Literature DB >> 11053305

Intraretinal oxygen levels before and after photoreceptor loss in the RCS rat.

D Y Yu1, S J Cringle, E N Su, P K Yu.   

Abstract

PURPOSE: To measure the intraretinal oxygen environment at different stages in the Royal College of Surgeons (RCS) rat model of retinal degeneration to determine whether changes in oxygen level are an important aspect of the disease.
METHODS: Oxygen-sensitive microelectrodes were used to measure oxygen tension as a function of depth through the retina of anesthetized, mechanically ventilated RCS rats at ages ranging from postnatal day (P)20 to P104. The oxygen profiles were correlated with histologic observations of the cellular changes within the dystrophic retinas and compared with those in RCS-rdy(+) control animals and published values in normal mature rats.
RESULTS: Although the youngest rats studied exhibited some differences in intraretinal oxygen distribution compared with mature animals, the distribution in dystrophic RCS rats at P20 was not significantly different from that in age-matched control subjects. However, the intraretinal oxygen distribution in dystrophic RCS rats was clearly affected after approximately P30, reflecting a loss of photoreceptor oxygen consumption consistent with histologic observations. In contrast, oxygen uptake by the inner retina was still evident long after the loss of photoreceptors was essentially complete.
CONCLUSIONS: There was no significant tissue hypoxia during photoreceptor degeneration in the dystrophic RCS rat. The changes in intraretinal oxygen distribution are consistent with the loss of outer retinal oxygen uptake but the preservation of inner retinal oxygen metabolism.

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Year:  2000        PMID: 11053305

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  63 in total

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Journal:  Invest Ophthalmol Vis Sci       Date:  2010-06       Impact factor: 4.799

2.  Layer-specific blood-flow MRI of retinitis pigmentosa in RCS rats.

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3.  Long-term expression of glial cell line-derived neurotrophic factor slows, but does not stop retinal degeneration in a model of retinitis pigmentosa.

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4.  Cone degeneration following rod ablation in a reversible model of retinal degeneration.

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5.  NADPH oxidase plays a central role in cone cell death in retinitis pigmentosa.

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6.  Cell metabolism: Sugar for sight.

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7.  Blood flow magnetic resonance imaging of retinal degeneration.

Authors:  Yingxia Li; Haiying Cheng; Qiang Shen; Moon Kim; Peter M Thule; Darin E Olson; Machelle T Pardue; Timothy Q Duong
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-10-24       Impact factor: 4.799

8.  Increased expression of catalase and superoxide dismutase 2 reduces cone cell death in retinitis pigmentosa.

Authors:  Shinichi Usui; Keiichi Komeima; Sun Young Lee; Young-Joon Jo; Shinji Ueno; Brian S Rogers; Zhihao Wu; Jikui Shen; Lili Lu; Brian C Oveson; Peter S Rabinovitch; Peter A Campochiaro
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9.  Increased expression of glutathione peroxidase 4 strongly protects retina from oxidative damage.

Authors:  Lili Lu; Brain C Oveson; Young-Joon Jo; Thomas W Lauer; Shinichi Usui; Keiichi Komeima; Bing Xie; Peter A Campochiaro
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Review 10.  Magnetic resonance imaging of the retina: from mice to men.

Authors:  Timothy Q Duong
Journal:  Magn Reson Med       Date:  2013-05-28       Impact factor: 4.668

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