用激光散斑血流仪成像视网膜血流。

Frontiers in neuroenergetics Pub Date : 2010-09-15 eCollection Date: 2010-01-01 DOI:10.3389/fnene.2010.00128
Anja I Srienc, Zeb L Kurth-Nelson, Eric A Newman
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引用次数: 76

摘要

激光散斑血流仪(LSF)最初用于测量视网膜中的血流。最近,它的主要应用是成像基线血流量和脑内血流量的活动依赖性变化。我们现在描述了在大鼠视网膜上的实验,其中LSF与共聚焦显微镜一起使用,以监测视网膜血管中光引起的血流变化。这种双重成像技术允许我们用共聚焦显微镜刺激视网膜光感受器和测量血管直径,同时用LSF监测血流。我们发现,闪烁的光会扩张视网膜小动脉,并以相似的时间过程引起视网膜血流速度的增加。此外,聚焦光刺激引起局部血流速度增加。这些增加的空间分布取决于相对于视网膜小动脉和小静脉的刺激位置。结果表明,毛细血管对局部神经元活动无反应,血流动力学反应主要由小动脉介导。使用LSF成像视网膜血流有助于阐明介导视网膜功能性充血的机制,并描述视网膜病理过程中血流的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Imaging retinal blood flow with laser speckle flowmetry.

Imaging retinal blood flow with laser speckle flowmetry.

Imaging retinal blood flow with laser speckle flowmetry.

Imaging retinal blood flow with laser speckle flowmetry.

Laser speckle flowmetry (LSF) was initially developed to measure blood flow in the retina. More recently, its primary application has been to image baseline blood flow and activity-dependent changes in blood flow in the brain. We now describe experiments in the rat retina in which LSF was used in conjunction with confocal microscopy to monitor light-evoked changes in blood flow in retinal vessels. This dual imaging technique permitted us to stimulate retinal photoreceptors and measure vessel diameter with confocal microscopy while simultaneously monitoring blood flow with LSF. We found that a flickering light dilated retinal arterioles and evoked increases in retinal blood velocity with similar time courses. In addition, focal light stimulation evoked local increases in blood velocity. The spatial distribution of these increases depended on the location of the stimulus relative to retinal arterioles and venules. The results suggest that capillaries are largely unresponsive to local neuronal activity and that hemodynamic responses are mediated primarily by arterioles. The use of LSF to image retinal blood flow holds promise in elucidating the mechanisms mediating functional hyperemia in the retina and in characterizing changes in blood flow that occur during retinal pathology.

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