Akkermansia muciniphila ameliorates doxorubicin-induced cardiotoxicity by regulating PPARα-dependent mitochondrial biogenesis

Doxorubicin (DOX) is a key chemotherapeutic agent but is also a leading cause of DOX-induced cardiotoxicity (DIC), limiting its clinical use. Akkermansia muciniphila (A. muciniphila), known for its benefits as a probiotic in treating metabolic syndrome, has uncertain effects in the context of DIC. Here, 16S rRNA sequencing of fecal samples from anthracycline-treated patients and DIC mice revealed marked depletion of A. muciniphila. Cardiac transcriptomics, supported by in vitro experiments, showed that A. muciniphila colonization improved mitochondrial function and alleviated DIC by activating the PPARα/PGC1α signaling pathway in both normal and antibiotic-treated C57BL/6 mice. Further analysis uncovered a restructured microbiome-metabolome network following A. muciniphila administration, which contributed to DIC protection. Notably, A. muciniphila supplementation increased serum levels of the tryptophan metabolite indole-3-propionic acid (IPA), which binds to the cardiac aryl hydrocarbon receptor (AhR), leading to the activation of the PPARα/PGC1α signaling pathway. In conclusion, our study sheds light on the potential of A. muciniphila as a probiotic in mitigating DIC.

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Publication Details

Journal
npj Biofilms and Microbiomes
Published
2025-05-23
DOI
https://doi.org/10.1038/s41522-025-00712-y
Citations
4
Primary Topic
Chemotherapy-induced cardiotoxicity and mitigation
Type
article
Field-Weighted Citation Impact
5.55

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article

Akkermansia muciniphila ameliorates doxorubicin-induced cardiotoxicity by regulating PPARα-dependent mitochondrial biogenesis

Lili Xu, Jiedong Zhou, Yongfei Song, Jiangfang Lian et al.
4 citations
npj Biofilms and Microbiomes
Chemotherapy-induced cardiotoxicity and mitigation
5.55
article

Akkermansia muciniphila ameliorates doxorubicin-induced cardiotoxicity by regulating PPARα-dependent mitochondrial biogenesis

Lili Xu, Jiedong Zhou, Yongfei Song, Jiangfang Lian, Hui Lin, Xiaohong Yu, Shangjing Guo, Zuoquan Zhong, Xian Shao, Ping Wang, Dan Li, Fei Chen, Liping Meng, Jufang Chi, Ling‐Yan He, Haodi Gu
article en
4 citations

Abstract

Doxorubicin (DOX) is a key chemotherapeutic agent but is also a leading cause of DOX-induced cardiotoxicity (DIC), limiting its clinical use. Akkermansia muciniphila (A. muciniphila), known for its benefits as a probiotic in treating metabolic syndrome, has uncertain effects in the context of DIC. Here, 16S rRNA sequencing of fecal samples from anthracycline-treated patients and DIC mice revealed marked depletion of A. muciniphila. Cardiac transcriptomics, supported by in vitro experiments, showed that A. muciniphila colonization improved mitochondrial function and alleviated DIC by activating the PPARα/PGC1α signaling pathway in both normal and antibiotic-treated C57BL/6 mice. Further analysis uncovered a restructured microbiome-metabolome network following A. muciniphila administration, which contributed to DIC protection. Notably, A. muciniphila supplementation increased serum levels of the tryptophan metabolite indole-3-propionic acid (IPA), which binds to the cardiac aryl hydrocarbon receptor (AhR), leading to the activation of the PPARα/PGC1α signaling pathway. In conclusion, our study sheds light on the potential of A. muciniphila as a probiotic in mitigating DIC.

npj Biofilms and MicrobiomesVol. 11(1)
Ningbo University (CN), Shaoxing University (CN), Wenzhou Medical University (CN), Ningbo Medical Center Lihuili Hospital (CN), Shaoxing No.6 People's Hospital (CN), Second Affiliated Hospital of Zhejiang University (CN), Shaoxing People's Hospital (CN)
National Natural Science Foundation of China, Natural Science Foundation of Zhejiang Province
Zero hunger
Openalex Percentile: Top 4%
Chemotherapy-induced cardiotoxicity and mitigation
5.55
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