Tarique Mahmood1 ,
Hefazat H Siddiqui1,
Rakesh Dixit2,
Paramdeep Bagga1,
Md. Sarfaraj Hussain1
1Faculty of Pharmacy, Integral University, Dasauli, Kursi Road, Lucknow-226026;
2Department of Pharmacology, King George Medical University, Lucknow-226018, Uttar Pradesh, India.
For correspondence:- Tarique Mahmood
Email: ansaritariq79@yahoo.co.in Tel:+91-9918681701
Received: 27 March 2014
Revised: 21 November 2014
Published: 30 January 2015
Citation:
Mahmood T, Siddiqui HH, Dixit R, Bagga P, Hussain M.
Protective effect of Bombyx mori L Cocoon (Abresham) and its formulations against isoproterenol-induced cardiac damage. Trop J Pharm Res 2015; 14(1):63-72
doi:
10.4314/tjpr.v14i1.10
© 2015 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..
Abstract
Purpose:To investigate the potential activity of Bombyx mori and its formulations against isoproterenol (ISO) induced cardiotoxicity.
Methods:Wistar rats were orally pretreated with the ethanol extract of Bombyx mori cocoons in two doses (250 and 500 mg/kg) for 30 days; rats were similarly pretreated with its polyherbal formulations incorporating Khamira Abresham sada (KAS) and Khamira Abresham Hakim Arshadwala (KAHAW) (800 mg/kg), standard drug metoprolol (10 mg/kg) and normal saline for 30 days. Cardiotoxicity was induced by administration of isoproterenol (ISO, 85 mg/kg, subcutaneous) given twice on days 29 and 30 in all six pre-treated groups (n = 6) except the normal control. Cardiotoxicity was assessed by morphological and biochemical evaluation and further confirmed by histopathological studies.
Results:Pretreatment with Bombyx mori (500 mg/kg), KAHAW and KAS significantly decreased (p < 0.01) the heart weight:body weight (HW:BW) ratio; significantly decreases the elevated activities of the cardiac marker enzymes, namely, asparate transaminase (AST) (p < 0.01), alanine transaminase (ALT) (p < 0.01), lactate dehydrogenase (LDH) (p < 0.01) ,creatinine kinase (CK-MB) (p < 0.01) and thiobarbituric acid reactive substances (TBARS) (p < 0.01) similar to the standard drug metoprolol (p < 0.01) in ISO-injected rats. Pre-treatment of rats with Bombyx mori (500 mg/kg), KAS, KAHAW and metoprolol challenged with ISO also showed absence of troponin. Pretreatment with B. mori (500 mg/kg), KAHAW and KAS significantly increased the activities of Superoxide dismutase (SOD) (p < 0.01), Tissue glutathione (GSH) (p < 0.01) and catalase (p < 0.01) similar to the standard drug metoprolol (p < 0.01).
Conclusion:The findings of this study indicate that Bombyx mori as well as its polyherbal formulations exerts potent cardioprotection against isoproterenol-induced cardiotoxicity. This effect is comparable with that of metoprolol.
Keywords: Bombyx mori, Myocardial necrosis, Oxidative stress, Cardiotoxicity, Khamira Abresham, Metoprolol, Isoproterenol