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J Biochem Mol Toxicol ; 38(10): e23861, 2024 Oct.
Article in English | MEDLINE | ID: mdl-39305037

ABSTRACT

Doxorubicin (DOX) is an anthracycline antibiotic widely employed to treat carcinoma. Nevertheless, severe cardiotoxic side effects restrict its clinical use. Esculetin, a natural flavonoid, is found abundantly in plants. This study evaluated the protective effects of esculetin against DOX-induced hepatotoxicity in rat livers. Forty-eight rats were randomly divided into six groups with eight rats in each group: control (I), DOX (II), esculetin (III, 50 mg/kg), esculetin (IV, 100 mg/kg), DOX+esculetin 50 (V, DOX+esculetin 50 mg/kg), and DOX+esculetin 100 (VI, DOX+esculetin 100 mg/kg). The administration of esculetin effectively mitigated alterations in the measured biochemical parameters induced by DOX. Gene expression analyses demonstrated that esculetin treatment significantly reduced the DOX-induced expression of Foxo1, Hspa1a, Hsp4a, Hsp5a, Casp3, and Casp9 while increasing the DOX-induced expression of Foxo3. These findings suggest that esculetin, with its antioxidant and anti-inflammatory effects, might be a therapeutic option for protecting against DOX-induced hepatotoxicity.


Subject(s)
Chemical and Drug Induced Liver Injury , Doxorubicin , Umbelliferones , Animals , Doxorubicin/adverse effects , Doxorubicin/toxicity , Umbelliferones/pharmacology , Rats , Male , Chemical and Drug Induced Liver Injury/metabolism , Chemical and Drug Induced Liver Injury/prevention & control , Chemical and Drug Induced Liver Injury/drug therapy , Liver/drug effects , Liver/metabolism , Liver/pathology , Heat-Shock Proteins/metabolism , Heat-Shock Proteins/genetics , Forkhead Transcription Factors/metabolism , Caspases/metabolism , Antibiotics, Antineoplastic/toxicity , Antibiotics, Antineoplastic/adverse effects , Signal Transduction/drug effects
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