Right versus left ventricular remodeling in heart failure due to chronic volume overload

0554631 - ÚMG 2022 RIV GB eng J - Článek v odborném periodiku
Havlenová, T. - Škaroupková, P. - Miklovic, M. - Behounek, M. - Chmel, M. - Jarkovská, D. - Švíglerová, J. - Štengl, M. - Kolář, Michal - Novotný, Jiří - Beneš, J. - Červenka, L. - Petrák, J. - Melenovský, V.
Right versus left ventricular remodeling in heart failure due to chronic volume overload.
Scientific Reports. Roč. 11, č. 1 (2021), č. článku 17136. ISSN 2045-2322. E-ISSN 2045-2322
Grant CEP: GA MŠMT(CZ) LM2018131
Výzkumná infrastruktura: ELIXIR-CZ II - 90131
Institucionální podpora: RVO:68378050
Klíčová slova: myosin heavy-chain * pulmonary-hypertension * extracellular-matrix * molecular-mechanisms * loading conditions * gene-expression * cell-adhesion * rats * dysfunction * model
Obor OECD: Biology (theoretical, mathematical, thermal, cryobiology, biological rhythm), Evolutionary biology
Impakt faktor: 4.997, rok: 2021
Způsob publikování: Open access
https://www.nature.com/articles/s41598-021-96618-8

Mechanisms of right ventricular (RV) dysfunction in heart failure (HF) are poorly understood. RV response to volume overload (VO), a common contributing factor to HF, is rarely studied. The goal was to identify interventricular differences in response to chronic VO. Rats underwent aorto-caval fistula (ACF)/sham operation to induce VO. After 24 weeks, RV and left ventricular (LV) functions, gene expression and proteomics were studied. ACF led to biventricular dilatation, systolic dysfunction and hypertrophy affecting relatively more RV. Increased RV afterload contributed to larger RV stroke work increment compared to LV. Both ACF ventricles displayed upregulation of genes of myocardial stress and metabolism. Most proteins reacted to VO in a similar direction in both ventricles, yet the expression changes were more pronounced in RV (p(slope): < 0.001). The most upregulated were extracellular matrix (POSTN, NRAP, TGM2, CKAP4), cell adhesion (NCAM, NRAP, XIRP2) and cytoskeletal proteins (FHL1, CSRP3) and enzymes of carbohydrate (PKM) or norepinephrine (MAOA) metabolism. Downregulated were MYH6 and FAO enzymes. Therefore, when exposed to identical VO, both ventricles display similar upregulation of stress and metabolic markers. Relatively larger response of ACF RV compared to the LV may be caused by concomitant pulmonary hypertension. No evidence supports RV chamber-specific regulation of protein expression in response to VO.
Trvalý link: http://hdl.handle.net/11104/0329326