Key result
Thymoquinone limits cisplatin-induced myocardial injury in rats, driven by increased antiapoptotic Bcl-2 expression.
Why the study?
Cisplatin is cardiotoxic and the potential protective effect of thymoquinone against cisplatin-induced myocardial injury was investigated.
Does thymoquinone prevent cisplatin-induced myocardial injury in rats?
Does thymoquinone prevent cisplatin-induced myocardial injury in rats?
p-value: p=<0.05
Thymoquinone may offer a protective effect against cisplatin-induced cardiotoxicity by increasing antiapoptotic protein expression.
TQ may attenuate CP-induced myocardial injury in rats; leaves open clinical translation.
PURPOSE: T o investigate the possible protective effect of thymoquinone (TQ) in cisplatin (CP) induced myocardial injury. METHODS: A total of 28 adult male Wistar-Albino rats were randomly and equally divided into four groups as follows: Group 1 (control), Group 2 (CP at 15 mg/kg dose), Group 3 (TQ 40 mg/kg/day for two days prior to CP injection and on third day, CP at 15 mg/kg dose was intraperitoneally administered and TQ treatment continued until fifth day) and Group 4 (TQ at 40mg/kg/day dose for five days). RESULTS: There was a significant increment in CP group in terms of congestion, edema and pycnotic nuclei in myocardial fibers, comparing with other groups. TQ group exhibited significant increase in expression of antiapoptotic protein Bcl-2, comparing with CP group (p<0.05). In only CP administered group, expression of antiapoptotic protein Bcl-2 was lowest comparing with other groups. CONCLUSION: Established data indicate that cisplatin is cardiotoxic and thymoquinone may be useful in treating CP-induced cardiac injury.
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Adalı et al. (2016) studied Cisplatin-induced myocardial injury (n=28). Thymoquinone vs. Cisplatin alone was evaluated on Expression of antiapoptotic protein Bcl-2 and myocardial injury markers (p=<0.05). Thymoquinone significantly increased the expression of antiapoptotic protein Bcl-2 compared with cisplatin alone (p<0.05) and reduced myocardial congestion, edema, and pycnotic nuclei in rats.
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