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内皮糖萼对小鼠脑血流的影响。

Influence of the endothelial glycocalyx on cerebral blood flow in mice.

作者信息

Vogel J, Sperandio M, Pries A R, Linderkamp O, Gaehtgens P, Kuschinsky W

机构信息

Department of Physiology and Pathophysiology, University of Heidelberg, Germany.

出版信息

J Cereb Blood Flow Metab. 2000 Nov;20(11):1571-8. doi: 10.1097/00004647-200011000-00007.

DOI:10.1097/00004647-200011000-00007
PMID:11083232
Abstract

The endothelial surface layer (glycocalyx) of cerebral capillaries may increase resistance to blood flow. This hypothesis was investigated in mice by intravenous administration of heparinase (2500 IU/kg body weight in saline), which cleaves proteoglycan junctions of the glycocalyx. Morphology was investigated by transmission electron microscopy. Cerebral perfusion velocity was recorded before and during heparinase or saline treatment using laser-Doppler flowmetry. In addition, cerebral blood flow (CBF) was measured 10 minutes after heparinase or saline treatment using the iodo[14C]antipyrine method. Laser-Doppler flowmetry and CBF measurements were performed during normocapnia and severe hypercapnia (PCO2: 120 mm Hg). After heparinase, morphology showed a reduced thickness of the glycocalyx in cortical microvessels by 43% (P < 0.05) compared with saline-treated controls. Under normocapnic conditions, a 15% (P < 0.05) transient increase of cerebral flow velocity occurred 2.5 to 5 minutes after heparinase injection. Laser-Doppler flow and CBF returned to control values ten minutes after the injection. However, during severe hypercapnia, heparinase treatment resulted in a persisting increase in laser-Doppler flow (6%, P < 0.05) and CBF (30%, P < 0.05). These observations indicate the existence of a flow resistance in cerebral capillaries exerted by the glycocalyx. The transient nature of the CBF increase during normocapnia may be explained by a vascular compensation that is exhausted during severe hypercapnia.

摘要

脑毛细血管的内皮表面层(糖萼)可能会增加血流阻力。本研究通过给小鼠静脉注射肝素酶(2500 IU/kg体重,溶于生理盐水)来验证这一假设,肝素酶可裂解糖萼的蛋白聚糖连接。通过透射电子显微镜研究形态学变化。使用激光多普勒血流仪记录肝素酶或生理盐水处理前及处理过程中的脑灌注速度。此外,在肝素酶或生理盐水处理10分钟后,使用碘[14C]安替比林法测量脑血流量(CBF)。在正常碳酸血症和严重高碳酸血症(PCO2:120 mmHg)期间进行激光多普勒血流仪测量和CBF测量。注射肝素酶后,与生理盐水处理的对照组相比,形态学显示皮质微血管中糖萼厚度减少了43%(P < 0.05)。在正常碳酸血症条件下,注射肝素酶后2.5至5分钟,脑血流速度出现15%的短暂增加(P < 0.05)。注射10分钟后,激光多普勒血流和CBF恢复到对照值。然而,在严重高碳酸血症期间,肝素酶处理导致激光多普勒血流持续增加(6%,P < 0.05)和CBF持续增加(30%,P < 0.05)。这些观察结果表明糖萼在脑毛细血管中产生了血流阻力。正常碳酸血症期间CBF增加的短暂性可能是由于血管代偿作用,而在严重高碳酸血症期间这种代偿作用耗尽。

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