Suppr超能文献

血管痉挛对蛛网膜下腔出血大鼠模型中血红素加氧酶的影响。

Effect of vasospasm on heme oxygenases in a rat model of subarachnoid hemorrhage.

作者信息

Kuroki M, Kanamaru K, Suzuki H, Waga S, Semba R

机构信息

Department of Neurosurgery, Mie University School of Medicine, Tsu, Japan.

出版信息

Stroke. 1998 Mar;29(3):683-8; discussion 688-9. doi: 10.1161/01.str.29.3.683.

Abstract

BACKGROUND AND PURPOSE

Subarachnoid hemorrhage (SAH)-induced heme oxygenase-1 (HO-1) in glia throughout the rat brain without affecting heme oxygenase-2 (HO-2). However, the relationship between cerebral vasospasm and the expression of heme oxygenases after SAH is thus far unknown. The purpose of the present study was to clarify the effect of vasospasm on the expression of heme oxygenases in a rat model of SAH.

METHODS

Endothelin, hemolysate, hemolysate saturated with carbon monoxide (CO-hemolysate), and saline were injected into the cisterna magna of adult rats. Angiography was repeated before each injection and 15 and 60 minutes and 24 hours after each injection. Immunocytochemistry for HO-1, HO-2, and glial fibrillary acidic protein (GFAP) was performed 24 hours after the injection.

RESULTS

A significant vasospasm occurred in the basilar artery after the injection of endothelin, hemolysate, and CO-hemolysate. The degree of vasospasm was most prominent 15 minutes after each injection. There was no significant difference in the degree of vasospasm among injections. The HO-1 was induced exclusively in the glial cells throughout the brain after injection of hemolysate and CO-hemolysate; however, it was not induced by endothelin and saline. In the dentate gyrus of the hippocampus and the molecular layer of the cerebellum, the HO-1-positive cells were also stained for GFAP, suggesting astrocytic glial cells. On the other hand, HO-2 immunoreactivity was abundant in neurons and was not affected by endothelin, hemolysate, CO-hemolysate, or saline.

CONCLUSIONS

It is suggested that heme per se, rather than ischemia induced by vasospasm, plays a pivotal role in the expression of HO-1 in this rat model.

摘要

背景与目的

蛛网膜下腔出血(SAH)可诱导大鼠全脑胶质细胞中的血红素加氧酶-1(HO-1),而不影响血红素加氧酶-2(HO-2)。然而,SAH后脑血管痉挛与血红素加氧酶表达之间的关系至今尚不清楚。本研究的目的是阐明血管痉挛对SAH大鼠模型中血红素加氧酶表达的影响。

方法

将内皮素、溶血产物、一氧化碳饱和溶血产物(CO-溶血产物)和生理盐水注入成年大鼠的小脑延髓池。在每次注射前以及每次注射后15分钟、60分钟和24小时重复进行血管造影。注射后24小时进行HO-1、HO-2和胶质纤维酸性蛋白(GFAP)的免疫细胞化学检测。

结果

注射内皮素、溶血产物和CO-溶血产物后基底动脉出现明显的血管痉挛。每次注射后15分钟血管痉挛程度最为显著。各次注射之间血管痉挛程度无显著差异。注射溶血产物和CO-溶血产物后,HO-1仅在全脑的胶质细胞中被诱导;然而,内皮素和生理盐水未诱导其表达。在海马齿状回和小脑分子层,HO-1阳性细胞也被GFAP染色,提示为星形胶质细胞。另一方面,HO-2免疫反应性在神经元中丰富,且不受内皮素、溶血产物、CO-溶血产物或生理盐水的影响。

结论

提示在该大鼠模型中,血红素本身而非血管痉挛诱导的缺血在HO-1的表达中起关键作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验