Protective Effects of
Animals
Mice
Rats
Apoptosis
Cardiotoxicity
/ drug therapy
Doxorubicin
/ toxicity
Heme Oxygenase (Decyclizing)
/ metabolism
Heme Oxygenase-1
/ metabolism
Membrane Proteins
/ metabolism
Mitochondria
/ metabolism
Myocytes, Cardiac
/ metabolism
NF-E2-Related Factor 2
/ metabolism
Oxidative Stress
Polyporaceae
Proto-Oncogene Proteins c-akt
/ metabolism
Signal Transduction
TOR Serine-Threonine Kinases
/ metabolism
Journal
Oxidative medicine and cellular longevity
ISSN: 1942-0994
Titre abrégé: Oxid Med Cell Longev
Pays: United States
ID NLM: 101479826
Informations de publication
Date de publication:
2022
2022
Historique:
received:
24
02
2022
revised:
12
04
2022
accepted:
14
05
2022
entrez:
13
6
2022
pubmed:
14
6
2022
medline:
15
6
2022
Statut:
epublish
Résumé
Clinical outcomes for doxorubicin (Dox) are limited by its cardiotoxicity but a combination of Dox and agents with cardioprotective activities is an effective strategy to improve its therapeutic outcome. Natural products provide abundant resources to search for novel cardioprotective agents.
Identifiants
pubmed: 35693699
doi: 10.1155/2022/9266178
pmc: PMC9177334
doi:
Substances chimiques
Doxorubicin
80168379AG
Heme Oxygenase (Decyclizing)
EC 1.14.14.18
Heme Oxygenase-1
EC 1.14.14.18
Hmox1 protein, mouse
EC 1.14.14.18
Hmox1 protein, rat
EC 1.14.14.18
Membrane Proteins
0
mTOR protein, rat
EC 2.7.1.1
NF-E2-Related Factor 2
0
Proto-Oncogene Proteins c-akt
EC 2.7.11.1
TOR Serine-Threonine Kinases
EC 2.7.11.1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
9266178Informations de copyright
Copyright © 2022 Jingjing Li et al.
Déclaration de conflit d'intérêts
The authors declare no conflict of interest.
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