Jujuboside A attenuates norepinephrine-induced apoptosis of H9c2 cardiomyocytes by modulating MAPK and AKT signaling pathways

  • Authors:
    • Chang‑Rong Wan
    • Dan‑Dan Han
    • Jian‑Qin Xu
    • Peng Yin
    • Xiao‑Long Xu
    • Chen Mei
    • Feng‑Hua Liu
    • Zhao‑Fei Xia
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  • Published online on: November 2, 2017     https://doi.org/10.3892/mmr.2017.7938
  • Pages: 1132-1140
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Abstract

Cardiomyocyte apoptosis is closely associated with the pathogenesis of heart failure. Jujuboside A (JUA) is a type of saponin isolated from the seeds of Zizyphus jujuba. In traditional Chinese medicine, it is believed that JUA possesses multiple biological effects, including antianxiety, antioxidant and anti‑inflammatory activities. The present study aimed to evaluate the effects of JUA on norepinephrine (NE)‑induced apoptosis of H9c2 cells and to investigate its underlying mechanisms. Rat H9c2 cardiomyocytes were pretreated with JUA and were then exposed to NE as an in vitro model of myocardial apoptosis. A cell viability assay, scanning electron microscopy, transmission electron microscopy, flow cytometry assay, acridine orange/ethidium bromide staining, reverse transcription‑quantitative polymerase chain reaction and western blotting, all revealed that NE induced H9c2 cell apoptosis. The results demonstrated that NE inhibited cell viability, and enhanced cell damage and apoptosis of H9c2 cells. Conversely, pretreatment with JUA was able to reverse NE‑induced decreased cell viability and increased apoptosis. Furthermore, JUA suppressed upregulation of the B‑cell lymphoma 2 (Bcl‑2)‑associated X protein/Bcl‑2 ratio, and inhibited the increased protein expression levels of cleaved caspase‑3 and cleaved caspase‑9 following NE exposure. However, the protein expression levels of cleaved caspase‑12 and cleaved caspase‑8 were not significantly altered following exposure to NE or JUA pretreatment. In addition, in JUA‑pretreated cells, the protein expression levels of phosphorylated (p)‑p38 and p‑c‑Jun N‑terminal kinase were downregulated compared with in NE‑treated cells. Furthermore, JUA regulated the activation of extracellular signal‑regulated kinase (ERK) in NE‑treated cells and significantly increased the expression levels of p‑AKT. Taken together, these data suggested that JUA may protect against NE‑induced apoptosis of cardiomyocytes via modulation of the mitogen‑activated protein kinase and AKT signaling pathways. Therefore, JUA may be considered a potential therapeutic strategy for the treatment of heart disease.
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January-2018
Volume 17 Issue 1

Print ISSN: 1791-2997
Online ISSN:1791-3004

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Spandidos Publications style
Wan CR, Han DD, Xu JQ, Yin P, Xu XL, Mei C, Liu FH and Xia ZF: Jujuboside A attenuates norepinephrine-induced apoptosis of H9c2 cardiomyocytes by modulating MAPK and AKT signaling pathways. Mol Med Rep 17: 1132-1140, 2018
APA
Wan, C., Han, D., Xu, J., Yin, P., Xu, X., Mei, C. ... Xia, Z. (2018). Jujuboside A attenuates norepinephrine-induced apoptosis of H9c2 cardiomyocytes by modulating MAPK and AKT signaling pathways. Molecular Medicine Reports, 17, 1132-1140. https://doi.org/10.3892/mmr.2017.7938
MLA
Wan, C., Han, D., Xu, J., Yin, P., Xu, X., Mei, C., Liu, F., Xia, Z."Jujuboside A attenuates norepinephrine-induced apoptosis of H9c2 cardiomyocytes by modulating MAPK and AKT signaling pathways". Molecular Medicine Reports 17.1 (2018): 1132-1140.
Chicago
Wan, C., Han, D., Xu, J., Yin, P., Xu, X., Mei, C., Liu, F., Xia, Z."Jujuboside A attenuates norepinephrine-induced apoptosis of H9c2 cardiomyocytes by modulating MAPK and AKT signaling pathways". Molecular Medicine Reports 17, no. 1 (2018): 1132-1140. https://doi.org/10.3892/mmr.2017.7938