March 2012
Volume 53, Issue 14
Free
ARVO Annual Meeting Abstract  |   March 2012
Effect Of Coenzyme Q10 On Mitochondrial Fission And Cellular ATP Reduction In Purified Rat Optic Nerve Head Astrocytes Exposed To Hydrogen Peroxide
Author Affiliations & Notes
  • You Hyun Noh
    Hamilton Glaucoma Center and Department of Ophthalmology, University of California, San Diego, La Jolla, California
  • Keun-Young Kim
    National Center for Microscopy and Imaging Research and Department of Neuroscience, University of California, San Diego School of Medicine, La Jolla, California
  • Robert N. Weinreb
    Hamilton Glaucoma Center and Department of Ophthalmology, University of California, San Diego, La Jolla, California
  • Won-Kyu Ju
    Hamilton Glaucoma Center and Department of Ophthalmology, University of California, San Diego, La Jolla, California
  • Footnotes
    Commercial Relationships  You Hyun Noh, None; Keun-Young Kim, None; Robert N. Weinreb, None; Won-Kyu Ju, None
  • Footnotes
    Support  NIH EY018658
Investigative Ophthalmology & Visual Science March 2012, Vol.53, 6617. doi:
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      You Hyun Noh, Keun-Young Kim, Robert N. Weinreb, Won-Kyu Ju; Effect Of Coenzyme Q10 On Mitochondrial Fission And Cellular ATP Reduction In Purified Rat Optic Nerve Head Astrocytes Exposed To Hydrogen Peroxide. Invest. Ophthalmol. Vis. Sci. 2012;53(14):6617.

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

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Abstract

Purpose: : To determine whether hydrogen peroxide-induced oxidative stress triggers mitochondrial fission and cellular ATP reduction, as well as whether coenzyme Q10 (CoQ10) blocks mitochondrial fission and restores cellular ATP production in primary rat optic nerve head (ONH) astrocytes.

Methods: : The purified ONH astrocytes from rat were cultured by pre-incubation with 50 μg/ml of CoQ10 for 24 hours and then exposed to hydrogen peroxide (100 μM) for 1 hour. Mitochondrial morphology was assessed by MitoTracker Red staining. The cellular viability was measured by MTT assay and cellular ATP production was assessed by a luciferase-based assay.

Results: : Hydrogen peroxide treatment triggered mitochondrial fission, characterized by the conversion of tubular fused mitochondria into isolated small organelles, as well as significantly decreased cell viability by 79.5 ± 4.4% and induced a significant reduction of cellular ATP level by 80 ± 9.8% in the ONH astrocytes compared with control cells (P < 0.05). In contrast, CoQ10 treatment blocks mitochondrial fission in hydrogen peroxide-treated ONH astrocytes. In addition, CoQ10 treatment significantly increased cell viability by 115.4 ± 5.2% and restored cellular ATP production by 102.7 ± 4.7% in hydrogen peroxide-treated ONH astrocytes (P < 0.05).

Conclusions: : These results provide the evidence that CoQ10 may be useful to protect ONH astrocytes against oxidative stress-mediated mitochondrial dysfunction. Based on this observation, we propose that oxidative stress-mediated mitochondrial dysfunction may be an important degenerative pathway in the ONH astrocytes during glaucomatous degeneration.

Keywords: astrocytes: optic nerve head • oxidation/oxidative or free radical damage • antioxidants 
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