TY - JOUR
T1 - Monitoring retinal responses to acute intraocular pressure elevation in rats with visible light optical coherence tomography
AU - Pi, Shaohua
AU - Hormel, Tristan T.
AU - Wei, Xiang
AU - Cepurna, William
AU - Camino, Acner
AU - Guo, Yukun
AU - Huang, David
AU - Morrison, John
AU - Jia, Yali
N1 - Funding Information:
This work was supported by Grant Nos. R01 EY027833, DP3 DK104397, R01 EY024544, R01 EY023285, R01 EY010145, and P30 EY010572 from the National Institutes of Health (Bethesda, Maryland), an unrestricted departmental funding grant, and a William & Mary Greve Special Scholar Award from Research to Prevent Blindness (New York, New York).
Publisher Copyright:
© The Authors. Published by SPIE under a Creative Commons Attribution 4.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI.
PY - 2019/10/1
Y1 - 2019/10/1
N2 - Elevated intraocular pressure (IOP) is an important risk factor for glaucoma. However, the role of IOP in glaucoma progression, as well as retinal physiology in general, remains incompletely understood. We demonstrate the use of visible light optical coherence tomography to measure retinal responses to acute IOP elevation in Brown Norway rats. We monitored retinal responses in reflectivity, angiography, blood flow, oxygen saturation (sO2), and oxygen metabolism over a range of IOP from 10 to 100 mmHg. As IOP was elevated, nerve fiber layer reflectivity was found to decrease. Vascular perfusion in the three retinal capillary plexuses remained steady until IOP exceeded 70 mmHg and arterial flow was noted to reverse periodically at high IOPs. However, a significant drop in total retinal blood flow was observed first at 40 mmHg. As IOP increased, the venous sO2 demonstrated a gradual decrease despite steady arterial sO2, which is consistent with increased arterial-venous oxygen extraction across the retinal capillary beds. Calculated total retinal oxygen metabolism was steady, reflecting balanced responses of blood flow and oxygen extraction, until IOP exceeded 40 mmHg, and fell to 0 at 70 and 80 mmHg. Above this, measurements were unattainable. All measurements reverted to baseline when the IOP was returned to 10 mmHg, indicating good recovery following acute pressure challenge. These results demonstrate the ability of this system to monitor retinal oxygen metabolism noninvasively and how it can help us understand retinal responses to elevated IOP.
AB - Elevated intraocular pressure (IOP) is an important risk factor for glaucoma. However, the role of IOP in glaucoma progression, as well as retinal physiology in general, remains incompletely understood. We demonstrate the use of visible light optical coherence tomography to measure retinal responses to acute IOP elevation in Brown Norway rats. We monitored retinal responses in reflectivity, angiography, blood flow, oxygen saturation (sO2), and oxygen metabolism over a range of IOP from 10 to 100 mmHg. As IOP was elevated, nerve fiber layer reflectivity was found to decrease. Vascular perfusion in the three retinal capillary plexuses remained steady until IOP exceeded 70 mmHg and arterial flow was noted to reverse periodically at high IOPs. However, a significant drop in total retinal blood flow was observed first at 40 mmHg. As IOP increased, the venous sO2 demonstrated a gradual decrease despite steady arterial sO2, which is consistent with increased arterial-venous oxygen extraction across the retinal capillary beds. Calculated total retinal oxygen metabolism was steady, reflecting balanced responses of blood flow and oxygen extraction, until IOP exceeded 40 mmHg, and fell to 0 at 70 and 80 mmHg. Above this, measurements were unattainable. All measurements reverted to baseline when the IOP was returned to 10 mmHg, indicating good recovery following acute pressure challenge. These results demonstrate the ability of this system to monitor retinal oxygen metabolism noninvasively and how it can help us understand retinal responses to elevated IOP.
KW - Functional monitoring and imaging
KW - Glaucoma
KW - Optical coherence tomography
KW - Oxygen metabolism
KW - Total retinal blood flow
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U2 - 10.1117/1.NPh.6.4.041104
DO - 10.1117/1.NPh.6.4.041104
M3 - Article
AN - SCOPUS:85069502479
SN - 2329-423X
VL - 6
JO - Neurophotonics
JF - Neurophotonics
IS - 4
M1 - 041104
ER -