<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>64(7)</volume><submitter>Xiao K</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>The purpose of this study was to investigate the protective effect of low-dose trans-resveratrol (trans-RSV) on diabetes-induced retinal ganglion cell (RGC) degeneration and its possible mechanism.&lt;h4>Methods&lt;/h4>A streptozotocin-induced diabetic mouse model was established and treated with or without trans-RSV intragastric administration (10 mg/kg body weight/day) for 12 weeks. Oscillatory potentials (Ops) of the dark-adapted electroretinogram (ERG) were recorded. The number of RGCs was detected by Tuj1 and TUNEL staining. The apoptosis markers in the retina were analyzed by Western blot. The cross sections of optic nerves were observed by transmission electron microscopy. In addition, mouse neuroblastoma N2a cells were injured by high-glucose (HG) treatment. Cell viabilit</pubmed_abstract><journal>Investigative ophthalmology &amp; visual science</journal><pagination>2</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10241309</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Low-Dose Trans-Resveratrol Ameliorates Diabetes-Induced Retinal Ganglion Cell Degeneration via TyrRS/c-Jun Pathway.</pubmed_title><pmcid>PMC10241309</pmcid><pubmed_authors>Xiao K</pubmed_authors><pubmed_authors>Ma XH</pubmed_authors><pubmed_authors>Sun XF</pubmed_authors><pubmed_authors>Chen XH</pubmed_authors><pubmed_authors>Zhong Z</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Low-Dose Trans-Resveratrol Ameliorates Diabetes-Induced Retinal Ganglion Cell Degeneration via TyrRS/c-Jun Pathway.</name><description>&lt;h4>Purpose&lt;/h4>The purpose of this study was to investigate the protective effect of low-dose trans-resveratrol (trans-RSV) on diabetes-induced retinal ganglion cell (RGC) degeneration and its possible mechanism.&lt;h4>Methods&lt;/h4>A streptozotocin-induced diabetic mouse model was established and treated with or without trans-RSV intragastric administration (10 mg/kg body weight/day) for 12 weeks. Oscillatory potentials (Ops) of the dark-adapted electroretinogram (ERG) were recorded. The number of RGCs was detected by Tuj1 and TUNEL staining. The apoptosis markers in the retina were analyzed by Western blot. The cross sections of optic nerves were observed by transmission electron microscopy. In addition, mouse neuroblastoma N2a cells were injured by high-glucose (HG) treatment. Cell viabilit</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jun</publication><modification>2025-04-04T14:40:02.506Z</modification><creation>2025-04-04T14:40:02.506Z</creation></dates><accession>S-EPMC10241309</accession><cross_references><pubmed>37261387</pubmed><doi>10.1167/iovs.64.7.2</doi></cross_references></HashMap>