Key result
Yellow wine polyphenols attenuate doxorubicin-induced cardiotoxicity in rats by improving cardiac function and reducing apoptosis.
Why the study?
Dietary polyphenols interact with gut microbiota and may prevent cardiovascular diseases, but their role in modulating gut microbiota to protect against doxorubicin-induced cardiotoxicity is unclear.
Answers are grounded in this paper and cite their sources.
May protect against DOX cardiotoxicity via microbiota in rats; hypothesis-generating and should not change practice.
Background: Dietary polyphenols help to prevent cardiovascular diseases, and interactions between polyphenols and gut microbiota are known to exist. In this study, we speculated that gut microbiota-mediated metabolite regulation might contribute to the anticardiotoxic effects of yellow wine polyphenolic compound (YWPC) in doxorubicin (DOX)-treated rats. Methods: 16S-rDNA sequencing was performed to analyze the effects of YWPC on the gut microbiota in DOX-treated rats (n=6). Antibiotics were used to investigate the contribution of the altered microbiome to the role of YWPC (n=6). Plasma metabolomics were also analyzed by untargeted gas chromatography-mass spectrometry systems. Results: YWPC ameliorated DOX-mediated cardiotoxicity, as evidenced by increased cardiac and mitochondrial function and reduced levels of inflammation and myocardial apoptosis ( P <0.05 for all). The low abundance of Escherichia – Shigella , Dubosiella , and Allobaculum , along with enrichment of Muribaculaceae_unclassified , Ralstonia , and Rikenellaceae_RC9_gut_group in the gut, suggested that YWPC ameliorated DOX-induced microbial dysbiosis. YWPC also influenced the levels of metabolites altered by DOX, resulting in lower arachidonic acid and linoleic acid metabolism and higher tryptophan metabolite levels ( P <0.05 for all). Correlational studies indicated that YWPC alleviated DOX-induced inflammation and mitochondrial dysfunction by modulating the gut microbial community and its associated metabolites. Antibiotic treatment exacerbated cardiotoxicity in DOX-treated rats, and its effect on the gut microbiota partly abolished the anticardiotoxic effects of YWPC, suggesting that the microbiota is required for the cardioprotective role of YWPC. Conclusions: YWPC protected against DOX-induced cardiotoxicity in a gut microbiota–dependent manner. This supports the use of dietary polyphenols as a therapeutic approach for the treatment of cardiovascular diseases via microbiota regulation.
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Lin et al. (2021) studied Doxorubicin-induced cardiotoxicity. Yellow wine polyphenolic compound (YWPC) vs. Doxorubicin alone was evaluated on Cardiac and mitochondrial function, inflammation, and myocardial apoptosis (p=<0.05). Yellow wine polyphenolic compound ameliorated doxorubicin-induced cardiotoxicity in rats by improving cardiac function and reducing inflammation and myocardial apoptosis.
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