Molecular mechanisms of diabetic retinopathy: potential therapeutic targets

Middle East Afr J Ophthalmol. 2015 Apr-Jun;22(2):135-44. doi: 10.4103/0974-9233.154386.

Abstract

Diabetic retinopathy (DR) is the leading cause of blindness in working-age adults in United States. Research indicates an association between oxidative stress and the development of diabetes complications. However, clinical trials with general antioxidants have failed to prove effective in diabetic patients. Mounting evidence from experimental studies that continue to elucidate the damaging effects of oxidative stress and inflammation in both vascular and neural retina suggest its critical role in the pathogenesis of DR. This review will outline the current management of DR as well as present potential experimental therapeutic interventions, focusing on molecules that link oxidative stress to inflammation to provide potential therapeutic targets for treatment or prevention of DR. Understanding the biochemical changes and the molecular events under diabetic conditions could provide new effective therapeutic tools to combat the disease.

Keywords: Diabetic Retinopathy; Endoplasmic Reticulum-stress; Inflammation; Nicotinamide Adenine Dinucleotide Phosphate Oxidase; Oxidative Stress; Peroxynitrite; Therapeutics.

Publication types

  • Review

MeSH terms

  • Angiogenesis Inhibitors / therapeutic use
  • Diabetes Complications
  • Diabetic Retinopathy / drug therapy*
  • Diabetic Retinopathy / etiology*
  • Diabetic Retinopathy / metabolism
  • Humans
  • NADPH Oxidases / adverse effects
  • NADPH Oxidases / metabolism
  • Oxidative Stress
  • Peroxynitrous Acid / adverse effects
  • Peroxynitrous Acid / metabolism
  • United States

Substances

  • Angiogenesis Inhibitors
  • Peroxynitrous Acid
  • NADPH Oxidases