TY - JOUR
T1 - Reduced ocular blood flow as an early indicator of diabetic retinopathy in a mouse model of diabetes
AU - Muir, Eric R.
AU - Rentería, René C.
AU - Duong, Timothy Q.
N1 - Copyright:
Copyright 2013 Elsevier B.V., All rights reserved.
PY - 2012/9
Y1 - 2012/9
N2 - Purpose. To investigate ocular blood flow and visual function in the Ins2Akita diabetic retinopathy mouse model at early and late time points after onset of hyperglycemia. Methods. Mice heterozygous for the Ins2Akita mutation, which become hyperglycemic at approximately 4 weeks old, were studied at 2.5 and 7.5 months of age, with age-matched wild-type littermates used as controls. Retinal and choroidal blood flows were noninvasively imaged at 42 × 42 × 400 μm using magnetic resonance imaging. Visual function was measured using optokinetic tracking to determine spatial frequency and contrast thresholds from the same mice. Results. At 2.5 months, choroidal blood flow was significantly reduced (P < 0.01) by 20% in Ins2Akita mice (n = 13) compared with age-matched controls (n = 16), whereas retinal blood flow and visual function were not significantly affected (P > 0.05). At 7.5 months, both choroidal and retinal blood flow were significantly reduced (P < 0.05) by 27% and 28%, respectively, in Ins2Akita mice (n = 11) compared with age-matched controls (n = 15). Visual functions were also significantly worse (P < 0.05) in Ins2Akita mice at 7.5 months, as indicated by a 19% decreased spatial frequency threshold and 135% increased contrast threshold compared with age-matched controls. The magnitudes of the blood flow and vision deficits, however, were not correlated. Conclusions. Although both choroidal and retinal blood flow and vision were altered after prolonged diabetes in the Ins2Akita mouse, choroidal blood flow was reduced even in young diabetic animals, suggesting ocular blood flow deficit could be an early pathological change in diabetic retinopathy.
AB - Purpose. To investigate ocular blood flow and visual function in the Ins2Akita diabetic retinopathy mouse model at early and late time points after onset of hyperglycemia. Methods. Mice heterozygous for the Ins2Akita mutation, which become hyperglycemic at approximately 4 weeks old, were studied at 2.5 and 7.5 months of age, with age-matched wild-type littermates used as controls. Retinal and choroidal blood flows were noninvasively imaged at 42 × 42 × 400 μm using magnetic resonance imaging. Visual function was measured using optokinetic tracking to determine spatial frequency and contrast thresholds from the same mice. Results. At 2.5 months, choroidal blood flow was significantly reduced (P < 0.01) by 20% in Ins2Akita mice (n = 13) compared with age-matched controls (n = 16), whereas retinal blood flow and visual function were not significantly affected (P > 0.05). At 7.5 months, both choroidal and retinal blood flow were significantly reduced (P < 0.05) by 27% and 28%, respectively, in Ins2Akita mice (n = 11) compared with age-matched controls (n = 15). Visual functions were also significantly worse (P < 0.05) in Ins2Akita mice at 7.5 months, as indicated by a 19% decreased spatial frequency threshold and 135% increased contrast threshold compared with age-matched controls. The magnitudes of the blood flow and vision deficits, however, were not correlated. Conclusions. Although both choroidal and retinal blood flow and vision were altered after prolonged diabetes in the Ins2Akita mouse, choroidal blood flow was reduced even in young diabetic animals, suggesting ocular blood flow deficit could be an early pathological change in diabetic retinopathy.
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U2 - 10.1167/iovs.12-9758
DO - 10.1167/iovs.12-9758
M3 - Article
C2 - 22915034
AN - SCOPUS:84871898419
VL - 53
SP - 6488
EP - 6494
JO - Investigative Ophthalmology and Visual Science
JF - Investigative Ophthalmology and Visual Science
SN - 0146-0404
IS - 10
ER -