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Wiley InterScience | ||||||||||||
![]() Genes, Brain and BehaviorVolume 6 Issue 8, Pages 728 - 735 Published Online: 2 Feb 2007 Journal compilation © 2010 Blackwell Publishing Ltd/International Behavioural and Neural Genetics Society Published jointly with the International Behavioural and Neural Genetics Society (IBANGS)
Abstract | References | Full Text: HTML, PDF (Size: 622K) | Related Articles | Citation Tracking Downregulation of mu opioid receptor by RNA interference in the ventral tegmental area reduces ethanol consumption in mice Copyright Journal compilation © 2007 Blackwell Publishing Ltd KEYWORDS Ethanol consumption • lentivirus • opioid receptor • RNA interference • ventral tegmental area ABSTRACTPharmacological and genetic studies have implicated the mu opioid receptor (MOR) in the regulation of ethanol intake in animal models and humans. Non-specific antagonists of opioid receptors have been shown to affect ethanol consumption when infused directly into the ventral tegmental area (VTA) of rats. However, administration of MOR-selective antagonists into the VTA has yielded mixed results. We used RNA interference (RNAi) to specifically decrease levels of MOR messenger RNA in the VTA of mice and examined the effect on ethanol consumption in a two-bottle choice paradigm. Mice were injected in the VTA with lentivirus expressing either a small hairpin RNA (shRNA) targeting MOR or a control shRNA. One week after virus injection, mice were examined for ethanol consumption in a two-bottle choice experiment with increasing concentrations of ethanol over the course of 1 month. Expression of an shRNA targeting MOR in the VTA led to a significant reduction in ethanol consumption. These results strengthen the hypothesis that MOR in the VTA is one of the key brain substrates mediating alcohol consumption. The RNAi combined with lentiviral delivery can be used successfully in brain to effect a sustained reduction in expression of specific genes for behavioral analysis. Received 17 October 2006, revised 20 December 2006, accepted for publication 2 January 2007 |
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