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Tanshinone IIA protects against heart failure post-myocardial infarction via AMPKs/mTOR-dependent autophagy pathway
Xuefeng Zhang, Qiyan Wang, Xiaoping Wang, Xu Chen, Mingyan Shao, Qian Zhang, Dongqing Guo, Wu Yan, Chun Li, Wei Wang, Yong Wang
Biomedicine & Pharmacotherapy · 2019 · ▲ 167 citations
Deregulated nutrient-sensing
Altered intercellular communication
Disabled macroautophagy
Rapamycin / mTOR inhibition
Cell culture / in vitro
In vitro
Abstract
Heart failure (HF) leads to an increase in morbidity and mortality globally. Tanshinone IIA is an important traditional Chinese medicine monomer and has been shown to have remarkable protective effect against HF. Autophagy(definition) is critically involved in the progression of HF. The effect of Tanshinone IIA on autophagy has not been clarified yet. In this study, left anterior descending (LAD) ligation was used to induce HF model and a hydrogen peroxide-(H 2 O 2 -)-induced H9C2 cell injury model was established. in vivo , echocardiography results showed that Tanshinone IIA could significantly improve heart function. Western Blot result showed that Tanshinone IIA treatment enhanced autophagy and regulated expressions of key autophagy-related molecules, including protein 1 light chain 3 (LC3), p62 and Beclin1. Tanshinone IIA also inhibited apoptosis and regulated expressions of key apoptotic protein, including B cell lymphoma-2 (Bcl-2) and Bcl-2 Associated X Protein (Bax) and cleaved caspase-3 and -7. Further experiments demonstrated that the effects of Tanshinone IIA were mediated through upregulation of AMP-activated protein kinase (AMPK) and downregulation of mammalian target of mTOR(definition)-inhibiting drug studied for extending healthspan and lifespan." style="text-decoration:underline dotted; text-underline-offset:2px; cursor:help;">rapamycin(definition) (mTOR) simultaneously. The mTOR agonist MHY1485 could abrogate the therapeutic effect of Tanshinone IIA in vitro . In conclusion, Tanshinone IIA protects cardiomyocytes and improves cardiac function by inhibiting apoptosis and inducing autophagy via activation of the AMPK-mTOR signaling pathway.
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Provenance
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- DOI
- 10.1016/j.biopha.2019.108599
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- 2026-08-03 MST
Cite this
APA
Zhang, X., Wang, Q., Wang, X., Chen, X., Shao, M., Zhang, Q., Guo, D., Yan, W., Li, C., Wang, W., & Wang, Y. (2019). Tanshinone IIA protects against heart failure post-myocardial infarction via AMPKs/mTOR-dependent autophagy pathway. <em>Biomedicine & Pharmacotherapy</em>. https://doi.org/10.1016/j.biopha.2019.108599
Vancouver
Zhang X, Wang Q, Wang X, Chen X, Shao M, Zhang Q, et al. Tanshinone IIA protects against heart failure post-myocardial infarction via AMPKs/mTOR-dependent autophagy pathway. Biomedicine & Pharmacotherapy. 2019. doi:10.1016/j.biopha.2019.108599.
BibTeX
@article{xuefeng2019Tanshi,
title = {Tanshinone IIA protects against heart failure post-myocardial infarction via AMPKs/mTOR-dependent autophagy pathway},
author = {Xuefeng Zhang and Qiyan Wang and Xiaoping Wang and Xu Chen and Mingyan Shao and Qian Zhang and Dongqing Guo and Wu Yan and Chun Li and Wei Wang and Yong Wang},
journal = {Biomedicine & Pharmacotherapy},
year = {2019},
doi = {10.1016/j.biopha.2019.108599},
}
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