Nigella sativa protects against isoproterenol-induced myocardial infarction by alleviating oxidative stress, biochemical alterations and histological damage
10.1016/j.apjtb.2016.12.020
- Author:
Md. Quamrul HASSAN
1
;
Mohd. AKHTAR
1
;
Abul Kalam NAJMI
1
;
Sayeed AHMED
2
;
Aftab AHMAD
3
Author Information
1. Department of Pharmacology, Faculty of Pharmacy, Jamia Hamdard (Hamdard University)
2. Department of Pharmacognosy, Faculty of Pharmacy, Jamia Hamdard (Hamdard University)
3. Health Information Technology Department, Jeddah Community College, King Abdulaziz University
- Publication Type:Journal Article
- Keywords:
Antioxidant;
Isoproterenol;
Myocardial necrosis;
Nigella sativa;
Oxidative stress
- From:Asian Pacific Journal of Tropical Biomedicine
2017;7(4):294-299
- CountryChina
- Language:Chinese
-
Abstract:
Objective To evaluate the cardioprotective effect of Nigella sativa L. (N. sativa) in isoproterenol-induced myocardial infarction (MI). Methods Groups were treated with different doses of ethanol extract of N. sativa (EENS) and N. sativa oil alone and along with enalapril for 28 days. MI was induced by subcutaneous administration of isoproterenol (85 mg/kg) in two consecutive doses. Levels of cardiac biomarkers and antioxidant enzymes such as creatine kinase–N-acetyl-L-cysteine, lactate dehydrogenase, aspartate aminotransferase, malondialdehyde, superoxide dismutase, reduced glutathione and catalase were evaluated along with gross histopathological examination. Results Isoproterenol (85 mg/kg) induced MI by causing the significant (P < 0.01) reduction in the activity of cardiac biomarkers (creatine kinase–N-acetyl-L-cysteine, lactate dehydrogenase, aspartate aminotransferase) and antioxidant markers (superoxide dismutase, catalase, glutathione) along with significant (P < 0.01) increase in the level of malondialdehyde. Furthermore, histopathological evaluation also confirmed the isoproterenol-induced MI. Pretreatment with EENS (800 mg/kg) and combination of EENS (800 mg/kg) with enalapril (1 mg/kg) significantly (P < 0.01) prevented the development of these alteration and restored activity of cardiac biomarkers as well as antioxidant markers almost near to normal levels. Histopathological evaluation of cardiac tissue further confirmed the restoration of biochemical activity. Conclusions Experimental findings thus indicate that EENS (800 mg/kg) demonstrated cardioprotective effect against isoproterenol-induced MI by restoring cardiac biomarkers and antioxidant status.
