Literature DB >> 32068018

Multi-walled carbon nanotubes exacerbate doxorubicin-induced cardiotoxicity by altering gut microbiota and pulmonary and colonic macrophage phenotype in mice.

Xiaoxiao Liu1, Yanzhuo Liu1, Xuewei Chen2, Chenlong Wang3, Xuehan Chen1, Wen Liu1, Keqing Huang1, Honglei Chen4, Jing Yang5.   

Abstract

Epidemiologic studies show that the levels of air pollutants and particulate matter are positively associated with the morbidity and mortality of cardiovascular diseases. Here we demonstrate that the intratracheal instillation of multi-walled carbon nanotubes (MWCNTs), a standard fine particle, exacerbate doxorubicin (DOX)-induced cardiotoxicity in mice through altering gut microbiota and pulmonary and colonic macrophage phenotype. MWCNTs (25 μg/kg per day, 5 days a week for 3 weeks) promoted cardiotoxicity and apoptosis in the DOX (2 mg/kg, twice a week for 5 weeks)-treated C57BL/6 mice. MWCNTs exaggerated DOX-induced gut microbiota dysbiosis characterized by the increased abundances of Helicobacteraceae and Coriobacteriaceae. In addition, MWCNTs promoted DOX-induced M1-like polarization of colonic macrophages with an increase in TNF-α, IL-1β and CC chemokine ligand 2 in peripheral blood. Importantly, treatment with the antibiotics attenuated MWCNTs plus DOX-induced apoptosis of cardiomyocytes and M1-like polarization of colonic macrophages. The fecal microbiota transplantation demonstrated that MWCNTs exaggerated DOX-induced cardiotoxicity with M1-like polarization of colonic macrophages. The conditioned medium from MWCNTs-treated pulmonary macrophages promoted DOX-induced gut microbiota dysbiosis and colonic macrophage polarization. Furthermore, the co-culture of macrophages and fecal bacteria promoted M1-like macrophage polarization and their production of TNF-α and IL-1β, and thereby exacerbated the effects of MWCNTs. Moreover, IL-1β and TNF-α blockade, either alone or in combination attenuated MWCNTs-exacerbated cardiotoxicity. In summary, MWCNTs exacerbate DOX-induced cardiotoxicity in mice through gut microbiota and pulmonary and colonic macrophage interaction. Our findings identify a novel mechanism of action of inhaled particle-driven cardiotoxicity.
Copyright © 2020 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cardiotoxicity; Colonic macrophage; Doxorubicin; Gut microbiota; MWCNTs

Year:  2020        PMID: 32068018     DOI: 10.1016/j.tox.2020.152410

Source DB:  PubMed          Journal:  Toxicology        ISSN: 0300-483X            Impact factor:   4.221


  3 in total

1.  Butyric Acid Ameliorates Myocardial Fibrosis by Regulating M1/M2 Polarization of Macrophages and Promoting Recovery of Mitochondrial Function.

Authors:  Xiaogang Li; Ruixuan Li; Nana You; Xiexiong Zhao; Jiaying Li; Weihong Jiang
Journal:  Front Nutr       Date:  2022-05-18

2.  Prevotellaceae produces butyrate to alleviate PD-1/PD-L1 inhibitor-related cardiotoxicity via PPARα-CYP4X1 axis in colonic macrophages.

Authors:  Yaxin Chen; Yanzhuo Liu; Yang Wang; Xuewei Chen; Chenlong Wang; Xuehan Chen; Xi Yuan; Lilong Liu; Jing Yang; Xiaoyang Zhou
Journal:  J Exp Clin Cancer Res       Date:  2022-01-03

3.  Involvement of Abnormal Gut Microbiota Composition and Function in Doxorubicin-Induced Cardiotoxicity.

Authors:  Jie Huang; Shanshan Wei; Chuanhao Jiang; Zijun Xiao; Jian Liu; Weijun Peng; Bikui Zhang; Wenqun Li
Journal:  Front Cell Infect Microbiol       Date:  2022-02-25       Impact factor: 5.293

  3 in total

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