Abstract |
Doxorubicin- (DOX-) induced cardiomyocyte loss results in irreversible heart failure, which limits the clinical applications of DOX. Currently, there are no drugs that can effectively treat DOX-related cardiotoxicity. Follistatin-like 1 (FSTL1) has been reported to be a transforming growth factor-beta-inducible gene, and FSTL1 supplementation attenuated ischemic injury and cardiac apoptotic loss in mice. However, the effect of FSTL1 on DOX-induced cardiomyopathy has not been elucidated. We aimed to explore whether FSTL1 could prevent DOX-related cardiotoxicity in mice. Mice were intraperitoneally injected with a single dose of DOX to induce acute cardiotoxicity. We used an adeno-associated virus system to overexpress FSTL1 in the heart. DOX administration decreased FSTL1 mRNA and protein expression in the heart and in cells. FSTL1 prevented DOX-related cardiac injury and inhibited cardiac oxidative stress and apoptosis, thereby improving cardiac function in mice. FSTL1 also improved cardiomyocyte contractile functions in vitro. FSTL1 upregulated expression of nuclear factor (erythroid-derived 2)-like 2 (Nrf2) in DOX-treated hearts. FSTL1 was not capable of protecting against these toxic effects in Nrf2-deficient mice. In conclusion, FSTL1 protected against DOX-induced cardiotoxicity via upregulation of Nrf2 expression.
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Authors | Yintao Zhao, Jingjing Sun, Wei Zhang, Meng Peng, Jun Chen, Lu Zheng, Xiangqin Zhang, Haibo Yang, Yuan Liu |
Journal | Oxidative medicine and cellular longevity
(Oxid Med Cell Longev)
Vol. 2020
Pg. 3598715
( 2020)
ISSN: 1942-0994 [Electronic] United States |
PMID | 32831995
(Publication Type: Journal Article)
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Copyright | Copyright © 2020 Yintao Zhao et al. |
Chemical References |
- Follistatin
- NF-E2-Related Factor 2
- Doxorubicin
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Topics |
- Animals
- Cardiomyopathies
(chemically induced)
- Doxorubicin
(adverse effects)
- Follistatin
(pharmacology)
- Male
- Mice
- NF-E2-Related Factor 2
(metabolism)
- Rats
- Up-Regulation
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