Journal
EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 858, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.ejphar.2019.172467
Keywords
Doxorubicin; Acute cardiotoxicity; Inflammation; DNA damage and apoptosis; beta-Caryophyllene; Cardioprotection
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Funding
- United Arab Emirates University, United Arab Emirates [SURE plus, CMHS research, University Program for Advanced Research, and Center-Based Interdisciplinary grants]
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The present study investigates the cardioprotective effect of beta-caryophyllene against doxorubicin-induced acute cardiotoxicity in rats. Doxorubicin (12.5 mg/kg) and beta-caryophyllene (25, 50 or 100 mg/kg) were administered intraperitoneally to male albino Wistar rats. Doxorubicin-treated rats showed elevated levels of creatine kinase-MB in serum and oxidative stress in the myocardium as evidenced by decreased superoxide dismutase, catalase and glutathione with a concomitant rise in malondialdehyde levels. Doxorubicin also induced pro-inflammatory cytokines release following activation of the nuclear factor kappa-B and elevated expressions of inducible nitric oxide synthase and cyclooxygenase-2 in the myocardium. Additionally, doxorubicin also increased expression of gamma-H2AX, a marker of DNA damage as well as increased expression of proapoptotic (Bax, p53, and active caspase-3) proteins along with the decreased expression of anti-apoptotic protein, Bcl2 in the myocardium. The histological and ultrastructural studies further revealed edema, inflammation and structural degeneration of cardiomyocytes following doxorubicin injection. However, treatment with beta-caryophyllene showed significant cardioprotective effects as evidenced by favorable improvement of biochemical and molecular parameters along with remarkable preservation of cardiomyocytes in histological and ultrastructural studies. Results of the present study demonstrate that beta-caryophyllene has potential to protect heart against doxorubicin-induced acute cardiotoxicity in rats. Moreover, the antioxidant and free radical scavenging properties of beta-caryophyllene was confirmed by in vitro assays. Provided the anticancer and chemosensitizing properties of beta-caryophyllene, the cardioprotective effects of beta-caryophyllene are suggestive of its multiple properties that provides an additional basis of its possible therapeutic application in chemotherapy-associated cardiotoxicity.
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