Please use this identifier to cite or link to this item: http://adhlui.com.ui.edu.ng/jspui/handle/123456789/2178
Title: The effect of modulation of glutathione levels on markers for Aflatoxin B,-induced cell damage
Authors: Farombi, E.O
Nwankwo, J.O
Emerole, G.O
Keywords: Glutathione S-transferase
Flatoxin B
Hepatotoxicity
Glutamyl transpeptidase
Glutathione
lipid peroxidation
Issue Date: 2005
Publisher: College of Medicine
Citation: Afr. J, Med. med. Sci. 2005: 34. 37-43
Abstract: The modulatory effect of glutathione levels on markers for aflatoxin B, (AFB,) -induced cell damage has been investigated in the rat (susceptible specie) and the (mouse resistant specie). The concentration of GSH was depleted and increased by administering paracetamol (PAM) and cysteine respectively and activities of glutathione S-transferase (GST) and y-glutamyl transpeptidase (y-GT) were determined. The effect of AFB, on hepatic lipid peroxidation in both species was also investigated. Treatment of rats with 2 mg/kg.bwt AFB, intraperitoneal^ caused a depletion of GSH in the liver to a minimum at 6 h (80% of the control value) and the level returned to normal after 24 h. GST was similarly increased to a maximum at 6 h and the level also returned to normal after 24 h. GSH and GST activities were not significantly affected in AFB,-treated mice. Orally administered PAM (400 mg/ kg.bwt) caused a depletion of GSH with a minimum at 6 h (59% and 36% of the control rats and mice respectively). Pretreatment of AFB, with PAM produced a serious depletion at 6 h (34% and 35% of the control rats and mice respectively). GST activities were also marginally increased in both animals. AFB, pretreatment mediated (P0.05) when cysteine was pretrcated alone with AFB,. Combined treatment of AFB, and PAM induced 177% increase in y-GT activity. Overall, our results suggest that the metabolism of aflatoxin B by GSH docs not lead to the formation of toxic products but rather GSH plays a protective role in AFB,-induced cell damage and GSH pathway is less utilised in mice.
URI: http://adhlui.com.ui.edu.ng/jspui/handle/123456789/2178
ISSN: 1116-4077
Appears in Collections:African Journal of Medicine and Medical Sciences

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