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1000 Titel
  • Oxidative stress initiates hemodynamic change in CKD-induced heart disease
1000 Autor/in
  1. Sen, Payel |
  2. Hamers, Jules |
  3. Sittig, Theresa |
  4. Shashikadze, Bachuki |
  5. d’Ambrosio, Laura |
  6. Stöckl, Jan B. |
  7. Bierschenk, Susanne |
  8. Zhang, Hengliang |
  9. d’Alessio, Chiara |
  10. Zandbergen, Lotte Maria |
  11. Pauly, Valerie |
  12. Clauss, Sebastian |
  13. Wolf, Eckhard |
  14. Dendorfer, Andreas |
  15. Fröhlich, Thomas |
  16. Merkus, Daphne |
1000 Verlag Springer Berlin Heidelberg
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-10-15
1000 Erschienen in
1000 Quellenangabe
  • 119(6):957-971
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00395-024-01085-7 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11628585/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:p>Chronic kidney disease (CKD) predisposes to cardiac remodeling and coronary microvascular dysfunction. Studies in swine identified changes in microvascular structure and function, as well as changes in mitochondrial structure and oxidative stress. However, CKD was combined with metabolic derangement, thereby obscuring the contribution of CKD alone. Therefore, we studied the impact of CKD on the heart and combined proteome studies with measurement of cardiac function and perfusion to identify processes involved in cardiac remodeling in CKD. CKD was induced in swine at 10–12 weeks of age while sham-operated swine served as controls. 5–6 months later, left ventricular (LV) function and coronary flow reserve were measured. LC–MS–MS-based proteomic analysis of LV tissue was performed. LV myocardium and kidneys were histologically examined for interstitial fibrosis and oxidative stress. Renal embolization resulted in mild chronic kidney injury (increased fibrosis and urinary NGAL). PV loops showed LV dilation and increased wall stress, while preload recruitable stroke work was impaired in CKD. Quantitative proteomic analysis of LV myocardium and STRING pre-ranked functional analysis showed enrichments in pathways related to contractile function, reactive oxygen species, and extracellular matrix (ECM) remodeling, which were confirmed histologically and associated with impaired total anti-oxidant capacity. H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> exposure of myocardial slices from CKD, but not normal swine, impaired contractile function. Furthermore, in CKD, mitochondrial proteins were downregulated suggesting mitochondrial dysfunction which was associated with higher basal coronary blood flow. Thus, mild CKD induces alterations in mitochondrial proteins along with contractile proteins, oxidative stress and ECM remodeling, that were associated with changes in cardiac function and perfusion.</jats:p>
1000 Sacherschließung
lokal Renal Insufficiency, Chronic/physiopathology [MeSH]
lokal Ventricular Function, Left [MeSH]
lokal Cardiac remodeling
lokal Proteomics [MeSH]
lokal Original Contribution
lokal Oxidative Stress [MeSH]
lokal Proteomics
lokal Chronic kidney disease
lokal Coronary flow reserve
lokal Disease Models, Animal [MeSH]
lokal Myocardium/metabolism [MeSH]
lokal Swine [MeSH]
lokal Fibrosis [MeSH]
lokal Renal Insufficiency, Chronic/metabolism [MeSH]
lokal Animals [MeSH]
lokal Heart Diseases/etiology [MeSH]
lokal Renal Insufficiency, Chronic/pathology [MeSH]
lokal Myocardium/pathology [MeSH]
lokal Heart Diseases/physiopathology [MeSH]
lokal Oxidative stress
lokal Coronary Circulation [MeSH]
lokal Heart Diseases/metabolism [MeSH]
lokal Hemodynamics [MeSH]
lokal Heart Diseases/pathology [MeSH]
lokal Ventricular Remodeling [MeSH]
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-1613-7760|https://orcid.org/0000-0002-9715-2005|https://frl.publisso.de/adhoc/uri/U2l0dGlnLCBUaGVyZXNh|https://orcid.org/0000-0003-4558-0785|https://frl.publisso.de/adhoc/uri/ZOKAmUFtYnJvc2lvLCBMYXVyYQ==|https://frl.publisso.de/adhoc/uri/U3TDtmNrbCwgSmFuIEIu|https://frl.publisso.de/adhoc/uri/QmllcnNjaGVuaywgU3VzYW5uZQ==|https://orcid.org/0000-0002-8174-7215|https://frl.publisso.de/adhoc/uri/ZOKAmUFsZXNzaW8sIENoaWFyYQ==|https://orcid.org/0000-0001-6156-8095|https://frl.publisso.de/adhoc/uri/UGF1bHksIFZhbGVyaWU=|https://orcid.org/0000-0002-5675-6128|https://orcid.org/0000-0002-0430-9510|https://orcid.org/0000-0002-7806-312X|https://orcid.org/0000-0002-4709-3211|https://orcid.org/0000-0002-4852-831X
1000 Hinweis
  • DeepGreen-ID: ecffb5357123400385f8c5d393b71720 ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
1000 Label
1000 Förderer
  1. Deutsches Zentrum für Herz-Kreislaufforschung |
  2. Friedrich Bauer Foundation |
  3. Chinese Government Scholarship |
  4. Dutch Cardiovascular Alliance |
  5. Klinikum der Universität München |
1000 Fördernummer
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1000 Förderprogramm
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1000 Dateien
  1. Oxidative stress initiates hemodynamic change in CKD-induced heart disease
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer Deutsches Zentrum für Herz-Kreislaufforschung |
    1000 Förderprogramm -
    1000 Fördernummer -
  2. 1000 joinedFunding-child
    1000 Förderer Friedrich Bauer Foundation |
    1000 Förderprogramm -
    1000 Fördernummer -
  3. 1000 joinedFunding-child
    1000 Förderer Chinese Government Scholarship |
    1000 Förderprogramm -
    1000 Fördernummer -
  4. 1000 joinedFunding-child
    1000 Förderer Dutch Cardiovascular Alliance |
    1000 Förderprogramm -
    1000 Fördernummer -
  5. 1000 joinedFunding-child
    1000 Förderer Klinikum der Universität München |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 @id frl:6515607.rdf
1000 Erstellt am 2025-07-04T16:05:55.274+0200
1000 Erstellt von 322
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1000 Zuletzt bearbeitet 2025-08-15T19:53:03.055+0200
1000 Objekt bearb. Fri Aug 15 19:53:03 CEST 2025
1000 Vgl. frl:6515607
1000 Oai Id
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