Harris et al. [2] also provided evidence of the presence of
retinal hypoxia in the early stages of diabetes by showing that contrast sensitivity was improved when patients with early diabetic retinopathy were made hyperoxic.
Not exact matches
The expression of a few
retinal mRNAs known to be induced by
hypoxia, including HIF - 1α, was assessed by qRT — PCR analysis of total RNA isolated from
retinal tissue following exposure to 3 h of 6 % — 7 % O2.
In most cases,
hypoxia is caused by either a dysfunction of the
retinal vasculature, as in diabetic retinopathy and
retinal artery and vein occlusions, or it is due to a mismatch between nutrient supply and demand, as in the case of a
retinal detachment, where the retina is separated too far from the choroid to receive sufficient oxygen.
Insight into the novel role that NMDA receptors play in
retinal responses to
hypoxia may be derived from study of the coordinated expression patterns of genes that interact, either directly or indirectly, with the NMDA receptor; namely, the NMDA interactome.
Chronic experimental
hypoxia kills photoreceptors in adult rat retina [14] and can lead to
retinal angiogenesis [15].
Conclusions: The identification of gene expression alterations as a function of
hypoxia and recovery from
hypoxia is important to understand the molecular mechanisms underlying
retinal dysfunction associated with a variety of diseases.
Little is known about the molecular effects of
hypoxia on the retina and the underlying relationship between
hypoxia and the pathogenesis of
retinal diseases.
Some evidence of the involvement of
retinal tissue
hypoxia has come from in vivo measurements in animal models of disease, though the onset of
hypoxia and the severity of the insult have been difficult to identify.
Park, Y. S., Kim, N. H. & Jo, I.
Hypoxia and vascular endothelial growth factor acutely up - regulate angiopoietin - 1 and Tie2 mRNA in bovine
retinal pericytes.