Key result
Oral fucoidan supplementation protected against doxorubicin-induced cardiotoxicity in mice by reducing oxidative stress and preventing mitochondrial function injury.
Why the study?
Doxorubicin use is limited by dose-dependent cardiotoxicity driven by cardiomyocyte ROS accumulation, prompting exploration of the protective role and mechanism of fucoidan.
Does oral fucoidan supplement prevent doxorubicin-induced cardiotoxicity in mice?
Does oral fucoidan supplement prevent doxorubicin-induced cardiotoxicity in mice?
Oral fucoidan supplementation protects against doxorubicin-induced cardiotoxicity in mice by reducing oxidative stress and preserving mitochondrial function.
Fucoidan may mitigate doxorubicin cardiotoxicity via antioxidant effects in preclinical models; leaves open clinical translation.
Doxorubicin (DOXO) is a potent chemotherapeutic drug widely used to treat various cancers. However, its clinical application is limited due to serious adverse effects on dose-dependent cardiotoxicity. Although the underlying mechanism has not been fully clarified, DOXO-induced cardiotoxicity has been mainly attributed to the accumulation of reactive oxygen species (ROS) in cardiomyocytes. Fucoidan, as a kind of sulphated polysaccharide existing in numerous brown seaweed, has potent anti-oxidant, immune-regulatory, anti-tumor, anti-coagulate and anti-viral activities. Here, we explore the potential protective role and mechanism of fucoidan in DOXO-induced cardiotoxicity in mice. Our results show that oral fucoidan supplement exerts potent protective effects against DOXO-induced cardiotoxicity by reducing oxidative stress and preventing mitochondrial function injury. The improved effect of fucoidan on DOXO-induced cardiotoxicity was evaluated by echocardiography, cardiac myocytes size and cardiac fibrosis analysis, and the expression of genes related to cardiac dysfunction and remodeling. Fucoidan reduced the ROS content and the MDA levels but enhanced the activity of antioxidant enzymes GSH-PX and SOD in the mouse serum in a DOXO-induced cardiotoxicity model. In addition, fucoidan also increased the ATP production capacity and restored the levels of a mitochondrial respiratory chain complex in heart tissue. Collectively, this study highlights fucoidan as a potential polysaccharide for protecting against DOXO-induced cardiovascular diseases.
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Ji et al. (2022) studied Doxorubicin-induced cardiotoxicity. Oral fucoidan supplement was evaluated on Cardiotoxicity (evaluated by echocardiography, cardiac myocytes size, cardiac fibrosis, and gene expression). Oral fucoidan supplementation protected against doxorubicin-induced cardiotoxicity in mice by reducing oxidative stress and preventing mitochondrial function injury.
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