Cardioprotective effect of cannabidiol in rats exposed to doxorubicin toxicity

被引:86
作者
Fouad, Amr A. [1 ]
Albuali, Waleed H. [2 ]
Al-Mulhim, Abdulruhman S. [3 ]
Jresat, Iyad [4 ]
机构
[1] King Faisal Univ, Dept Biomed Sci, Div Pharmacol, Coll Med, Al Hasa 31982, Saudi Arabia
[2] King Faisal Univ, Dept Pediat, Coll Med, Al Hasa 31982, Saudi Arabia
[3] King Faisal Univ, Dept Surg, Coll Med, Al Hasa 31982, Saudi Arabia
[4] King Faisal Univ, Dept Biomed Sci, Coll Med, Div Pathol, Al Hasa 31982, Saudi Arabia
关键词
Cannabidiol; Doxorubicin cardiotoxicity; Oxidative stress; Inflammation; Rats; INDUCED CARDIOTOXICITY; NITRIC-OXIDE; OXIDATIVE STRESS; NUCLEAR-FACTOR; KAPPA-B; SURVIVIN; APOPTOSIS; INHIBITION; INFLAMMATION; CONSTITUENT;
D O I
10.1016/j.etap.2013.04.018
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The potential protective effect of cannabidiol, the major non-psychotropic Cannabis constituent, was investigated against doxorubicin cardiotoxicity in rats. Cardiotoxicity was induced by six equal doses of doxorubicin (2.5 mg kg(-1) i.p., each) given at 48h intervals over two weeks to achieve a total dose of 15 mg kg(-1). Cannabidiol treatment (5 mg kg(-1)/day, i.p.) was started on the same day of doxorubicin administration and continued for four weeks. Cannabidiol significantly reduced the elevations of serum creatine kinase-MB and troponin T, and cardiac malondialdehyde, tumor necrosis factor-alpha, nitric oxide and calcium ion levels, and attenuated the decreases in cardiac reduced glutathione, selenium and zinc ions. Histopathological examination showed that cannabidiol ameliorated doxorubicin-induced cardiac injury. Immunohistochemical analysis revealed that cannabidiol significantly reduced the expression of inducible nitric oxide synthase, nuclear factor-kappa B, Fas ligand and caspase-3, and increased the expression of survivin in cardiac tissue of doxorubicin-treated rats. These results indicate that cannabidiol represents a potential. protective agent against doxorubicin cardiac injury. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:347 / 357
页数:11
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