PXD057532 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Comparative analysis of metabolic and functional cardiac alterations in diet- and genetically induced mouse models of heart failure |
| Description | This study aimed to elucidate the metabolic and functional alterations in heart failure in two mouse models with different heart failure phenotypes. C57BL/6J mice fed a high-fat diet (Black6 HF) and New Zealand Obese mice fed a standard diet (NZO SD) were analyzed compared to Black6 SD controls. Functional parameters of the heart were assessed through echocardiography. Additionally, plasma metabolites and tissue fibrosis were analyzed. Proteomics data from heart tissue were incorporated into a detailed kinetic model of central cardiac metabolism (CARDIOKIN1) to evaluate metabolic capacities. We demonstrate distinct structural and functional cardiac impairments, nutritional imbalances, and metabolic adaptations. Black6 HF mice exhibited cardiac dysfunction with normal ejection fraction, and decreased cardiac mass and inflammation, but without fibrosis while maintaining stable plasma nutrient composition. In contrast, NZO SD mice displayed heart failure with reduced ejection fraction, increased heart mass, significant derangement of circulating plasma nutrients, and mild fibrosis, but no inflammation. Proteomic analysis and kinetic modeling revealed that mitochondrial dysfunction and reduced ATP production capacity are key drivers of heart failure in Black6 HF mice, while NZO SD mice maintained ATP production capacity but showed significant alterations in substrate utilization capacities under variable energy demands. Our findings highlight the critical role of metabolic adaptation in heart failure emphasizing the importance of metabolic flexibility and efficiency. This study underscores the complex interplay between metabolic, structural, and functional changes in heart failure, providing valuable insights into and underpinning the different basis for treatment strategies for different forms of this syndrome. |
| HostingRepository | PRIDE |
| AnnounceDate | 2026-04-27 |
| AnnouncementXML | Submission_2026-04-26_21:25:59.581.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Christoph Gille |
| SpeciesList | scientific name: Mus musculus (Mouse); NCBI TaxID: NEWT:10090; |
| ModificationList | No PTMs are included in the dataset |
| Instrument | Q Exactive |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2024-11-05 05:34:32 | ID requested | |
| ⏵ 1 | 2026-04-26 21:26:00 | announced | |
Publication List
| 10.1111/febs.70362; |
| Ott C, Baumgarten P, Henning T, Weber D, Wallach I, Grune J, Kintscher U, Holzh, ü, tter HG, Grune T, Berndt N, Comparative analysis of metabolic and functional cardiac alterations in diet- and genetically induced mouse models of cardiac dysfunction. FEBS J, 293(8):2454-2477(2026) [pubmed] |
Keyword List
| submitter keyword: High-fat diet, cardiac metabolism, genetically induced obesity, heart failure, metabolic adaptation, cardiac function |
Contact List
| Nicolaus Berndt |
| contact affiliation | Deutsches Herzzentrum der Charité (DHZC), Institute of Computer-assisted Cardiovascular Medicine |
| contact email | nikolaus.berndt@dhzc-charite.de |
| lab head | |
| Christoph Gille |
| contact affiliation | Core Facility -High-Throughput Mass Spectrometry, Charité |
| contact email | christoph.gille@charite.de |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
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| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD057532
- Label: PRIDE project
- Name: Comparative analysis of metabolic and functional cardiac alterations in diet- and genetically induced mouse models of heart failure