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Experimental Drug Targets Hypoglycemia-Induced Retinal Damage in Diabetic Retinopathy

Researchers identify HIF protein as a key driver of blood-retinal barrier breakdown in diabetic mice and propose clinical trials for HIF inhibitor 32-134D.

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Now, scientists have found that HIF is a player in how the blood-retinal barrier breaks down during hypoglycemia. Credit: Neuroscience News
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Overview

  • A new NIH-funded study reveals that hypoglycemia disrupts the blood-retinal barrier in diabetic mice, leading to retinal vessel leakage and vision loss.
  • The study identifies hypoxia-inducible factors (HIF-1α and HIF-2α) as critical proteins accumulating during low blood sugar episodes, triggering retinal damage.
  • The experimental drug 32-134D successfully inhibits HIF activity in diabetic mice, preventing blood-retinal barrier breakdown and vascular leakage.
  • Findings explain why tight glycemic control or high glucose variability can paradoxically worsen diabetic eye disease through hypoglycemia-driven pathways.
  • Researchers are now planning early-phase clinical trials to evaluate the safety and efficacy of 32-134D in patients with diabetic retinopathy.