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Neuroprotective Effect of Resveratrol via Sirtuin 1 Pathway in a Rat Model of Chronic Ocular Hypertension

Hwan Heo, Mi Sun Sung, Sang Woo Park

Journal of the Korean Glaucoma Society · 2018

Abstract

Several optic neuropathies, including glaucoma, lead to optic nerve axonal damage and retinal ganglion cell (RGC) loss via apoptosis.1 Glaucomatous optic neuropathy is characterized by progressive axonal damage in the optic nerve head, which progresses to RGC death and visual field deficits.2 Since recognition of the promising role for silent information regulators in the longevity of Caenorhabditis elegans, many studies have focused on the cellular mechanisms underlying sirtuins.3 Sirtuin 1 (SIRT1) is a nicotinamide adenine dinucleotide (NAD)+-dependent histone deacetylase, which is linked to cellular stress responses and survival functions including metabolic control, DNA repair, inflammation, apoptosis, and neuroprotection.4,5 Studies conducted to date indicate that SIRT1 contributes to neuroprotection during ischemia and in the neurodegenerative diseases.[6][7][8] SIRT1 overexpression by resveratrol pretreatment mediates delayed neuronal death following cerebral ischemic damage in rats.9 In contrast, inhibition of SIRT1 increases cortical

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OpenAlex
DOI
10.36299/jkgs.2018.7.1.1
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2026-11-01 MST

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APA
Heo, H., Sung, M.S., &amp; Park, S.W. (2018). Neuroprotective Effect of Resveratrol via Sirtuin 1 Pathway in a Rat Model of Chronic Ocular Hypertension. <em>Journal of the Korean Glaucoma Society</em>. https://doi.org/10.36299/jkgs.2018.7.1.1
Vancouver
Heo H, Sung MS, Park SW. Neuroprotective Effect of Resveratrol via Sirtuin 1 Pathway in a Rat Model of Chronic Ocular Hypertension. Journal of the Korean Glaucoma Society. 2018. doi:10.36299/jkgs.2018.7.1.1.
BibTeX
@article{hwan2018Neurop, title = {Neuroprotective Effect of Resveratrol via Sirtuin 1 Pathway in a Rat Model of Chronic Ocular Hypertension}, author = {Hwan Heo and Mi Sun Sung and Sang Woo Park}, journal = {Journal of the Korean Glaucoma Society}, year = {2018}, doi = {10.36299/jkgs.2018.7.1.1}, }

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