<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xiao H</submitter><funding>Guangdong Basic and Applied Basic Research Foundation</funding><pagination>2700000</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9001072</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2022</volume><pubmed_abstract>More and more attention has been paid to the use of traditional phytochemicals. Here, we first verified the therapeutic potential of a natural bioactive compound called Hinokitiol in myocardial ischemia reperfusion injury. Hinokitiol exerts cardioprotective effect through inhibition of GSK-3&lt;i>β&lt;/i> and subsequent elimination of excessive autophagy, tuning autophagic activity in moderate extent for remedial profit in acute myocardial infarction and myocardial ischemia reperfusion injury. Overall, our study establishes Hinokitiol as a novel available interventional treatment for myocardial ischemia reperfusion injury.</pubmed_abstract><journal>Oxidative medicine and cellular longevity</journal><pubmed_title>Hinokitiol Protects Cardiomyocyte from Oxidative Damage by Inhibiting GSK3&lt;i>β&lt;/i>-Mediated Autophagy.</pubmed_title><pmcid>PMC9001072</pmcid><funding_grant_id>2018A030313980</funding_grant_id><pubmed_authors>Liang S</pubmed_authors><pubmed_authors>Cai Q</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Yang Z</pubmed_authors><pubmed_authors>Xiao H</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Jin L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hinokitiol Protects Cardiomyocyte from Oxidative Damage by Inhibiting GSK3&lt;i>β&lt;/i>-Mediated Autophagy.</name><description>More and more attention has been paid to the use of traditional phytochemicals. Here, we first verified the therapeutic potential of a natural bioactive compound called Hinokitiol in myocardial ischemia reperfusion injury. Hinokitiol exerts cardioprotective effect through inhibition of GSK-3&lt;i>β&lt;/i> and subsequent elimination of excessive autophagy, tuning autophagic activity in moderate extent for remedial profit in acute myocardial infarction and myocardial ischemia reperfusion injury. Overall, our study establishes Hinokitiol as a novel available interventional treatment for myocardial ischemia reperfusion injury.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-20T00:17:16.023Z</modification><creation>2025-02-19T01:53:31.607Z</creation></dates><accession>S-EPMC9001072</accession><cross_references><pubmed>35419165</pubmed><doi>10.1155/2022/2700000</doi></cross_references></HashMap>