Coenzyme Q10 and Fish Oil Supplementation for Reducing Retinal Oxidative Stress in a Rat Model

Faisal Siddiqui1, Charles Cai2, Jacob V Aranda1,2,3

  • 1Department of Pediatrics, Division of Neonatal-Perinatal Medicine, State University of New York, Downstate Health Sciences University, Brooklyn, NY 11203, USA.

Insights

Early Coenzyme Q10 (CoQ10) supplementation significantly reduced retinopathy of prematurity in rat pups exposed to intermittent hypoxia (IH). CoQ10 offered superior protection against IH-induced oxidative stress and retinopathy compared to fish oil.

Area of Science:

  • Neonatal Medicine
  • Ophthalmology
  • Biochemistry

Background:

  • Premature neonates requiring oxygen therapy often experience intermittent hypoxia (IH).
  • IH episodes increase the risk of oxidative stress and retinopathy of prematurity (ROP).
  • Early nutritional interventions are explored to mitigate IH-induced damage.

Purpose of the Study:

  • To investigate the protective effects of early fish oil or coenzyme Q10 (CoQ10) supplementation against IH-induced retinopathy.
  • To compare the efficacy of CoQ10 versus fish oil in reducing IH-related ocular damage.

Main Methods:

  • Rat pups were exposed to two neonatal IH paradigms with recovery periods.
  • Intervention groups received daily oral fish oil, CoQ10, or olive oil (vehicle) for 14 days.
  • Retinal examinations were performed at postnatal days 14 and 21 to assess retinopathy and oxidative stress.

Main Results:

  • Both IH paradigms induced severe retinopathy and oxidative stress in vehicle-treated pups.
  • Early fish oil supplementation showed some benefits.
  • CoQ10 supplementation provided superior protection, significantly reducing IH-induced oxidative stress and retinopathy, with lower retinal antioxidants and angiogenesis biomarkers.

Conclusions:

  • Coenzyme Q10 (CoQ10) demonstrates significant therapeutic potential for preventing and treating retinopathy of prematurity caused by intermittent hypoxia (IH).
  • CoQ10's protective effects involve reducing oxidative stress and modulating angiogenesis.
  • Further research is necessary to determine optimal and safe dosages for preterm infants.

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