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一种正在进展的大鼠卒中的光血栓形成“环”模型,显示出假定的半暗带反转。

A photothrombotic 'ring' model of rat stroke-in-evolution displaying putative penumbral inversion.

作者信息

Wester P, Watson B D, Prado R, Dietrich W D

机构信息

Department of Neurology, University of Miami, FL 33101.

出版信息

Stroke. 1995 Mar;26(3):444-50. doi: 10.1161/01.str.26.3.444.

Abstract

BACKGROUND AND PURPOSE

To facilitate reproducible and rigorous study of a tissue zone at risk of encroaching ischemic damage, we propose a new model in which the potentially compromised tissue lies within rather than perifocal to an ischemic locus. The perimeter of the "zone at risk" is defined by a photothrombotically produced cortical lesion in the shape of a toroid (or "ring").

METHODS

The exposed crania of erythrosin B-injected rats were irradiated with a 514.5-nm laser beam, configured as a 5-mm-diameter ring, to yield a ring-shaped lesion caused by photochemically induced platelet occlusion of cortical vasculature. Developing perfusion deficits in the interior region were revealed by carbon black infusion. Tissue damage and infarct volumes were assessed by light and electron microscopy, and blood-brain barrier integrity was assessed with Evans blue dye and horseradish peroxidase as tracers.

RESULTS

For rats injected with 17 mg/kg erythrosin B and irradiated for 2 minutes with a ring beam intensity of 0.92 W/cm2 (beam power of 65 mW), carbon black infusion at times up to 4 hours demonstrated a shallow cortical ring lesion encircling a fully patent zone at risk, which by 24 hours evinced an essentially complete perfusion deficit. At times up to 24 hours, the ring lesion was penetrated at the pial surface by distal branches of the middle cerebral and anterior cerebral arteries. Stereotaxically based histopathological assessment showed that by 24 hours the lesion spanned the cortical thickness. Lesion volume increased from 14.5 +/- 8.0 mm3 (mean +/- SD) (n = 8) to 46.2 +/- 15.6 mm3 (n = 8) between 4 and 24 hours after irradiation (P < .01), but the anteroposterior lesion diameter did not change significantly between 4 hours (6.00 +/- 1.03 mm; n = 9) and 24 hours (6.75 +/- 1.15 mm; n = 9).

CONCLUSIONS

The present model of slowly developing but inevitable cortical tissue death in a sequestered area should facilitate more precise observations of the evolution of tissue metabolic responses, from the impending onset of ischemia to the threshold of irreversible damage. This system may prove efficient for evaluating treatments intended to salvage a penumbral region.

摘要

背景与目的

为便于对有遭受缺血性损伤风险的组织区域进行可重复且严谨的研究,我们提出一种新模型,其中潜在受损组织位于缺血灶内部而非周边。“风险区域”的边界由光化学血栓形成的环形(或“环状”)皮质损伤来界定。

方法

用514.5纳米激光束照射注射了赤藓红B的大鼠暴露颅骨,激光束配置为直径5毫米的环形,以产生由光化学诱导的皮质血管血小板阻塞导致的环形损伤。通过注入炭黑揭示内部区域逐渐发展的灌注缺损。通过光镜和电镜评估组织损伤和梗死体积,并用伊文思蓝染料和辣根过氧化物酶作为示踪剂评估血脑屏障完整性。

结果

对于注射17毫克/千克赤藓红B并以0.92瓦/平方厘米的环形光束强度(光束功率65毫瓦)照射2分钟的大鼠,在长达4小时的时间点注入炭黑显示,浅层皮质环形损伤环绕着一个完全通畅的风险区域,到24小时时该区域显示出基本完全的灌注缺损。在长达24小时的时间点,大脑中动脉和大脑前动脉的远端分支在软脑膜表面穿透环形损伤。基于立体定向的组织病理学评估显示,到24小时时损伤跨越皮质全层厚度。照射后4至24小时之间,损伤体积从14.5±8.0立方毫米(平均值±标准差)(n = 8)增加到46.2±15.6立方毫米(n = 8)(P <.01),但损伤的前后径在4小时(6.00±1.03毫米;n = 9)和24小时(6.75±1.15毫米;n = 9)之间无显著变化。

结论

本模型中隔离区域内皮质组织缓慢发展但不可避免的死亡,应有助于更精确地观察从缺血即将发生到不可逆损伤阈值的组织代谢反应演变。该系统可能证明对评估旨在挽救半暗带区域的治疗方法是有效的。

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