High-affinity nicotinic acetylcholine receptor expression and trafficking abnormalities in psychiatric illness
- PMID: 23624811
- PMCID: PMC3766461
- DOI: 10.1007/s00213-013-3126-5
High-affinity nicotinic acetylcholine receptor expression and trafficking abnormalities in psychiatric illness
Abstract
Rationale: Nicotinic acetylcholine receptors (nAChRs) are a critical component of the cholinergic system of neurotransmission in the brain that modulates important physiological processes such as reward, cognition, and mood. Abnormalities in this system are accordingly implicated in multiple psychiatric illnesses, including addiction, schizophrenia, and mood disorders. There is significantly increased tobacco use, and therefore nicotine intake, in patient populations, and pharmacological agents that act on various nicotinic receptor subtypes ameliorate clinical features of these disorders. Better understanding of the molecular mechanisms underlying cholinergic dysfunction in psychiatric disease will permit more targeted design of novel therapeutic agents.
Results: The objective of this review is to describe the multiple cellular pathways through which chronic nicotine exposure regulates nAChR expression, and to juxtapose these mechanisms with evidence for altered expression of high-affinity nAChRs in human psychiatric illness. Here, we summarize multiple studies from pre-clinical animal models to human in vivo imaging and post-mortem experiments demonstrating changes in nAChR regulation and expression in psychiatric illness.
Conclusions: We conclude that a mechanistic explanation of nAChR abnormalities in psychiatric illness will arise from a fuller understanding of normal nAChR trafficking, along with the detailed study of human tissue, perhaps using novel biotechnological advances, such as induced pluripotent stem cells.
Conflict of interest statement
Similar articles
-
Nicotinic modulation of neuronal networks: from receptors to cognition.Psychopharmacology (Berl). 2006 Mar;184(3-4):292-305. doi: 10.1007/s00213-005-0070-z. Epub 2005 Jul 2. Psychopharmacology (Berl). 2006. PMID: 16001117 Review.
-
Organelle-specific single-molecule imaging of α4β2 nicotinic receptors reveals the effect of nicotine on receptor assembly and cell-surface trafficking.J Biol Chem. 2017 Dec 22;292(51):21159-21169. doi: 10.1074/jbc.M117.801431. Epub 2017 Oct 26. J Biol Chem. 2017. PMID: 29074617 Free PMC article.
-
Menthol Alone Upregulates Midbrain nAChRs, Alters nAChR Subtype Stoichiometry, Alters Dopamine Neuron Firing Frequency, and Prevents Nicotine Reward.J Neurosci. 2016 Mar 9;36(10):2957-74. doi: 10.1523/JNEUROSCI.4194-15.2016. J Neurosci. 2016. PMID: 26961950 Free PMC article.
-
Differential modulation of nicotinic acetylcholine receptor subtypes and synaptic transmission in chick sympathetic ganglia by PGE(2).J Neurophysiol. 2001 Jun;85(6):2498-508. doi: 10.1152/jn.2001.85.6.2498. J Neurophysiol. 2001. PMID: 11387396
-
Neuronal nicotinic receptors as brain targets for pharmacotherapy of drug addiction.CNS Neurol Disord Drug Targets. 2008 Nov;7(5):422-41. doi: 10.2174/187152708786927831. CNS Neurol Disord Drug Targets. 2008. PMID: 19128201 Review.
Cited by
-
Nicotinic receptors promote susceptibility to social stress in female mice linked with neuroadaptations within VTA dopamine neurons.Neuropsychopharmacology. 2022 Aug;47(9):1587-1596. doi: 10.1038/s41386-022-01314-4. Epub 2022 Apr 22. Neuropsychopharmacology. 2022. PMID: 35459925 Free PMC article.
-
Acute and chronic effects of clozapine on cholinergic transmission in cultured mouse superior cervical ganglion neurons.J Neurogenet. 2016 Sep-Dec;30(3-4):297-305. doi: 10.1080/01677063.2016.1229779. Epub 2016 Sep 14. J Neurogenet. 2016. PMID: 27627024 Free PMC article.
-
The Role of Muscarinic Receptors in the Pathophysiology of Mood Disorders: A Potential Novel Treatment?Curr Neuropharmacol. 2015;13(6):739-49. doi: 10.2174/1570159x13666150612230045. Curr Neuropharmacol. 2015. PMID: 26630954 Free PMC article. Review.
-
PET Imaging Estimates of Regional Acetylcholine Concentration Variation in Living Human Brain.Cereb Cortex. 2021 May 10;31(6):2787-2798. doi: 10.1093/cercor/bhaa387. Cereb Cortex. 2021. PMID: 33442731 Free PMC article.
-
Promoter IV-BDNF deficiency disturbs cholinergic gene expression of CHRNA5, CHRM2, and CHRM5: effects of drug and environmental treatments.J Neurochem. 2017 Oct;143(1):49-64. doi: 10.1111/jnc.14129. Epub 2017 Aug 16. J Neurochem. 2017. PMID: 28722769 Free PMC article.
References
-
- Benes FM. Nicotinic receptors and functional regulation of GABA cell microcircuitry in bipolar disorder and schizophrenia. Handb Exp Pharmacol. 2012:401–17. - PubMed
-
- Berton O, Nestler EJ. New approaches to antidepressant drug discovery: beyond monoamines. Nat Rev Neurosci. 2006;7:137–51. - PubMed
-
- Breese CR, Lee MJ, Adams CE, Sullivan B, Logel J, Gillen KM, Marks MJ, Collins AC, Leonard S. Abnormal regulation of high affinity nicotinic receptors in subjects with schizophrenia. Neuropsychopharmacology. 2000;23:351–64. - PubMed
-
- Breese CR, Marks MJ, Logel J, Adams CE, Sullivan B, Collins AC, Leonard S. Effect of smoking history on [3H]nicotine binding in human postmortem brain. J Pharmacol Exp Ther. 1997;282:7–13. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical