| First Author | Besson M | Year | 2016 |
| Journal | Psychopharmacology (Berl) | Volume | 233 |
| Issue | 18 | Pages | 3297-314 |
| PubMed ID | 27385416 | Mgi Jnum | J:315589 |
| Mgi Id | MGI:6829323 | Doi | 10.1007/s00213-016-4362-2 |
| Citation | Besson M, et al. (2016) Alterations in alpha5* nicotinic acetylcholine receptors result in midbrain- and hippocampus-dependent behavioural and neural impairments. Psychopharmacology (Berl) 233(18):3297-314 |
| abstractText | RATIONALE: Evidence links alterations in alpha5-containing nicotinic receptors (alpha5*-nAChRs) to nicotine addiction. Notably, the rs16969968 polymorphism in the alpha5 gene (alpha5SNP) increases the risk for heavy smoking and impairs nicotine-rewarding properties in mice. Additional work is needed to understand how native and polymorphic alpha5*-nAChRs contribute to processes associated with the risk for nicotine addiction. OBJECTIVES: We aimed at understanding the contribution of alpha5*-nAChRs to endophenotypes like increased responses to novelty and anxiety, known to promote vulnerability to addiction, and to the response of the dopamine and serotonin systems to nicotine. METHODS: Behavioural phenotypes were investigated in mice lacking the alpha5 gene (alpha5(-/-)). Nicotine injections were performed to test the consequences of nicotine exposure on the phenotypes identified. Dopamine and serotonin signalling were assessed using in vivo microdialysis and electrophysiology. We used lentiviral vectors to compare the consequences of re-expressing either the alpha5 wild-type allele or the alpha5SNP in specific brain areas of alpha5(-/-) mice. RESULTS: alpha5(-/-) mice did not exhibit high responses to novelty but showed decreased novelty-induced rearing behaviour together with high anxiety. Exposure to high doses of nicotine rescued these phenotypes. We identified altered spontaneous and nicotine-elicited serotonin and dopamine activity in alpha5(-/-) mice. Re-expression of alpha5 in the ventral tegmental area and hippocampus rescued rearing and anxiety levels in alpha5(-/-) mice, respectively. When expressing the alpha5SNP instead, this resulted in a knockout-like phenotype for both behaviours. CONCLUSIONS: We propose that altered alpha5*-nAChR cholinergic signalling contributes to emotional/behavioural impairments that may be alleviated by nicotine consumption. |
