Please use this identifier to cite or link to this item: http://localhost:80/xmlui/handle/123456789/15095
Title: Efficacy of herbal coded Hepcon on drug induced hepatitis in experimental animals through histopathological and biochemical analysis
Authors: Jamil, Muhammad Saim
Mahmood, Zahid
Saeed, Aftab
Jamil, Amir
Usmanghani, Khan
Asif, Hafiz Muhammad
Hassan, Sajjad-al
Roohi, Mahira
Keywords: Drug induced hepatitis
efficacy
Hepcon
experimental animals
Issue Date: 21-Sep-2013
Publisher: Karachi: Faculty of Pharmacy, University of Karachi
Citation: Saim Jamil, M., Mahmood, Z., Saeed, A., Jamil, A., Usmanghani, K., Muhammad Asif, H., & Roohi, M. (2013). Efficacy of herbal coded Hepcon on drug induced hepatitis in experimental animals through histopathological and biochemical analysis. Pakistan Journal of Pharmaceutical Sciences, 26(5).
Abstract: Drug-induced liver injury is the leading cause for more than 50 percent of cases of acute liver failure. This study was conducted on herbo-mineral formulation “Hepcon” to evaluate its hepatoprotective effects in drug induced hepatitis in experimental animals. The liver injury was introduced with over dosage of non steroidal anti-inflammatory drugs (NSAIDs) and carbon tetrachloride (CCl4). The herbo-mineral formulations “Hepcon” consist of Zingiber officinale, Piprum nigrum, Ammonium chloride and Arsenic trioxide (Hartal warqi). The aqueous extraction was administered to experimental animals. Thereafter their LFTs, IgG, and tissue pathology was studied. It was observed on the basis of biochemical and histopathological analysis that animals which were subjected to Hepcon became normal in 60 days whereas those as control group did not showed improvements and most of them died. It was concluded that the efficacy of Hepcon to treat liver injury caused by CCl4 and NSAIDs is very effective, and no side effects were noticed.
URI: http://142.54.178.187:9060/xmlui/handle/123456789/15095
ISSN: 1011-601X
Appears in Collections:2006,Part-1

Files in This Item:
File Description SizeFormat 
Paper-21.htm132 BHTMLView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.