Department of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV, 89557-0318, USA.
Department of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV, 89557-0318, USA.
Exp Eye Res. 2023 Aug;233:109543. doi: 10.1016/j.exer.2023.109543. Epub 2023 Jun 28.
Several hypotheses have been tested to understand whole organ regulation in other organs such as the brain and kidney, but no such hypothesis has yet been proposed for ocular circulations. To some extent resolve this deficit our ex vivo mouse eye perfusion model takes the first step in elucidating the mechanisms controlling the individual components of the ocular circulation. Various isolated ocular vascular preparations have been utilized in studies of ocular vascular biology, physiology, and pharmacology, including studies on both normal and pathological conditions. However, there is still significant potential for further studies to improve our understanding of ocular circulation and its regulation. The choroid specifically is inaccessible to direct visualization due to the retina's high metabolic requirement with a transparency that cannot be compromised by an overly rich vascular network on the inner retinal side hindering the visualization of the choroid. In this technical paper, we provide a detailed description of all the steps to be followed from the enucleation of mouse eyes to cannulation of the ophthalmic artery and perfusion and ex vivo confocal microscopy imaging of the dynamic nature of the choroid circulation.
已经提出了一些假设来理解大脑和肾脏等其他器官的整体器官调节,但对于眼部循环还没有提出这样的假设。为了在一定程度上解决这一不足,我们的离体小鼠眼灌注模型在阐明控制眼部循环各个组成部分的机制方面迈出了第一步。各种离体眼部血管制剂已被用于眼部血管生物学、生理学和药理学的研究,包括正常和病理条件下的研究。然而,仍然有很大的潜力进行进一步的研究,以提高我们对眼部循环及其调节的理解。脉络膜特别难以直接可视化,因为视网膜的高代谢需求和透明度使得脉络膜的血管网络过于丰富而无法妥协,这会阻碍脉络膜的可视化。在本技术论文中,我们详细描述了从眼球取出到眼球动脉插管、灌注和离体共聚焦显微镜成像的所有步骤,以观察脉络膜循环的动态性质。