March 2012
Volume 53, Issue 14
Free
ARVO Annual Meeting Abstract  |   March 2012
Neuroprotective Effect of Resveratrol after Optic Nerve Transection
Author Affiliations & Notes
  • SeokHwan Kim
    Ophthalmology, Boramae Hospital, Seoul, Republic of Korea
  • Joo Hyun Park
    Ophthalmology, Seoul National University Hospital, Seoul, Republic of Korea
  • Mi Jeung Kim
    Ophthalmology, Seoul National University Hospital, Seoul, Republic of Korea
  • Mi Jin Kim
    Ophthalmology, Seoul National University Bundang Hospital, Kyung-gi, Republic of Korea
  • Dong Myung Kim
    Ophthalmology, Seoul National University Hospital, Seoul, Republic of Korea
  • Jin Wook Jeoung
    Ophthalmology, Seoul National University Hospital, Seoul, Republic of Korea
  • Tae-Woo Kim
    Ophthalmology, Seoul National University Bundang Hospital, Seongnam, Republic of Korea
  • Ki Ho Park
    Ophthalmology, Seoul National University Hospital, Seoul, Republic of Korea
  • Footnotes
    Commercial Relationships  SeokHwan Kim, None; Joo Hyun Park, None; Mi Jeung Kim, None; Mi Jin Kim, None; Dong Myung Kim, None; Jin Wook Jeoung, None; Tae-Woo Kim, None; Ki Ho Park, None
  • Footnotes
    Support  This study was supported by a grant of the Korea Healthcare technology R & D Project, Ministry of Health & Welfare, Republic of Korea (A100228).
Investigative Ophthalmology & Visual Science March 2012, Vol.53, 6579. doi:
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      SeokHwan Kim, Joo Hyun Park, Mi Jeung Kim, Mi Jin Kim, Dong Myung Kim, Jin Wook Jeoung, Tae-Woo Kim, Ki Ho Park; Neuroprotective Effect of Resveratrol after Optic Nerve Transection. Invest. Ophthalmol. Vis. Sci. 2012;53(14):6579.

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

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Abstract

Purpose: : To investigate the neuroprotective effect of Resveratrol in an optic nerve transection model and to identify the neuroprotective mechanism of Resveratrol on retinal ganglion cells (RGC).

Methods: : Optic nerve transection and retrograde labeling were performed in SD rats. Various concentrations of Resveratrol (1ng/ul, 3ng/ul, 10ng/ul, 30ng/ul, 100ng/ul) were injected intravitreally immediately after optic nerve transection. The number of labeled RGCs was determined at 1 week and 2 weeks after optic nerve transection. The effect of Resveratrol and Sirtinol (SIRT1 inhibitor) co-injection was also investigated. RGC-5 cells were cultured and differentiated with staurosporin. MTT assay was performed to evaluate the effect of Resveratrol on RGC-5 cells in serum free condition. RGC-5 cells were cultured with Sirtinol to investigate the neuroprotective mechanism of Resveratrol.

Results: : A single intravitreal injection of Resveratrol (30ug/ul, 100ng/ul) was neuroprotective on RGC at 1 week after optic nerve transection (p<0.01). Dose-response relationship was observed between the concentration of Resveratrol and the neuroprotective effect. Repeated intravitreal injection of Resveratrol showed neuroprotective effect at 2 weeks after optic nerve transection (p<0.05). Co-injection of Resveratrol and Sirtinol diminished the neuroprotective effect of Resveratrol (p<0.01). Neuroprotective effect of Resveratrol was observed on RGC-5 cells in serum free condition and Sirtinol diminished the neuroprotective effect.

Conclusions: : Resveratrol exerts its neuroprotective effect via activation of the SIRT1 pathway in an optic nerve damage model. This finding demonstrates the therapeutic potential of Resveratrol in treating optic nerve diseases.

Keywords: neuroprotection • optic nerve • ganglion cells 
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