Abstract
Oxygen-sensitive microelectrodes were used to measure the intraretinal oxygen distribution in the rat during both air and oxygen breathing. During air breathing the average PO 2 profile obtained showed a value of 19 ± 2.5 mmHg (n = 36) at the internal limiting membrane (ILM). As the penetration depth increased, a minimal PO 2 of 8.2±2.4 mmHg was attained at 50% of the retinal depth, from which point the PO 2 increased to a peak of 33 ± 3.3 mmHg at 100% of the retinal depth at Bruch's membrane. During oxygen ventilation, all intraretinal oxygen tensions were increased and the profile became almost monotonic, increasing from 36.1 ±3.3 mmHg (n = 9) at the ILM to 134.3 ± 6.7 mmHg at 100% of the retinal depth. These results are qualitatively similar to those found in the cat, and they demonstrate the importance of oxygen delivery by both the retinal and the choroidal circulation during normoxia, as well as the inability of vascular autoregulation to maintain a constant retinal P02 during hyperoxic ventilation.
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This work was supported by the Juvenile Diabetes Foundation International, the Medical Research Fund of Western Australia, TVW Telethon, the Clive and Vera Ramaciotti Foundation, and the National Health and Medical Research Council of Australia
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Cringle, S.J., Yu, DY. & Alder, V.A. Intraretinal oxygen tension in the rat eye. Graefe's Arch Clin Exp Ophthalmol 229, 574–577 (1991). https://doi.org/10.1007/BF00203324
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DOI: https://doi.org/10.1007/BF00203324