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首页> 外文期刊>Journal of Neuropathology and Experimental Neurology >Reduced Ratio of Afferent to Total Vascular Density in Mesial Temporal Sclerosis
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Reduced Ratio of Afferent to Total Vascular Density in Mesial Temporal Sclerosis

机译:中度颞叶硬化症中传入血管密度与总血管密度的比率降低

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摘要

Mesial temporal sclerosis (MTS) is the most common cause of drug-resistant temporal lobe epilepsy in adults. Despite nearly 2 centuries since the first reports of MTS, relatively little is known about its etiology and pathogenesis. Increasing attention has been directed toward the potential role of vascular abnormalities in MTS. We evaluated the hippocampal microvasculature in 9 MTS cases and 3 non-MTS controls using celloidin tissue sections and markers for total (collagen type IV) and afferent (enzymatic alkaline phosphatase) vessels. Tissue sections were assessed by light microscopy and quantified by threshold analysis of digital images and stereological analysis using the Space Balls probe. Although consistent alterations in the total microvascular density were not found, there was a significant reduction in the density of afferent vessels using both methodologies; these reductions were in areas CA2 and CA3 by image threshold analysis and in area CA3 using stereological measures of the ratio of afferent to total vessels. Increased numbers of string vessels (i.e. remnants of regressing vasculature) were also observed in Ammon's horn, suggesting vascular degeneration in the MTS hippocampus. These findings may help further our understanding of the pathophysiology of MTS.
机译:中间颞叶硬化(MTS)是成年人中耐药性颞叶癫痫的最常见原因。尽管自首次报道MTS以来已有近两个世纪的历史,但对其病因和发病机制知之甚少。人们越来越关注血管异常在MTS中的潜在作用。我们评估了9例MTS病例和3例非MTS对照的海马微脉管系统,并使用了类纤维蛋白组织切片和总(IV型胶原)和传入(酶促碱性磷酸酶)血管的标记物。通过光学显微镜评估组织切片,并通过数字图像的阈值分析和使用Space Balls探针的立体分析进行定量。尽管未发现总微血管密度的一致变化,但两种方法均显着降低了传入血管的密度。这些减少是通过图像阈值分析在CA2和CA3区域中进行的,而在使用传入量与总血管比率的立体测量的CA3区域中的减少。在Ammon的角中也观察到了弦血管数量的增加(即血管退化的残留),这表明MTS海马中的血管变性。这些发现可能有助于我们进一步了解MTS的病理生理。

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    《Journal of Neuropathology and Experimental Neurology》 |2009年第10期|p.1147-1154|共8页
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    Ryan T. Mott, MD, Clara R. Thore, PhD, Dixon M. Moody, MD, Steven S. Glazier, MD, Thomas L. Ellis, MD, and William R. Brown, PhDFrom the Departments of Pathology (RTM, WRB), Radiology (CRT, DMM, WRB), and Neurosurgery (TLE), Wake Forest University School of Medicine, Winston-Salem, North Carolina, Department of Neuroscience (SSG), Division of Neurosurgery, Medical University of South Carolina, Charleston, South Carolina.Send correspondence and reprint requests to: Clara R. Thore, PhD, Microvascular Research Laboratory, Department of Diagnostic Radiology, Wake Forest University School of Medicine, Medical Center Blvd, Winston-Salem, NC 27157, E-mail: cthore@wfubmc.eduThis work was supported by National Institutes of Health Grants NS020618 and CA113321.Online-only color figures are available at http://www.jneuropath.com.,;

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