Key result
Curcumin and beta-carotene attenuate cisplatin-induced cardiotoxicity in preclinical models, with greater protection from curcumin.
Why the study?
Cisplatin is an effective antineoplastic drug but has a cardiotoxic effect, and the protective roles of curcumin and beta-carotene against this cardiotoxicity were evaluated.
Does curcumin or beta-carotene prevent cisplatin-induced cardiotoxicity in a rat model?
Does curcumin or beta-carotene prevent cisplatin-induced cardiotoxicity in a rat model?
Curcumin and beta-carotene demonstrate cardioprotective effects against cisplatin-induced cardiotoxicity in a rat model, with curcumin showing higher efficacy.
Hypothesis-generating for CMN/BC cardioprotection in rat CDDP cardiotoxicity; clinical translation remains untested.
OBJECTIVE: Cisplatin (CDDP) has been known to be an effective antineoplastic drug; however, it has a cardiotoxic effect. Curcumin (CMN) and beta-carotene (BC) have been suggested to protect biological systems against CDDP-induced damage. The current study was conducted to evaluate the possible protective roles of CMN and BC on CDDP-induced cardiotoxicity in rat cardiac tissues. METHODS: A total of 49 adult female Wistar albino rats were equally divided into seven groups as follows: control (no medication), sesame oil (1 mg/kg), CDDP (single dose injection two times as once a week, 5 mg/kg/week), BC (100 mg/kg), CDDP+BC (pretreated BC for 30 min before CDDP injection), CMN (200 mg/kg), and CDDP+CMN (pretreated CMN for 30 min before CDDP injection). These treatments were applied intraperitoneally for CDDP and with gavage for CMN and BC. The oxidative/antioxidant indicators, inflammatory cytokines, and histopathological alterations were examined. RESULTS: These alterations included a marked increase in malondialdehyde (MDA) level, significant decrease in catalase (CAT) and superoxide dismutase (SOD) activities, and significant elevation of tumor necrosis factor (TNF)-α, interleukin (IL)-1ß, interleukin (IL)-6 in the CDDP group compared with the other groups. Histopathologically, CDDP-induced severe myocardial degenerative changes were observed. However, the CDDP-induced disturbances in the above-mentioned parameters significantly improved by treatment with BC and particularly CMN. CONCLUSION: This study indicated that CDDP treatment markedly caused cardiotoxicity; however, treatment with CMN or BC ameliorated this cardiotoxicity in rats. Furthermore, these findings revealed that treatment with CMN has a higher cardioprotective effect than that with BC against CDDP-induced cardiotoxicity in rat cardiac tissues.
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Anzel Bahadır (2018) studied Cisplatin-induced cardiotoxicity (n=49). Curcumin and beta-carotene vs. Cisplatin alone was evaluated on Oxidative/antioxidant indicators, inflammatory cytokines, and histopathological alterations. Treatment with curcumin or beta-carotene ameliorated cisplatin-induced cardiotoxicity in rats, with curcumin demonstrating a higher cardioprotective effect than beta-carotene.
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