Dept. of Ophthalmology, Moran Eye Center, University of Utah, 65 Mario Capecchi Dr., Salt Lake City, UT, 84132, United States.
Rocky Vista University College of Osteopathic Medicine, 255 E. Center St. Ivins, UT, 84738, United States.
Exp Eye Res. 2019 Jan;178:91-98. doi: 10.1016/j.exer.2018.09.017. Epub 2018 Sep 27.
Optical coherence tomography (OCT) angiography is a dye-free and non-invasive angiography which allows visualization of retinal and choroid vascular flow, enabling observation of highly permeable and three dimensional vasculature. Although OCT angiography is providing new insights in human retinal and choroidal diseases, a few studies have been reported in experimental mice. In this study, to determine the potential of OCT angiography in experimental mice, we sought to examine whether OCT angiography can detect vascular change in type I diabetic mice. To conduct age dependent analysis, 2 and 6 month old male type 1 diabetic Ins2 and age matched C57BL/6J mice were used. OCT angiography was performed by Heidelberg Spectralis OCT Angiography Module with 30° lens + mouse adapter lens. We acquired the OCT angiography image from the peripheral nasal position. For analysis of OCT angiography images, OCT angiography positive area were used for vascular density. We analyzed vascular density from the retinal surface (inner limiting membrane) to 120 μm depth with 4 μm steps in order to correlate vascular density vs depth (N = 4 per group). Vascular density of both mouse strains demonstrated three different peaks. By comparing with the OCT image, the first peak (superficial), second peak (intermediate) and third peak (deep) were located in nerve fiber layer/ganglion cell layer, inner plexiform layer/inner nuclear layer and outer plexiform layer/outer nuclear layer, respectively. We calculated vascular density of these peaks separately. In C57BL/6J mice, the vascular density in all three layers do not show significant difference between 2- and 6-month-old. On the other hand, 6-month-old Ins2 mice showed a significant decrease of the vascular density in all three layers compared to 2-month-old Ins2 mice. Also, the vascular density of 6-month-old Ins2 mice in the deep layer showed a significant decrease compared to 2- and 6-month-old C57BL/6J mice. Thus, OCT angiography successfully detects retinal vascular difference between type I diabetic mice and control mice, and age-dependent vasculature change in type I diabetic mice. The diabetic mice demonstrated reduced vascular density due to reduced density of flowing deep vessels. Importantly, we observed this difference without retinal blood leakage, hemorrhage or neovascularization. Our analysis (vascular density vs retinal depth) suggests that OCT angiography is useful for in vivo detection of retinal vasculature alteration in experimental mice.
光学相干断层扫描血管造影术(OCT 血管造影术)是一种无需染料的非侵入性血管造影术,可用于观察视网膜和脉络膜血管的血流,使高通透性和三维血管成像成为可能。尽管 OCT 血管造影术在人类视网膜和脉络膜疾病的研究中提供了新的见解,但在实验小鼠中仅有少数研究报道。在这项研究中,为了确定 OCT 血管造影术在实验小鼠中的潜力,我们试图检测 OCT 血管造影术是否可以检测到 1 型糖尿病小鼠的血管变化。为了进行年龄依赖性分析,我们使用 2 个月和 6 个月大的雄性 1 型糖尿病 Ins2 小鼠和年龄匹配的 C57BL/6J 小鼠。使用 Heidelberg Spectralis OCT Angiography Module 结合 30°镜头和小鼠适配器镜头进行 OCT 血管造影。我们从周边鼻侧位置采集 OCT 血管造影图像。为了分析 OCT 血管造影图像,我们使用 OCT 血管造影阳性区域来计算血管密度。我们从视网膜表面(内界膜)到 120 μm 的深度以 4 μm 的步长分析血管密度,以将血管密度与深度相关联(每组 4 只)。两种小鼠品系的血管密度均显示出三个不同的峰值。通过与 OCT 图像比较,第一个峰值(浅层)、第二个峰值(中层)和第三个峰值(深层)分别位于神经纤维层/节细胞层、内丛状层/内核层和外丛状层/外核层。我们分别计算了这些峰值的血管密度。在 C57BL/6J 小鼠中,2 个月和 6 个月大时,所有三层的血管密度没有显著差异。另一方面,与 2 个月大的 Ins2 小鼠相比,6 个月大的 Ins2 小鼠的所有三层的血管密度均显著降低。此外,与 2 个月和 6 个月大的 C57BL/6J 小鼠相比,6 个月大的 Ins2 小鼠深层的血管密度也显著降低。因此,OCT 血管造影术成功地检测到 1 型糖尿病小鼠与对照小鼠之间的视网膜血管差异,以及 1 型糖尿病小鼠的年龄依赖性血管变化。糖尿病小鼠由于深层血流密度降低而导致血管密度降低。重要的是,我们在没有视网膜出血、出血或新生血管形成的情况下观察到了这种差异。我们的分析(血管密度与视网膜深度的关系)表明,OCT 血管造影术对于检测实验小鼠视网膜血管变化是有用的。