Barbeya oleoides leaf extract significantly reduced oxidative stress and improved cardiac function in rats with doxorubicin-induced cardiotoxicity at doses of 100 to 400 mg/kg.
Does Barbeya oleoides leaf extract mitigate doxorubicin-induced cardiotoxicity in rats?
Barbeya oleoides leaf extract demonstrates cardioprotective effects against doxorubicin-induced cardiotoxicity in a rat model through antioxidant, anti-inflammatory, and anti-apoptotic mechanisms.
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Abstract Doxorubicin (DOX) is a renowned chemotherapeutic agent that belongs to the class of anthracycline antibiotics. The cardioprotective effect of Barbeya oleoides leaf extract were assessed in DOX-induced cardiotoxicity utilising in-vivo methods. Following the administration of DOX (10 mg/kg, i.p.), cardiotoxicity was caused. Apoptotic indicators (Caspase 3 and 9), cardiac markers (LDH, CK-MB, BNP, cTnI, and cTnT), inflammatory cytokines (IL-1β, TNF-α, and IL-6), and oxidative stress markers (MDA, GSH, SOD, GR, GPx, and CAT) were evaluated. Furthermore, histological evaluation was performed to analyse and appraise alterations in the structural integrity of heart tissue. Rats given DOX showed a substantial increase in lipid peroxidation (LPO) levels, which were followed by increases in cardiac, inflammatory, and apoptotic markers as well as a decrease in antioxidant enzymes. LPO, cardiac, inflammatory, and apoptotic indicators were significantly reduced in groups 3, 4, and 5 after receiving B. oleoides leaf extract in doses of 100, 200, and 400 mg/kg. Additionally, it has shown a notable increase in GSH and antioxidant enzyme levels. Additionally, histopathology revealed that DOX also caused abnormalities in the structural integrity of cardiac tissue, including the creation of vacuoles, a large uncondensed nucleus, and a myofibril loss. Barbeya oleoides extract improved structural integrity and dampen the inflammatory cells infiltration in cardiac tissue.
ALAM et al. (Thu,) reported a other. Barbeya oleoides leaf extract significantly reduced oxidative stress and improved cardiac function in rats with doxorubicin-induced cardiotoxicity at doses of 100 to 400 mg/kg.
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