TY - JOUR
T1 - Retinal oxygen tension and the electroretinogram during arterial occlusion in the cat
AU - Braun, R. D.
AU - Linsenmeier, Robert A
PY - 1995/1/1
Y1 - 1995/1/1
N2 - Purpose. Retinal oxygen tension (PO2), photoreceptor oxygen consumption (QO2), the local electroretinogram (LERG), and the vitreally recorded electroretinogram (ERG) were evaluated during retinal artery occlusion in the cat. The feasibility of supplying the retina with oxygen during occlusion by ventilation with 100% O2 was evaluated. Methods. Double-barreled oxygen microelectrodes were used to measure intraretinal PO2 and LERGs in anesthetized cats before, during, and alter occlusion of a single retinal artery. Outer retinal (photoreceptor) QO2 was determined from retinal PO2 profiles. Results. During air breathing, occlusion obliterated the LERG b- wave and reduced the vitreal ERG by the amount expected from the area supplied by the occluded vessel. The PO2 in the entire inner retina was zero, and photoreceptor QO2 was decreased by approximately 25%. Inspiration of 100% O2 restored the b-wave amplitude to approximately 50% of normal and increased the amount of O2 reaching the inner retina. Hyperoxia could not guarantee nonzero PO2 across the entire retina in either darkness or light, but it elevated the average PO2 in the innermost 25% of the retina to more than 20 mm Hg. The b-wave amplitude must have been affected by some factor in addition to local hypoxia, because the amplitude was not correlated with inner retinal PO2 during occlusion, and a normal PO2 did not result in a normal LERG. Effects of 2 to 2.5 hours of occlusion were reversible if 100% O2 inspiration was maintained during most of the occlusion. Conclusions. Ventilation with 100% O2 during occlusion increased the PO2 across most of the retina and partially restored the LERG b-wave, but the tissue near the vitreous was still sometimes anoxic. The illumination status seemed to make little difference. Inspiration of elevated O2 might be beneficial in treating retinal vascular occlusive disease, although it alone cannot completely maintain retinal function.
AB - Purpose. Retinal oxygen tension (PO2), photoreceptor oxygen consumption (QO2), the local electroretinogram (LERG), and the vitreally recorded electroretinogram (ERG) were evaluated during retinal artery occlusion in the cat. The feasibility of supplying the retina with oxygen during occlusion by ventilation with 100% O2 was evaluated. Methods. Double-barreled oxygen microelectrodes were used to measure intraretinal PO2 and LERGs in anesthetized cats before, during, and alter occlusion of a single retinal artery. Outer retinal (photoreceptor) QO2 was determined from retinal PO2 profiles. Results. During air breathing, occlusion obliterated the LERG b- wave and reduced the vitreal ERG by the amount expected from the area supplied by the occluded vessel. The PO2 in the entire inner retina was zero, and photoreceptor QO2 was decreased by approximately 25%. Inspiration of 100% O2 restored the b-wave amplitude to approximately 50% of normal and increased the amount of O2 reaching the inner retina. Hyperoxia could not guarantee nonzero PO2 across the entire retina in either darkness or light, but it elevated the average PO2 in the innermost 25% of the retina to more than 20 mm Hg. The b-wave amplitude must have been affected by some factor in addition to local hypoxia, because the amplitude was not correlated with inner retinal PO2 during occlusion, and a normal PO2 did not result in a normal LERG. Effects of 2 to 2.5 hours of occlusion were reversible if 100% O2 inspiration was maintained during most of the occlusion. Conclusions. Ventilation with 100% O2 during occlusion increased the PO2 across most of the retina and partially restored the LERG b-wave, but the tissue near the vitreous was still sometimes anoxic. The illumination status seemed to make little difference. Inspiration of elevated O2 might be beneficial in treating retinal vascular occlusive disease, although it alone cannot completely maintain retinal function.
UR - http://www.scopus.com/inward/record.url?scp=0028944692&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0028944692&partnerID=8YFLogxK
M3 - Article
C2 - 7890484
AN - SCOPUS:0028944692
SN - 0146-0404
VL - 36
SP - 523
EP - 541
JO - Investigative Ophthalmology and Visual Science
JF - Investigative Ophthalmology and Visual Science
IS - 3
ER -