α6-containing nicotinic acetylcholine receptors (nAChRs) show a restricted expression pattern in the brain.
Neural nicotinic acetylcholine receptors containing α6 subunits are expressed on dopamine-releasing neurons in the midbrain.[6][7]
Function
These receptors play a key role in regulating dopaminergic neurotransmission.
Dopamine release following activation of these neurons is thought to be involved in the addictive properties of nicotine.[8][9][10]
In addition to nicotine, research in animals has implicated α6-containing nAChRs in the abusive and addictive properties of ethanol, with mecamylamine demonstrating a potent ability to block these properties.
Clinical significance
Because of their selective distribution and role in dopamine regulation, α6-containing receptors have been investigated as therapeutic targets.
Due to their selective localisation on dopaminergic neurons, α6-containing nACh receptors have also been suggested as a possible therapeutic target for the treatment of Parkinson's disease.[11][12]
Interactive pathway map
Click on genes, proteins and metabolites below to link to respective articles.[§ 1]
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|alt=Nicotine Activity on Dopaminergic Neurons edit]]
^Le Novère N, Zoli M, Changeux JP (November 1996). "Neuronal nicotinic receptor alpha 6 subunit mRNA is selectively concentrated in catecholaminergic nuclei of the rat brain". The European Journal of Neuroscience. 8 (11): 2428–2439. doi:10.1111/j.1460-9568.1996.tb01206.x. PMID8950106. S2CID23102912.
^Quik M, McIntosh JM (February 2006). "Striatal alpha6* nicotinic acetylcholine receptors: potential targets for Parkinson's disease therapy". The Journal of Pharmacology and Experimental Therapeutics. 316 (2): 481–489. doi:10.1124/jpet.105.094375. PMID16210393. S2CID20050682.
^Bordia T, Grady SR, McIntosh JM, Quik M (July 2007). "Nigrostriatal damage preferentially decreases a subpopulation of alpha6beta2* nAChRs in mouse, monkey, and Parkinson's disease striatum". Molecular Pharmacology. 72 (1): 52–61. doi:10.1124/mol.107.035998. PMID17409284. S2CID25281990.
Keiger CJ, Case LD, Kendal-Reed M, Jones KR, Drake AF, Walker JC (January 2003). "Nicotinic cholinergic receptor expression in the human nasal mucosa". The Annals of Otology, Rhinology, and Laryngology. 112 (1): 77–84. doi:10.1177/000348940311200115. PMID12537063. S2CID24705718.
Ebihara M, Ohba H, Ohno SI, Yoshikawa T (September 2002). "Genomic organization and promoter analysis of the human nicotinic acetylcholine receptor alpha6 subunit (CHNRA6) gene: Alu and other elements direct transcriptional repression". Gene. 298 (1): 101–108. doi:10.1016/S0378-1119(02)00925-3. PMID12406580.
Graham A, Court JA, Martin-Ruiz CM, Jaros E, Perry R, Volsen SG, et al. (2002). "Immunohistochemical localisation of nicotinic acetylcholine receptor subunits in human cerebellum". Neuroscience. 113 (3): 493–507. doi:10.1016/S0306-4522(02)00223-3. PMID12150770. S2CID39839166.
Elliott KJ, Ellis SB, Berckhan KJ, Urrutia A, Chavez-Noriega LE, Johnson EC, et al. (1997). "Comparative structure of human neuronal alpha 2-alpha 7 and beta 2-beta 4 nicotinic acetylcholine receptor subunits and functional expression of the alpha 2, alpha 3, alpha 4, alpha 7, beta 2, and beta 4 subunits". Journal of Molecular Neuroscience. 7 (3): 217–228. doi:10.1007/BF02736842. PMID8906617. S2CID45737923.