Thorac Cardiovasc Surg 2024; 72(S 01): S1-S68
DOI: 10.1055/s-0044-1780616
Monday, 19 February
Molekulare Herzchirurgie: Vom Mechanismus zur Funktion

Comparison of the Stage-Dependent Mitochondrial Changes in Response to Pressure Overload between the Diseased Right and Left Ventricle in the Rat

B. Niemann
1   Klinik für Herz-, Kinderherz- und Gefäßchirurgie, UKGM Giessen, Rudolf-Buchheim-Straße 7, Giessen, Deutschland
,
L. Li
2   Physiologisches Institut Justus Liebig Universität Giessen, Aulweg 129 35457 Giessen, Giessen, Germany, Deutschland
,
C. Mühlfeld
3   Medizinische Hochschule Hannover, Hannover, Deutschland
,
L. Jurida
4   Rudolf-Buchheim-Straße 7, Giessen, Deutschland
,
R. Schulz
2   Physiologisches Institut Justus Liebig Universität Giessen, Aulweg 129 35457 Giessen, Giessen, Germany, Deutschland
,
M. Mayr
5   King's College, London, United Kingdom
,
M.L. Schmitz
6   Institute of Biochemistry, Justus-Liebig-University, Gießen, Deutschland
,
M. Kracht
7   Rudolf Buchheim Institut für Pharmakologie, Justus-Liebig Universität Giessen, Gießen, Deutschland
,
S. Rohrbach
2   Physiologisches Institut Justus Liebig Universität Giessen, Aulweg 129 35457 Giessen, Giessen, Germany, Deutschland
› Institutsangaben

Background: The right ventricle (RV) differs developmentally, anatomically and functionally from the left ventricle (LV). Therefore, characteristics of LV adaptation to chronic pressure overload cannot easily be extrapolated to the RV. Mitochondrial abnormalities are considered a crucial contributor in heart failure (HF), but have never been compared directly between RV and LV tissues and cardiomyocytes.

Methods: To identify ventricle-specific mitochondrial molecular and functional signatures, we established rat models with two slowly developing disease stages (compensated and decompensated) in response to pulmonary artery banding (PAB) or ascending aortic banding (AOB). Genome-wide transcriptomic and proteomic analyses were used to identify differentially expressed mitochondrial genes and proteins and were accompanied by a detailed characterization of mitochondrial function and morphology.

Results: Two clearly distinguishable disease stages, which culminated in a comparable systolic impairment of the respective ventricle, were observed. Mitochondrial respiration was similarly impaired at the decompensated stage, while respiratory chain activity or mitochondrial biogenesis were more severely deteriorated in the failing LV. Bioinformatics analyses of the RNAseq. and proteomic data sets identified specifically deregulated mitochondrial components and pathways. Although the top regulated mitochondrial genes and proteins differed between the RV and LV, the overall changes in tissue and cardiomyocyte gene expression were highly similar.

Conclusion: Mitochondrial dysfunction contributes to disease progression in right and left heart failure. Ventricle-specific differences in mitochondrial gene and protein expression are mostly related to the extent of observed changes, suggesting that despite developmental, anatomical and functional differences mitochondrial adaptations to chronic pressure overload are comparable in both ventricles.



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Artikel online veröffentlicht:
13. Februar 2024

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