Effects of thymoquinone against cisplatin-induced cardiac injury in rats

被引:22
作者
Adali, Fahri [1 ]
Gonul, Yucel [1 ,2 ]
Kocak, Ahmet [1 ,3 ]
Yuksel, Yasemin [1 ,4 ]
Ozkececi, Gulay [1 ,5 ]
Ozdemir, Cigdem [1 ,6 ]
Tunay, Kamil [1 ,7 ]
Bozkurt, Mehmet Fatih [1 ,6 ]
Sen, Ozlem Gulec [1 ]
机构
[1] Afyon Kocatepe Univ, Fac Med, Dept Cardiovasc Surg, Afyon, Turkey
[2] Afyon Kocatepe Univ, Fac Med, Dept Anat, Afyon, Turkey
[3] Dumlupinar Univ, Fac Med, Dept Histol & Embryol, Kutahya, Turkey
[4] Zekai Tahir Burak Womens Hlth Educ & Res Hosp, Dept Embryol, Ankara, Turkey
[5] Afyon Kocatepe Univ, Dept Cardiol, Fac Med, Afyon, Turkey
[6] Afyon Kocatepe Univ, Dept Pathol, Fac Med, Afyon, Turkey
[7] Afyon Kocatepe Univ, Dept Emergency Med, Fac Med, Afyon, Turkey
关键词
Cisplatin; Cardiotoxicity; Genes; bcl-2; Rats; DOXORUBICIN-INDUCED CARDIOTOXICITY; INDUCED NEPHROTOXICITY; ANTITUMOR-ACTIVITY; NIGELLA-SATIVA; LUNG-CANCER; CELL-DEATH; CHEMOTHERAPY; GEMCITABINE; COMBINATION; EXPRESSION;
D O I
10.1590/S0102-865020160040000008
中图分类号
R61 [外科手术学];
学科分类号
摘要
PURPOSE: To 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.
引用
收藏
页码:271 / 277
页数:7
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