Inflammation suppression in doxorubicin-induced cardiotoxicity: natural compounds as therapeutic options

Doxorubicin (DOX) is a potent chemotherapeutic agent; however, the accompanying cardiotoxicity is a significant complication of the usefulness of treatment with DOX. Multiple mechanisms have been suggested for this often fatal side effect, one of which is inflammation. Several pathways with differen...

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Veröffentlicht in:Naunyn-Schmiedeberg's archives of pharmacology 2021-10, Vol.394 (10), p.2003-2011
Hauptverfasser: Yarmohammadi, Fatemeh, Karbasforooshan, Hedyieh, Hayes, A. Wallace, Karimi, Gholamreza
Format: Artikel
Sprache:eng
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Zusammenfassung:Doxorubicin (DOX) is a potent chemotherapeutic agent; however, the accompanying cardiotoxicity is a significant complication of the usefulness of treatment with DOX. Multiple mechanisms have been suggested for this often fatal side effect, one of which is inflammation. Several pathways with different targets have been reported to result in DOX-induced heart inflammation. Some natural occurring compounds (NCs) have been reported to interact with the DOX-induced cardiotoxicity through targeting one or more of several pathways, including the Nrf2/NF-kB, TLR-4/NF-kB, MAPK/NF-kB, and NLRP3 inflammasome pathways. This article reviews several of these pathways and the potential protective effect of some NCs against the cardiac inflammation induced by DOX.
ISSN:0028-1298
1432-1912
DOI:10.1007/s00210-021-02132-z