Dopamine ameliorates hyperglycemic memory-induced microvascular dysfunction in diabetic retinopathy

FASEB J. 2022 Dec;36(12):e22643. doi: 10.1096/fj.202200865R.

Abstract

Dopamine is a neurotransmitter that mediates visual function in the retina and diabetic retinopathy (DR) is the most common microvascular complication of diabetes and the leading cause of blindness; however, the role of dopamine in retinal vascular dysfunction in DR remains unclear. Here, we report a mechanism of hyperglycemic memory (HGM)-induced retinal microvascular dysfunction and the protective effect of dopamine against the HGM-induced retinal microvascular leakage and abnormalities. We found that HGM induced persistent oxidative stress, mitochondrial membrane potential collapse and fission, and adherens junction disassembly and subsequent vascular leakage after blood glucose normalization in the mouse retinas. These persistent hyperglycemic stresses were inhibited by dopamine treatment in human retinal endothelial cells and by intravitreal injection of levodopa in the retinas of HGM mice. Moreover, levodopa supplementation ameliorated HGM-induced pericyte degeneration, acellular capillary and pericyte ghost generation, and endothelial apoptosis in the mouse retinas. Our findings suggest that dopamine alleviates HGM-induced retinal microvascular leakage and abnormalities by inhibiting persistent oxidative stress and mitochondrial dysfunction.

Keywords: diabetic retinopathy; dopamine; hyperglycemic memory; microvascular dysfunction; mitochondrial dysfunction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Diabetes Mellitus*
  • Diabetic Retinopathy* / drug therapy
  • Dopamine
  • Endothelial Cells
  • Humans
  • Levodopa / pharmacology
  • Mice
  • Retina
  • Retinal Vessels

Substances

  • Dopamine
  • Levodopa