Cardioprotective effects of corilagin on doxorubicin induced cardiotoxicity via P13K/Akt and NF-κB signaling pathways in a rat model
Autor: | Ying Lei, Xinwen Gong, Jing Huang, Shengping Lei |
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Rok vydání: | 2021 |
Předmět: |
Necrosis
Health Toxicology and Mutagenesis Apoptosis Inflammation macromolecular substances Pharmacology Toxicology chemistry.chemical_compound Glucosides polycyclic compounds medicine Animals Doxorubicin Cardioprotective Agent Protein kinase B Cardiotoxicity NF-kappa B Hydrolyzable Tannins Rats carbohydrates (lipids) Oxidative Stress chemistry medicine.symptom Proto-Oncogene Proteins c-akt Corilagin Signal Transduction medicine.drug |
Zdroj: | Toxicology Mechanisms and Methods. 32:79-86 |
ISSN: | 1537-6524 1537-6516 |
Popis: | Even though doxorubicin (DOX) is a potential chemotherapeutic drug, its usage is restricted due to its ability to induce cardiac damage. In order to prevent this damage, a potent cardioprotective agent should be associated with DOX treatment. Corilagin is a natural polyphenol tannic acid which unveils enormous pharmacological activities predominantly as an antitumor agent. Hence, the current work is designed to study the precise mechanisms of corilagin upon administration in doxorubicin induced cardiotoxicity in experimental rats. DOX treated rats showed diminished level of blood pressures and heart rate, whereas corilagin along with DOX treatment improved the status. Cardiotoxicity enzymes and biomarkers were found to be increased in the serum of DOX induced rats. Upon treatment, corilagin could reduce the cardiotoxicity enzymes and biomarkers in serum. Histopathological examination of cardiac tissue also revealed the anti-toxic effects of corilagin in contrast to DOX. Injection of DOX in rats showed inflammatory cells infiltration, necrosis and fragmented myofibrils. Corilagin treatment reverted the cardiac histology to near normal. Inflammatory mediators and P13K, Akt, and NF-κB were upregulated in DOX administered rats. Corilagin repressed the levels of P13K, Akt, and NF-κB in DOX induced rats. In the present investigations, corilagin improved cardiac function via reducing injury, inflammation and promoting apoptosis thereby suggesting that corilagin would be recommended for DOX-induced cardiotoxicity. |
Databáze: | OpenAIRE |
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