机构地区:[1]Department of Biochemistry and Molecular Biology,Rajshahi University [2]Applied Chemistry and Chemical Technology,Rajshahi University
出 处:《Asian Pacific Journal of Tropical Biomedicine》2013年第2期105-110,共6页亚太热带生物医学杂志(英文版)
基 金:supported by the Ministry of National Science,Information and Comunication Technology(NSICT)of People's Republic of Bangladesh with Grant No.(89)NST/Biology/07-2011
摘 要:Objective:To determine the hepatoprotective effect of acetone semicarbazone(ASC)in vivo in normal and Ehrlich ascites carcinoma(EAC)bearing male Swiss albino mice.Methods:Druginduced changes in biochemical and behavioral parameters at dose of 2.0 mg/kg body weight for14 d and nullifying the toxicity induced by EAC cells were studied.The histopathology studies of the protective effects of ASC on vital organs were also assessed.Results:The administration of ASC made insignificant changes in body weight and behavioral(salivation,diarrhea,muscular numbness)changes during treatment period due to minor toxicity were minimized after the treatment in normal mice.The biochemical parameters,including serum glutamate pyruvate transaminase,glutamate oxaloactate transaminase,alkaline phosphatase,serum glucose,cholesterol,urea,triglyceride and billirubin changed modestly in normal mice receiving ASC.Though the treatment continued,these values gradually decreased to normal level after the treatment.In EAC bearing mice,the toxic effects due to EAC cells in all cases were nullified by treatment with the ASC.Significant abnormalities were not detected in histology of the various organs of the normal mice treated with ASC.Conclusions:ASC can,therefore,be considered safe in formulating novel anticancer drug,as it exhibits strong protective effect against EAC cell bearing mice.Objective:To determine the hepatoprotective effect of acetone semicarbazone(ASC)in vivo in normal and Ehrlich ascites carcinoma(EAC)bearing male Swiss albino mice.Methods:Druginduced changes in biochemical and behavioral parameters at dose of 2.0 mg/kg body weight for14 d and nullifying the toxicity induced by EAC cells were studied.The histopathology studies of the protective effects of ASC on vital organs were also assessed.Results:The administration of ASC made insignificant changes in body weight and behavioral(salivation,diarrhea,muscular numbness)changes during treatment period due to minor toxicity were minimized after the treatment in normal mice.The biochemical parameters,including serum glutamate pyruvate transaminase,glutamate oxaloactate transaminase,alkaline phosphatase,serum glucose,cholesterol,urea,triglyceride and billirubin changed modestly in normal mice receiving ASC.Though the treatment continued,these values gradually decreased to normal level after the treatment.In EAC bearing mice,the toxic effects due to EAC cells in all cases were nullified by treatment with the ASC.Significant abnormalities were not detected in histology of the various organs of the normal mice treated with ASC.Conclusions:ASC can,therefore,be considered safe in formulating novel anticancer drug,as it exhibits strong protective effect against EAC cell bearing mice.
关 键 词:EAC cell Host TOXICITY ACETONE SEMICARBAZONE SCHIFF bases Histopathology SUBACUTE TOXICITY
分 类 号:R114[医药卫生—卫生毒理学]
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