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  6. Keywords
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We are analyzing https://link.springer.com/article/10.1007/s11154-008-9090-4.

Title:
Oxidative stress and diabetic retinopathy: Pathophysiological mechanisms and treatment perspectives | Reviews in Endocrine and Metabolic Disorders
Description:
Retinopathy is one of the most severe ocular complications of diabetes and is a leading cause of acquired blindness in young adults. The cellular components of the retina are highly coordinated but very susceptible to the hyperglycemic environment. The microvasculature of the retina responds to hyperglycemic milieu through a number of biochemical changes, including increased oxidative stress and polyol pathway, PKC activation and advanced glycation end product formation. Oxidative stress is considered as one of the crucial contributors in the pathogenesis of diabetic retinopathy, but oxidative stress appears to be highly interrelated with other biochemical imbalances that lead to structural and functional changes and accelerated loss of capillary cells in the retinal microvasculature and, ultimately, pathological evidence of the disease. One such potential connection that links oxidative stress to metabolic alterations is gyceraldehyde-3-phosphate dehydrogenase whose activity is impaired in diabetes, and that results in activation of other major pathways implicated in the pathogenesis of diabetic retinopathy. Alterations associated with oxidative stress offer many potential therapeutic targets making this an area of great interest to the development of safe and effective treatments for diabetic retinopathy. Animal models of diabetic retinopathy have shown beneficial effects of antioxidants on the development of retinopathy, but clinical trials (though very limited in numbers) have provided somewhat ambiguous results. Although antioxidants are being used for other chronic diseases, controlled clinical trials are warranted to investigate potential beneficial effects of antioxidants in the development of retinopathy in diabetic patients.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Health & Fitness
  • Education
  • Science

Content Management System {πŸ“}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {πŸ“ˆ}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {πŸ’Έ}

We find it hard to spot revenue streams.

Earning money isn't the goal of every website; some are designed to offer support or promote social causes. People have different reasons for creating websites. This might be one such reason. Link.springer.com could be secretly minting cash, but we can't detect the process.

Keywords {πŸ”}

google, scholar, pubmed, article, cas, diabetes, diabetic, retinopathy, retinal, kowluru, stress, oxidative, res, role, dois, kern, doidiabetes, ophthalmol, retina, cell, complications, cells, development, biol, invest, sci, effect, med, protein, rats, activation, doi, apoptosis, glycation, experimental, free, advanced, radic, nuclear, vis, physiol, death, vascular, dehydrogenase, antioxidants, kinase, pathogenesis, eye, human, factor,

Topics {βœ’οΈ}

redox-active alpha-lipoic acid month download article/chapter age-related macular degeneration reactive oxygen species platelet-derived growth factor human d-glyceraldehyde-3-phosphate dehydrogenase intensive blood-glucose control advanced glycation end-products glucosamine-induced proliferation decrease endothelium-derived relaxing factor reversible post-translational modification nuclear factor-kappab induced alpha-tocopherol deficiency contrasted antioxid redox signal high glucose-induced apoptosis alpha lipoic acid alpha-lipoic acid complications research group human jurkat t-cells insulin-dependent diabetes mellitus diabetes-induced nitrative stress pkc beta isoenzyme mammalian glyceraldehyde-3-phosphate dehydrogenase vegf gene expression full article pdf stz-induced diabetic rats diabetes-induced retinal abnormalities diabetes-induced oxidative stress article madsen-bouterse glucose-induced apoptosis oral agent selective nuclear factor-kappab diabetes-induced mitochondrial dysfunction kowluru ra aldose reductase inhibitors privacy choices/manage cookies fluoride-induced apoptosis etoposide-induced apoptosis stitt aw nuclear transcriptional factor pre-apoptotic pericytes aldose reductase inhibitor fas mediated apoptosis serum ascorbic acid curr eye res frank rn kresge eye institute exp eye res free radic res wayne state university

Questions {❓}

  • What nitrates tyrosine?

Schema {πŸ—ΊοΈ}

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         description:Retinopathy is one of the most severe ocular complications of diabetes and is a leading cause of acquired blindness in young adults. The cellular components of the retina are highly coordinated but very susceptible to the hyperglycemic environment. The microvasculature of the retina responds to hyperglycemic milieu through a number of biochemical changes, including increased oxidative stress and polyol pathway, PKC activation and advanced glycation end product formation. Oxidative stress is considered as one of the crucial contributors in the pathogenesis of diabetic retinopathy, but oxidative stress appears to be highly interrelated with other biochemical imbalances that lead to structural and functional changes and accelerated loss of capillary cells in the retinal microvasculature and, ultimately, pathological evidence of the disease. One such potential connection that links oxidative stress to metabolic alterations is gyceraldehyde-3-phosphate dehydrogenase whose activity is impaired in diabetes, and that results in activation of other major pathways implicated in the pathogenesis of diabetic retinopathy. Alterations associated with oxidative stress offer many potential therapeutic targets making this an area of great interest to the development of safe and effective treatments for diabetic retinopathy. Animal models of diabetic retinopathy have shown beneficial effects of antioxidants on the development of retinopathy, but clinical trials (though very limited in numbers) have provided somewhat ambiguous results. Although antioxidants are being used for other chronic diseases, controlled clinical trials are warranted to investigate potential beneficial effects of antioxidants in the development of retinopathy in diabetic patients.
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      headline:Oxidative stress and diabetic retinopathy: Pathophysiological mechanisms and treatment perspectives
      description:Retinopathy is one of the most severe ocular complications of diabetes and is a leading cause of acquired blindness in young adults. The cellular components of the retina are highly coordinated but very susceptible to the hyperglycemic environment. The microvasculature of the retina responds to hyperglycemic milieu through a number of biochemical changes, including increased oxidative stress and polyol pathway, PKC activation and advanced glycation end product formation. Oxidative stress is considered as one of the crucial contributors in the pathogenesis of diabetic retinopathy, but oxidative stress appears to be highly interrelated with other biochemical imbalances that lead to structural and functional changes and accelerated loss of capillary cells in the retinal microvasculature and, ultimately, pathological evidence of the disease. One such potential connection that links oxidative stress to metabolic alterations is gyceraldehyde-3-phosphate dehydrogenase whose activity is impaired in diabetes, and that results in activation of other major pathways implicated in the pathogenesis of diabetic retinopathy. Alterations associated with oxidative stress offer many potential therapeutic targets making this an area of great interest to the development of safe and effective treatments for diabetic retinopathy. Animal models of diabetic retinopathy have shown beneficial effects of antioxidants on the development of retinopathy, but clinical trials (though very limited in numbers) have provided somewhat ambiguous results. Although antioxidants are being used for other chronic diseases, controlled clinical trials are warranted to investigate potential beneficial effects of antioxidants in the development of retinopathy in diabetic patients.
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External Links {πŸ”—}(500)

Analytics and Tracking {πŸ“Š}

  • Google Tag Manager

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  • Clipboard.js
  • Prism.js

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