Nicotinic receptors in non-human primates: Analysis of genetic and functional conservation with humans. (September 2015)

• Record Type: Journal Article
• Authors: Shorey-Kendrick, Lyndsey E.; Ford, Matthew M.; Allen, Daicia C.; Kuryatov, Alexander; Lindstrom, Jon; Wilhelm, Larry; Grant, Kathleen A.; Spindel, Eliot R.
• Is Part Of: Neuropharmacology. Volume 96:Part B(2015)
• Page Start: 263
• Page End: 273
• Publication Date: 2015-09
• Subjects: Nicotinic receptor -- Nicotine -- Non-human primate -- Rhesus -- Cynomolgus -- Macaque; α-CTx α-conotoxin -- GWAS genome wide association study -- NHP non-human primate -- nAChR nicotinic acetylcholine receptor -- SNP single nucleotide polymorphism; Neuropsychopharmacology -- Periodicals; Autonomic Agents -- Periodicals; Neuropsychopharmacologie -- Périodiques; Neuropsychopharmacology; Periodicals; Electronic journals; 615.78
• DOI: 10.1016/j.neuropharm.2015.01.023
• Languages: English
• ISSNs: 0028-3908

Abstract

Abstract: Nicotinic acetylcholine receptors (nAChRs) are highly conserved between humans and non-human primates. Conservation exists at the level of genomic structure, protein structure and epigenetics. Overall homology of nAChRs at the protein level is 98% in macaques versus 89% in mice, which is highly relevant for evaluating subtype-specific ligands that have different affinities in humans versus rodents. In addition to conservation at the protein level, there is high conservation of genomic structure in terms of intron and exon size and placement of CpG sites that play a key role in epigenetic regulation. Analysis of single nucleotide polymorphisms (SNPs) shows that while the majority of SNPs are not conserved between humans and macaques, some functional polymorphisms are. Most significantly, cynomolgus monkeys express a similar α5 nAChR Asp398Asn polymorphism to the human α5 Asp398Asn polymorphism that has been linked to greater nicotine addiction and smoking related disease. Monkeys can be trained to readily self-administer nicotine, and in an initial study we have demonstrated that cynomolgus monkeys bearing the α5 D398N polymorphism show a reduced behavioral sensitivity to oral nicotine and tend to consume it in a different pattern when compared to wild-type monkeys. Thus the combination of highly homologous nAChR, higher cortical functions and capacity for complex training makes non-human primates a unique model to study in vivo functions of nicotinic receptors. In particular, primate studies on nicotine addiction and evaluation of therapies to prevent or overcome nicotine addiction are likely to be highly predictive of treatment outcomes in humans. This article is part of the Special Issue entitled 'The Nicotinic Acetylcholine Receptor: From Molecular Biology to Cognition'. Highlights: Genomic structure of macaque nAChRs are compared to human. Non-human primate nAChR coding sequences are compared to human. Cynomolgus monkeys are shown to express an α5 Asp398Asn polymorphism like humans. Monkeys can be trained to self-administer nicotine in multiple paradigms. The α5 Asp398Asn polymorphism affects nicotine self-administration in monkeys.