2019
DOI: 10.1016/j.aanat.2019.06.007
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Age-related changes of the human retinal vessels: Possible involvement of lipid peroxidation

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Cited by 16 publications
(9 citation statements)
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“…Severer oxidative damage was also found in the aortic media of older people (162). In human retinal vessels, aging induces the partial degeneration and loss of VSMCs and exacerbates oxidative stress (169,203). In rodent studies, the aortic tissues from aged mice exhibit mitochondrial dysfunction, and both cellular and mitochondrial levels of ROS are elevated in aortic tissues and VSMCs from aged mice (237,243).…”
Section: Other Factors Associated With Vascular Diseasementioning
confidence: 99%
“…Severer oxidative damage was also found in the aortic media of older people (162). In human retinal vessels, aging induces the partial degeneration and loss of VSMCs and exacerbates oxidative stress (169,203). In rodent studies, the aortic tissues from aged mice exhibit mitochondrial dysfunction, and both cellular and mitochondrial levels of ROS are elevated in aortic tissues and VSMCs from aged mice (237,243).…”
Section: Other Factors Associated With Vascular Diseasementioning
confidence: 99%
“…The aging process of the human retina often triggers oxidative stress reactions, inducing significant alterations within the retina [91]. Nag et al investigated changes in retinal blood vessels across various age groups using light and transmission electron microscopy, TUNEL, and immunohistochemistry [92]. The analysis encompassed vascular smooth muscle cells, oxidative stress, microglia, and blood vessels to evaluate the extent of human retinal aging.…”
Section: Retinal Vascular Aging: Pathophysiologymentioning
confidence: 99%
“…Lysosomes become incapable of completely breaking down all oxidized products of photoreceptor metabolism. This leads to the ferritin-mediated formation and accumulation of iron and non-degradable LF pigment in RPE lysosomes [39,66]. At the same time, LF can occupy The excessive accumulation of advanced glycation end products enhances the sensitivity of the RPE to pro-inflammatory stimuli, activates the transcription factor NF-κB, and leads to pathological ECM remodeling [82].…”
Section: Functional Prerequisite Of Rpe Cells For Oxidative Stressmentioning
confidence: 99%
“…Lysosomes become incapable of completely breaking down all oxidized products of photoreceptor metabolism. This leads to the ferritin-mediated formation and accumulation of iron and non-degradable LF pigment in RPE lysosomes [ 39 , 66 ]. At the same time, LF can occupy up to 25% of the volume of RPE cells, causing residual molecular components to accumulate in the cytoplasm and impairing their export through the plasma membrane [ 67 ].…”
Section: Functional Prerequisite Of Rpe Cells For Oxidative Stressmentioning
confidence: 99%