BBB完整性。MRI也有证据表明CBF改善和水肿减轻。相反,阿托伐他汀在MRI测量中显示出不显著的趋势。