<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Teertam SK</submitter><funding>Department of Biotechnology , Ministry of Science and Technology</funding><funding>Department of Science and Technology, Ministry of Science and Technology, India</funding><funding>Department of Science and Technology, Ministry of Science and Technology</funding><pagination>6339</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7973546</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(1)</volume><pubmed_abstract>Cerebral ischemia (CI) is a severe cause of neurological dysfunction and mortality. Sirtuin-1 (Silent information regulator family protein 1, SIRT1), an oxidized nicotinamide adenine dinucleotide (NAD&lt;sup>+&lt;/sup>)-dependent protein deacetylase, plays an important role in protection against several neurodegenerative disorders. The present study aims to investigate the protective role of SIRT1 after CI in experimental young and aged rats and humans. Also, the study examines the possible regulatory mechanisms of neuronal death in CI settings. Immunoblotting and immunohistochemistry were used to evaluate changes in the expression of SIRT1, JNK/ERK/MAPK/AKT signaling, and pro-apoptotic caspase-3 in experimental rats and CI patients. The study findings demonstrated that, in aged experimental rat</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Differential role of SIRT1/MAPK pathway during cerebral ischemia in rats and humans.</pubmed_title><pmcid>PMC7973546</pmcid><funding_grant_id>DBT/04/0401/2017/01181</funding_grant_id><funding_grant_id>CRG/2020/005021</funding_grant_id><funding_grant_id>SR/CSRI/196/2016</funding_grant_id><pubmed_authors>Teertam SK</pubmed_authors><pubmed_authors>Prakash Babu P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Differential role of SIRT1/MAPK pathway during cerebral ischemia in rats and humans.</name><description>Cerebral ischemia (CI) is a severe cause of neurological dysfunction and mortality. Sirtuin-1 (Silent information regulator family protein 1, SIRT1), an oxidized nicotinamide adenine dinucleotide (NAD&lt;sup>+&lt;/sup>)-dependent protein deacetylase, plays an important role in protection against several neurodegenerative disorders. The present study aims to investigate the protective role of SIRT1 after CI in experimental young and aged rats and humans. Also, the study examines the possible regulatory mechanisms of neuronal death in CI settings. Immunoblotting and immunohistochemistry were used to evaluate changes in the expression of SIRT1, JNK/ERK/MAPK/AKT signaling, and pro-apoptotic caspase-3 in experimental rats and CI patients. The study findings demonstrated that, in aged experimental rat</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-18T13:27:35.924Z</modification><creation>2025-04-06T23:13:20.686Z</creation></dates><accession>S-EPMC7973546</accession><cross_references><pubmed>33737560</pubmed><doi>10.1038/s41598-021-85577-9</doi></cross_references></HashMap>