Investigative Ophthalmology & Visual Science Cover Image for Volume 65, Issue 7
June 2024
Volume 65, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2024
Effect of Co-enzyme Q10 eyedrops on neurodegeneration and mitochondrial dysfunction in the retina of a type 2 diabetic mice model
Author Affiliations & Notes
  • Hang I Christie Lam
    School of Optometry, The Hong Kong Polytechnic University, Hong Kong, Hong Kong
    Centre for Eye and Vision Research Limited, Hong Kong, Hong Kong
  • Dennis Yan-Yin Tse
    School of Optometry, The Hong Kong Polytechnic University, Hong Kong, Hong Kong
    Centre for Eye and Vision Research Limited, Hong Kong, Hong Kong
  • Footnotes
    Commercial Relationships   Hang I Christie Lam None; Dennis Tse None
  • Footnotes
    Support  HKPolyU RCSV Smaller scale project 1-BBCX; UGC project U-ZEZ2; InnoHK scheme from HKSAR Government
Investigative Ophthalmology & Visual Science June 2024, Vol.65, 301. doi:
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      Hang I Christie Lam, Dennis Yan-Yin Tse; Effect of Co-enzyme Q10 eyedrops on neurodegeneration and mitochondrial dysfunction in the retina of a type 2 diabetic mice model. Invest. Ophthalmol. Vis. Sci. 2024;65(7):301.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : Current treatments for diabetic retinopathy (DR), one of the leading causes of blindness and vision impairment, are invasive and possess several limitations. Developing new treatment regimens to arrest its development and progression to proliferative stage to preserve vision is imperative. Mitochondrial dysfunction has been implicated in the pathogenesis of DR. Here, we test the effect of Coenzyme Q10 (CoQ10) eyedrops, a proven antioxidant and mitochondrial stabilizer, on DR with a type 2 diabetic mouse model as to investigate the potential of CoQ10 eyedrops as a non-invasive treatment option for DR.

Methods : Male C57BL/KsJ-db/db (db/db) mice aged 9 weeks with fasting blood glucose levels ≥ 13.9 mmol/L were used. CoQ10 eyedrops conjugated with Vitamin E TPGS were instilled twice daily to the treatment group (CoQ10, n=7), and PBS was given to the control group (control, n=6). After 4 months of treatment, the retinas of the mice were harvested to assess the morphology and ex-vivo mitochondrial bioenergetics with immunohistochemistry and the Seahorse XFe24 analyzer, respectively.

Results : The db/db mice treated with CoQ10 eyedrops were found to have thicker outer (ONL) and inner nuclear layers (INL) compared to the control mice (ONL: control=53.6±2.0 μm vs. CoQ10=60.3±2.0 μm, p=0.038; INL: control=30.9±1.6 μm vs. CoQ10=39.0±0.6 μm, p=0.002). Their retinas were also found to have a higher photoreceptor (control=316.4±14.4 vs. CoQ10=380.8±18.0, p=0.019) and cone cell density (control=28.8±4.1 vs. CoQ10=43.8±2.1, p=0.006) than the control. The retina of CoQ10 treated db/db mice also exhibited stronger mitochondrial functions compared to the control (Basal respiration:1.37±0.14-fold, p=0.044; Maximal respiration: 1.59±0.15-fold, p=0.031; Spare capacity: 6.13±0.90-fold, p=0.003).

Conclusions : Our data indicates that CoQ10 eyedrops ameliorated retinal neurodegeneration and associated mitochondrial dysfunction in diabetic mice. It provides further insight on the role of mitochondrial dysfunction in the pathogenesis of diabetic retinopathy and suggests that CoQ10 eyedrops may be a potential therapeutic option for DR-related neuropathy.

This abstract was presented at the 2024 ARVO Annual Meeting, held in Seattle, WA, May 5-9, 2024.

 

Fig1. Representative confocal images and bar charts comparing the thicknesses of (a-c) the outer nuclear layer (ONL) and inner nuclear layer (INL); (d-f) photoreceptor and cone cell density of the control and CoQ10-treated db/db mice.

Fig1. Representative confocal images and bar charts comparing the thicknesses of (a-c) the outer nuclear layer (ONL) and inner nuclear layer (INL); (d-f) photoreceptor and cone cell density of the control and CoQ10-treated db/db mice.

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