<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang S</submitter><funding>the Scientific and Technological Development Planning Foundation of Jilin Province</funding><funding>the Scientific and Technological Developing Scheme of Jilin Province</funding><funding>the Young Scientists Fund of the National Natural Science Foundation of China</funding><funding>the National Natural Science Foundation of China</funding><pagination>296</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9952469</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(2)</volume><pubmed_abstract>Ginsenosides, active substances in &lt;i>Panax ginseng&lt;/i> C. A. Meyer (ginseng), extend lifespan in multiple species, ameliorate age-associated damage, and limit functional decline in multiple tissues. However, their active components and their molecular mechanisms are largely unknown. Here, ginsenoside Rg1 (Rg1) promoted longevity in &lt;i>Saccharomyces cerevisiae&lt;/i>. Treatment with Rg1 decreased aging-mediated surface wrinkling, enhanced stress resistance, decreased reactive oxygen species' production and apoptosis, improved antioxidant enzyme activity, and decreased the aging rate. Proteomic analysis indicated that Rg1 delays &lt;i>S. cerevisiae&lt;/i> senescence by regulating metabolic homeostasis. Protein-protein interaction networks based on differential protein expression indicated that CDC19</pubmed_abstract><journal>Antioxidants (Basel, Switzerland)</journal><pubmed_title>Ginsenoside Rg1 Delays Chronological Aging in a Yeast Model via CDC19- and SDH2-Mediated Cellular Metabolism.</pubmed_title><pmcid>PMC9952469</pmcid><funding_grant_id>U19A2013</funding_grant_id><funding_grant_id>YDZJ202201ZYTS683</funding_grant_id><funding_grant_id>20210204188YY</funding_grant_id><funding_grant_id>82004074</funding_grant_id><pubmed_authors>Pan D</pubmed_authors><pubmed_authors>Yu S</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Liu M</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Jiang C</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Zhao D</pubmed_authors><pubmed_authors>Qiao J</pubmed_authors><pubmed_authors>Zhang P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ginsenoside Rg1 Delays Chronological Aging in a Yeast Model via CDC19- and SDH2-Mediated Cellular Metabolism.</name><description>Ginsenosides, active substances in &lt;i>Panax ginseng&lt;/i> C. A. Meyer (ginseng), extend lifespan in multiple species, ameliorate age-associated damage, and limit functional decline in multiple tissues. However, their active components and their molecular mechanisms are largely unknown. Here, ginsenoside Rg1 (Rg1) promoted longevity in &lt;i>Saccharomyces cerevisiae&lt;/i>. Treatment with Rg1 decreased aging-mediated surface wrinkling, enhanced stress resistance, decreased reactive oxygen species' production and apoptosis, improved antioxidant enzyme activity, and decreased the aging rate. Proteomic analysis indicated that Rg1 delays &lt;i>S. cerevisiae&lt;/i> senescence by regulating metabolic homeostasis. Protein-protein interaction networks based on differential protein expression indicated that CDC19</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-05T13:20:53.278Z</modification><creation>2025-02-18T23:58:01.567Z</creation></dates><accession>S-EPMC9952469</accession><cross_references><pubmed>36829855</pubmed><doi>10.3390/antiox12020296</doi></cross_references></HashMap>