Protective effects of gallic acid on doxorubicin-induced cardiotoxicity; an experimantal study.
Animals
Cyclooxygenase 2
/ metabolism
Cytoprotection
/ drug effects
Dose-Response Relationship, Drug
Doxorubicin
/ adverse effects
Drug Interactions
Gallic Acid
/ pharmacology
Gene Expression Regulation, Enzymologic
/ drug effects
Heart
/ drug effects
Malondialdehyde
/ metabolism
Rats
Tumor Necrosis Factor-alpha
/ metabolism
Doxorubicin
antioxidant
cardiotoxicity
cytokins
gallic acid
rat
Journal
Archives of physiology and biochemistry
ISSN: 1744-4160
Titre abrégé: Arch Physiol Biochem
Pays: England
ID NLM: 9510153
Informations de publication
Date de publication:
Jun 2021
Jun 2021
Historique:
pubmed:
27
6
2019
medline:
27
8
2021
entrez:
27
6
2019
Statut:
ppublish
Résumé
The present study aims to examine the possible beneficial effects of gallic acid (GA) against doxorubicin-induced cardiotoxicity in the experimental model. Rats were weighed and divided into groups. Groups as following; control, gallic acid (GA), doxorubicin (DOX) and GA + DOX groups. At the end of the experiment, rats were sacrificed and heart tissue removed. The tissues were analysed in terms of biochemical (MDA, SOD, CAT, GSH, GPx), pathological (hyaline degeneration, Zenkerin necrosis, hyperaemia) and immunohistochemical (TNF-α, Cox-2). MDA level decreased and antioxidant enzyme activities increased in GA + DOX group compared to doxorubicin group. TNF-α, Cox-2 expression levels were severe in the DOX group. Also, pathologic tissue damage in heart tissue increased due to doxorubicin. Additionally, pathologic tissue damage and TNF-α, Cox-2 expression levels decreased in GA + DOX group. According to our findings, GA has protective effect against doxorubicin-induced cardiotoxicity.
Identifiants
pubmed: 31240966
doi: 10.1080/13813455.2019.1630652
doi:
Substances chimiques
Tumor Necrosis Factor-alpha
0
Malondialdehyde
4Y8F71G49Q
Gallic Acid
632XD903SP
Doxorubicin
80168379AG
Cyclooxygenase 2
EC 1.14.99.1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM