• DOI:10.1097/FBP.0b013e328337be54
• Corpus ID: 6609861

Inhibitory influence of mecamylamine on ethanol withdrawal-induced symptoms in C57BL/6J mice

@article{Bhutada2010InhibitoryIO,
  title={Inhibitory influence of mecamylamine on ethanol withdrawal-induced symptoms in C57BL/6J mice},
  author={Pravinkumar S. Bhutada and Yogita R. Mundhada and Kuldeep U Bansod and Sudhir N. Umathe and Vivek P. Kahale and Pankaj V. Dixit and Dharmendra R. Mundhada},
  journal={Behavioural Pharmacology},
  year={2010},
  volume={21},
  pages={90-95}
}

• P. Bhutada, Y. Mundhada, +4 authors D. Mundhada
• Published 1 March 2010
• Medicine, Chemistry
• Behavioural Pharmacology

Several reports show the involvement of neuronal nicotinic acetylcholine receptors (nAChRs) in the behavioral effects of ethanol, including ethanol drinking and relapse. Therefore, this study evaluated the effects of mecamylamine, a nAChR antagonist, on ethanol withdrawal signs. Ethanol dependence was induced in C57BL/6J mice by ethanol liquid diet administration. Animals were provided with nutritionally balanced control liquid diet (600 kcal/l) as their sole nutrient source on day 0; from days 1 to 4, 3% v/v of ethanol, followed by 6% v/v of ethanol (from days 5 to 7), and 10% v/v of ethanol (from days 8 to 10) were incorporated into the liquid diet. On day 11, ethanol liquid diet was replaced with nutritionally balanced control liquid diet, and ethanol withdrawal-induced physical signs were recorded. Results showed that acute administration of mecamylamine (1–4 mg/kg, intraperitoneally) dose-dependently attenuated ethanol withdrawal-induced signs, and these effects were comparable with those of diazepam (1–2 mg/kg, intraperitoneally). In addition, chronic administration of mecamylamine into ethanol diet-fed mice markedly attenuated the ethanol withdrawal sign scores, thus supporting the contention that nAChR is involved in ethanol dependence. In conclusion, our results suggest that mecamylamine exhibited inhibitory effects on ethanol withdrawal signs which could be mediated through nAChR.