{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["9"],"submitter":["Zhou B"],"funding":["Capital Health Research and Development of Special Fund","Beijing Municipal Administration of Hospitals Clinical Medicine Development of Special Funding Support"],"pubmed_abstract":["Protein posttranslational modifications play important roles in cardiovascular diseases. The authors' previous report showed that the abundance of succinylated and glutarylated proteins was significantly lower in the serum of patients with acute myocardial infarction (AMI) than in that of healthy volunteers, suggesting a potential relationship between protein acylation and AMI. Sirtuin 5 (SIRT5) facilitates the removal of malonyl, succinyl, and glutaryl modification; however, its effects on AMI remain unknown. In this study, the levels of SIRT5 in AMI mouse model was compared. Results showed elevated hepatic SIRT5 after myocardial infarction. Hepatocyte-specific SIRT5 overexpressing mice (liver SIRT5 OE) were generated to address the possible involvement of hepatic SIRT5 in AMI. The areas "],"journal":["Frontiers in cell and developmental biology"],"pagination":["687559"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8339556"],"repository":["biostudies-literature"],"pubmed_title":["Cardioprotective Role of SIRT5 in Response to Acute Ischemia Through a Novel Liver-Cardiac Crosstalk Mechanism."],"pmcid":["PMC8339556"],"pubmed_authors":["Li W","Xiao M","Wei T","Zhou B","Hu H","Pei X","Du Y","Miao G","Wang J","Xue Y","Zhang P"],"additional_accession":[]},"is_claimable":false,"name":"Cardioprotective Role of SIRT5 in Response to Acute Ischemia Through a Novel Liver-Cardiac Crosstalk Mechanism.","description":"Protein posttranslational modifications play important roles in cardiovascular diseases. The authors' previous report showed that the abundance of succinylated and glutarylated proteins was significantly lower in the serum of patients with acute myocardial infarction (AMI) than in that of healthy volunteers, suggesting a potential relationship between protein acylation and AMI. Sirtuin 5 (SIRT5) facilitates the removal of malonyl, succinyl, and glutaryl modification; however, its effects on AMI remain unknown. In this study, the levels of SIRT5 in AMI mouse model was compared. Results showed elevated hepatic SIRT5 after myocardial infarction. Hepatocyte-specific SIRT5 overexpressing mice (liver SIRT5 OE) were generated to address the possible involvement of hepatic SIRT5 in AMI. The areas ","dates":{"release":"2021-01-01T00:00:00Z","publication":"2021","modification":"2025-04-19T00:32:06.417Z","creation":"2022-02-11T05:11:18.755Z"},"accession":"S-EPMC8339556","cross_references":{"pubmed":["34368135"],"doi":["10.3389/fcell.2021.687559"]}}