TY - JOUR
T1 - Ethanol and nicotine interaction on liver oxidative status
T2 - An experimental study
AU - Bölükbaş, Füsun Filiz
AU - Bölükbaş, Cengiz
AU - Kabasakal, Levent
AU - Horoz, Mehmet
AU - Sonsuz, Abdullah
AU - Uysal, Meral Keyer
AU - Övünç, Oya
PY - 2009
Y1 - 2009
N2 - Objective: To investigate the additive effect of ethanol and nicotine on rat liver oxidative status following either alone or combined sub-chronic administration. Material and Methods: Forty-eight female Sprague Dewley rats were grouped randomly into one of the protocols, which consisted of treatment for 10 days with ethanol 2 g/kg/day (ethanol group, n= 12), nicotine 0.15 mg/kg/day (nicotine group, n= 12), both drugs (ethanol plus nicotine group, n= 12) or saline solution (control group, n= 10) for 10 days. Following 10 days of administration of thesethe above-mentioned agents, malondialdehyde concentration, reduced glutathione concentration and glutathione peroxidase activity were assessed in the liver. Results: The ethanol plus nicotine group had significantly higher malondialdehyde and lower glutathione concentrations than either the ethanol and nicotine and the control groups (both, p< 0.05). The ethanol or nicotine group had significantly higher malondialdehyde concentration and lower glutathione concentration and glutathione peroxidase activity than the control group (all p< 0.05). Malondialdehyde and glutathione concentration was not significantly higher in the ethanol group than in the nicotine group (both, p> 0.05). No significant difference was observed in glutathione peroxidase activity of ethanol, nicotine or ethanol plus nicotine groups (all p> 0.05). Conclusions: Co-administration of ethanol and nicotine results with significant increase in lipid peroxidation and significant decrease in glutathionelevels compared to their separate administration.
AB - Objective: To investigate the additive effect of ethanol and nicotine on rat liver oxidative status following either alone or combined sub-chronic administration. Material and Methods: Forty-eight female Sprague Dewley rats were grouped randomly into one of the protocols, which consisted of treatment for 10 days with ethanol 2 g/kg/day (ethanol group, n= 12), nicotine 0.15 mg/kg/day (nicotine group, n= 12), both drugs (ethanol plus nicotine group, n= 12) or saline solution (control group, n= 10) for 10 days. Following 10 days of administration of thesethe above-mentioned agents, malondialdehyde concentration, reduced glutathione concentration and glutathione peroxidase activity were assessed in the liver. Results: The ethanol plus nicotine group had significantly higher malondialdehyde and lower glutathione concentrations than either the ethanol and nicotine and the control groups (both, p< 0.05). The ethanol or nicotine group had significantly higher malondialdehyde concentration and lower glutathione concentration and glutathione peroxidase activity than the control group (all p< 0.05). Malondialdehyde and glutathione concentration was not significantly higher in the ethanol group than in the nicotine group (both, p> 0.05). No significant difference was observed in glutathione peroxidase activity of ethanol, nicotine or ethanol plus nicotine groups (all p> 0.05). Conclusions: Co-administration of ethanol and nicotine results with significant increase in lipid peroxidation and significant decrease in glutathionelevels compared to their separate administration.
KW - Alcohols
KW - Nicotine
KW - Oxidative stress
UR - http://www.scopus.com/inward/record.url?scp=74049105526&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:74049105526
SN - 1300-0292
VL - 29
SP - 932
EP - 937
JO - Turkiye Klinikleri Journal of Medical Sciences
JF - Turkiye Klinikleri Journal of Medical Sciences
IS - 4
ER -