<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2022</volume><submitter>Zeng Y</submitter><pubmed_abstract>Subarachnoid hemorrhage (SAH) as a devastating neurological disorder is closely related to heightened oxidative insults and neuroinflammatory injury. Pinocembrin, a bioflavonoid, exhibits different biological functions, such as immunomodulatory, anti-inflammatory, antioxidative, and cerebroprotective activities. Herein, we examined the protective effects and molecular mechanisms of pinocembrin in a murine model of SAH. Using an endovascular perforation model in rats, pinocembrin significantly mitigated SAH-induced neuronal tissue damage, including inflammatory injury and free-radical insults. Meanwhile, pinocembrin improved behavior function and reduced neuronal apoptosis. We also revealed that sirtuin-1 (SIRT1) activation was significantly enhanced by pinocembrin. In addition, pinocembrin</pubmed_abstract><journal>Oxidative medicine and cellular longevity</journal><pagination>2242833</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9683949</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Activation of Sirtuin-1 by Pinocembrin Treatment Contributes to Reduced Early Brain Injury after Subarachnoid Hemorrhage.</pubmed_title><pmcid>PMC9683949</pmcid><pubmed_authors>Wu Z</pubmed_authors><pubmed_authors>Lai J</pubmed_authors><pubmed_authors>Fang Z</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Hu W</pubmed_authors><pubmed_authors>Guo X</pubmed_authors><pubmed_authors>Lin W</pubmed_authors><pubmed_authors>Zeng Y</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Yao H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Activation of Sirtuin-1 by Pinocembrin Treatment Contributes to Reduced Early Brain Injury after Subarachnoid Hemorrhage.</name><description>Subarachnoid hemorrhage (SAH) as a devastating neurological disorder is closely related to heightened oxidative insults and neuroinflammatory injury. Pinocembrin, a bioflavonoid, exhibits different biological functions, such as immunomodulatory, anti-inflammatory, antioxidative, and cerebroprotective activities. Herein, we examined the protective effects and molecular mechanisms of pinocembrin in a murine model of SAH. Using an endovascular perforation model in rats, pinocembrin significantly mitigated SAH-induced neuronal tissue damage, including inflammatory injury and free-radical insults. Meanwhile, pinocembrin improved behavior function and reduced neuronal apoptosis. We also revealed that sirtuin-1 (SIRT1) activation was significantly enhanced by pinocembrin. In addition, pinocembrin</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T19:51:19.903Z</modification><creation>2025-04-04T19:51:19.903Z</creation></dates><accession>S-EPMC9683949</accession><cross_references><pubmed>36439686</pubmed><doi>10.1155/2022/2242833</doi></cross_references></HashMap>