PURPOSE: To investigate oxygen tension (P(O2)) changes in the retinal and choroidal vasculatures in response to visual stimulation by light flicker. METHODS: A previously developed optical section phosphorescence imaging system was used to measure P(O2) separately in the retinal veins, arteries, and capillaries and in the choroid before and during light flicker. Imaging was performed in rats during light flicker at frequencies between 0 and 14 Hz. Light flicker-induced changes in the chorioretinal vasculature P(O2) and arteriovenous P(O2) differences were determined. Retinal arterial and venous P(O2) were measured along blood vessels as a function of the distance from the optic nerve head. RESULTS: Retinal arterial P(O2) and arteriovenous P(O2) differences increased with increasing light flicker at frequencies up to 10 Hz, after which no further increase was observed. Significant increases in retinal arterial P(O2) (P = 0.009; n =10) and in retinal capillary P(O2) (P = 0.04, n = 10) were measured in response to light flicker at 10 Hz. Retinal arteriovenous P(O2) differences during light flicker were significantly greater than differences before light flicker (P = 0.01; n = 10). Retinal arterial P(O2) decreased significantly with increased distance from the optic nerve head (P < or = 0.004), whereas retinal venous P(O2) remained relatively unchanged (P > or= 0.4). CONCLUSIONS: Measurement of changes in the chorioretinal vasculature P(O2) can potentially advance the understanding of oxygen dynamics in challenged physiological states and in animal models of human retinal diseases.
PURPOSE: To investigate oxygen tension (P(O2)) changes in the retinal and choroidal vasculatures in response to visual stimulation by light flicker. METHODS: A previously developed optical section phosphorescence imaging system was used to measure P(O2) separately in the retinal veins, arteries, and capillaries and in the choroid before and during light flicker. Imaging was performed in rats during light flicker at frequencies between 0 and 14 Hz. Light flicker-induced changes in the chorioretinal vasculature P(O2) and arteriovenous P(O2) differences were determined. Retinal arterial and venous P(O2) were measured along blood vessels as a function of the distance from the optic nerve head. RESULTS:Retinal arterial P(O2) and arteriovenous P(O2) differences increased with increasing light flicker at frequencies up to 10 Hz, after which no further increase was observed. Significant increases in retinal arterial P(O2) (P = 0.009; n =10) and in retinal capillary P(O2) (P = 0.04, n = 10) were measured in response to light flicker at 10 Hz. Retinal arteriovenous P(O2) differences during light flicker were significantly greater than differences before light flicker (P = 0.01; n = 10). Retinal arterial P(O2) decreased significantly with increased distance from the optic nerve head (P < or = 0.004), whereas retinal venous P(O2) remained relatively unchanged (P > or= 0.4). CONCLUSIONS: Measurement of changes in the chorioretinal vasculature P(O2) can potentially advance the understanding of oxygen dynamics in challenged physiological states and in animal models of humanretinal diseases.
Authors: Yen-Yu I Shih; Bryan H De la Garza; Eric R Muir; William E Rogers; Joseph M Harrison; Jeffrey W Kiel; Timothy Q Duong Journal: Invest Ophthalmol Vis Sci Date: 2011-07-15 Impact factor: 4.799
Authors: Yen-Yu I Shih; Lin Wang; Bryan H De La Garza; Guang Li; Grant Cull; Jeffery W Kiel; Timothy Q Duong Journal: Curr Eye Res Date: 2013-01-14 Impact factor: 2.424
Authors: Jesse Schallek; Hongbin Li; Randy Kardon; Young Kwon; Michael Abramoff; Peter Soliz; Daniel Ts'o Journal: Invest Ophthalmol Vis Sci Date: 2009-05-06 Impact factor: 4.799