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易卒中型自发性高血压大鼠高血压前的脑小血管内皮结构改变:对 5 至 21 周龄大鼠进行的一项盲法、对照免疫组织化学研究。

Cerebral small vessel endothelial structural changes predate hypertension in stroke-prone spontaneously hypertensive rats: a blinded, controlled immunohistochemical study of 5- to 21-week-old rats.

机构信息

Division of Clinical Neurosciences Centre for Molecular Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, UK.

出版信息

Neuropathol Appl Neurobiol. 2011 Dec;37(7):711-26. doi: 10.1111/j.1365-2990.2011.01170.x.

Abstract

AIMS

The spontaneously hypertensive stroke-prone rat (SHRSP) is a potential animal model of human lacunar stroke, but there is little information on SHRSP small vessel pathology, especially in young rats. We investigated the structural changes that occur in cortical and subcortical vessels and adjacent tissue in SHRSP before, during and after the onset of hypertension.

METHODS

We examined brains from SHRSP and Wistar Kyoto rats (WKY) at 5, 16 and 21 weeks of age. Structural changes in small arterioles and adjacent tissue were studied using antibodies to investigate different components of the neurovascular unit. We quantified staining in three standard regions, at two coronal levels.

RESULTS

Immunostaining for claudin-5, a marker of endothelial tight junctions, was reduced in SHRSP at all ages compared to age-matched WKY controls. Smooth muscle actin, glial fibrillary acidic protein and ionized calcium-binding adaptor molecule 1 were increased in SHRSP vs. WKY by 16 weeks. Additionally, 21-week-old WKY and SHRSP rats fed a high-salt diet showed differences in claudin-5, glial fibrillary acidic protein and matrix metalloproteinase 9 staining compared to those fed a normal diet.

CONCLUSION

Endothelial tight junction alterations of SHRSP rats from the earliest ages point towards increased susceptibility to blood-brain barrier dysfunction and stroke, which is exacerbated by salt loading. Salt loading may also damage the neurovascular unit in WKY controls.

摘要

目的

自发性高血压卒中易发性大鼠(SHRSP)是人类腔隙性卒中的潜在动物模型,但关于 SHRSP 小血管病理学的信息很少,尤其是在幼鼠中。我们研究了在高血压发生之前、期间和之后,SHRSP 皮质和皮质下血管及邻近组织中发生的结构变化。

方法

我们在 5、16 和 21 周龄时检查了 SHRSP 和 Wistar 京都大鼠(WKY)的大脑。使用针对神经血管单元不同成分的抗体研究小动脉和邻近组织的结构变化。我们在两个冠状平面的三个标准区域定量了染色。

结果

与同龄 WKY 对照组相比,所有年龄的 SHRSP 中紧密连接标志物闭合蛋白-5的免疫染色均减少。平滑肌肌动蛋白、胶质纤维酸性蛋白和钙结合衔接分子 1 在 SHRSP 中比 WKY 增加了 16 周。此外,21 周龄的 SHRSP 和 WKY 大鼠在高盐饮食组中与正常饮食组相比,闭合蛋白-5、胶质纤维酸性蛋白和基质金属蛋白酶 9 的染色存在差异。

结论

从最早的年龄开始,SHRSP 大鼠的内皮紧密连接改变表明其对血脑屏障功能障碍和卒中的易感性增加,盐负荷会加剧这种情况。盐负荷也可能损害 WKY 对照组的神经血管单元。

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