Open Access

Multi‑omics analysis of right ventricles in rat models of pulmonary arterial hypertension: Consideration of mitochondrial biogenesis by chrysin

  • Authors:
    • Takayuki Kobayashi
    • Jun-Dal Kim
    • Akira Naito
    • Asako Yanagisawa
    • Takayuki Jujo‑Sanada
    • Yoshitoshi Kasuya
    • Yoshimi Nakagawa
    • Seiichiro Sakao
    • Koichiro Tatsumi
    • Takuji Suzuki
  • View Affiliations

  • Published online on: March 21, 2022     https://doi.org/10.3892/ijmm.2022.5124
  • Article Number: 69
  • Copyright: © Kobayashi et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

In pulmonary arterial hypertension (PAH), right ventricular failure is accompanied by metabolic alterations in cardiomyocytes, which may be due to mitochondrial dysfunction and decreased energy production. Chrysin (CH) is a phytochemical with pharmacological activity that is involved in the regulation of mitochondrial biogenesis. The present study investigated the role of CH in the right ventricle (RV) by analyzing the cardiac transcriptome and metabolome of a SU5416(a vascular endothelial growth factor receptor blocker, /hypoxia (Su/Hx) rat model of PAH. RNA‑sequencing of the RV transcriptome between Su/Hx, Su/Hx with CH (Su/Hx + CH) and control groups, extracellular matrix (ECM) organization and ECM‑receptor interaction‑associated genes were upregulated in the RV of Su/Hx but not Su/Hx + CH rats. Furthermore, expression of mitochondrial function‑, energy production‑, oxidative phosphorylation‑ and tricarboxylic acid (TCA) cycle‑associated genes was decreased in the RV of Su/Hx rats; this was reverse by CH. Metabolomic profiling analysis of Su/Hx and Su/Hx + CH rats showed no significant changes in glycolysis, TCA cycle, glutathione, NADH or NADPH. By contrast, in the RV of Su/Hx rats, decreased adenylate energy charge was partially reversed by CH administration, suggesting that CH was involved in the improvement of mitochondrial biogenesis. Reverse transcription‑quantitative PCR analysis revealed that expression of peroxisome proliferator‑activated receptor γ, a master regulator of fatty acid metabolism and mitochondrial biogenesis, was increased in the RV of Su/Hx + CH rats. CH ameliorated cardiac abnormality, including cardiac fibrosis, RV hypertrophy and PH. The present study suggested that CH altered patterns of gene expression and levels of mitochondrial metabolites in cardiomyocytes, thus improving RV dysfunction in a Su/Hx PAH rat model.
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May-2022
Volume 49 Issue 5

Print ISSN: 1107-3756
Online ISSN:1791-244X

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Spandidos Publications style
Kobayashi T, Kim J, Naito A, Yanagisawa A, Jujo‑Sanada T, Kasuya Y, Nakagawa Y, Sakao S, Tatsumi K, Suzuki T, Suzuki T, et al: Multi‑omics analysis of right ventricles in rat models of pulmonary arterial hypertension: Consideration of mitochondrial biogenesis by chrysin. Int J Mol Med 49: 69, 2022
APA
Kobayashi, T., Kim, J., Naito, A., Yanagisawa, A., Jujo‑Sanada, T., Kasuya, Y. ... Suzuki, T. (2022). Multi‑omics analysis of right ventricles in rat models of pulmonary arterial hypertension: Consideration of mitochondrial biogenesis by chrysin. International Journal of Molecular Medicine, 49, 69. https://doi.org/10.3892/ijmm.2022.5124
MLA
Kobayashi, T., Kim, J., Naito, A., Yanagisawa, A., Jujo‑Sanada, T., Kasuya, Y., Nakagawa, Y., Sakao, S., Tatsumi, K., Suzuki, T."Multi‑omics analysis of right ventricles in rat models of pulmonary arterial hypertension: Consideration of mitochondrial biogenesis by chrysin". International Journal of Molecular Medicine 49.5 (2022): 69.
Chicago
Kobayashi, T., Kim, J., Naito, A., Yanagisawa, A., Jujo‑Sanada, T., Kasuya, Y., Nakagawa, Y., Sakao, S., Tatsumi, K., Suzuki, T."Multi‑omics analysis of right ventricles in rat models of pulmonary arterial hypertension: Consideration of mitochondrial biogenesis by chrysin". International Journal of Molecular Medicine 49, no. 5 (2022): 69. https://doi.org/10.3892/ijmm.2022.5124