Self-administration of 5-iodo-A-85380, a beta2-selective nicotinic receptor ligand, by operantly trained rats
- PMID: 12960773
- DOI: 10.1097/00001756-200308060-00020
Self-administration of 5-iodo-A-85380, a beta2-selective nicotinic receptor ligand, by operantly trained rats
Abstract
It is widely accepted that nicotine is the active ingredient of tobacco smoke that promotes tobacco dependence. Nicotine interacts with several subtypes of nicotinic acetylcholine receptors (nAChRs). In brain, it primarily targets nAChRs that contain beta2 and alpha4 subunits in combination and those composed of solely alpha7 subunits. The present study tested whether operantly trained rats would self-administer a ligand active at beta2-containing (i.e. not alpha7) nAChRs. Male Sprague-Dawley rats were trained to lever press for i.v. cocaine self-administration. After 2 weeks of cocaine washout, rats were given operant access to 5-iodo-A-85380 (5IA), a beta2-selective nAChR ligand, in daily 1 h sessions. The rats rapidly developed a stable level of 5IA self-administration behavior (unit dose = 5 nmol/kg/infusion). This finding suggests that interaction with beta2-containing nAChRs, without direct involvement of alpha7 receptors, can produce reinforcement and thereby can support self-administration behavior.
Similar articles
-
Ligands selective for alpha4beta2 but not alpha3beta4 or alpha7 nicotinic receptors generalise to the nicotine discriminative stimulus in the rat.Psychopharmacology (Berl). 2007 Feb;190(2):157-70. doi: 10.1007/s00213-006-0596-8. Epub 2006 Nov 18. Psychopharmacology (Berl). 2007. PMID: 17115136
-
Crucial role of alpha4 and alpha6 nicotinic acetylcholine receptor subunits from ventral tegmental area in systemic nicotine self-administration.J Neurosci. 2008 Nov 19;28(47):12318-27. doi: 10.1523/JNEUROSCI.3918-08.2008. J Neurosci. 2008. PMID: 19020025 Free PMC article.
-
Attenuation of nicotine taking and seeking in rats by the stoichiometry-selective alpha4beta2 nicotinic acetylcholine receptor positive allosteric modulator NS9283.Psychopharmacology (Berl). 2017 Feb;234(3):475-484. doi: 10.1007/s00213-016-4475-7. Epub 2016 Nov 14. Psychopharmacology (Berl). 2017. PMID: 27844094
-
Positive allosteric modulation of α4β2 nicotinic acetylcholine receptors as a new approach to smoking reduction: evidence from a rat model of nicotine self-administration.Psychopharmacology (Berl). 2013 Nov;230(2):203-13. doi: 10.1007/s00213-013-3145-2. Epub 2013 May 28. Psychopharmacology (Berl). 2013. PMID: 23712602 Free PMC article.
-
Alpha7 nicotinic acetylcholine receptors modulate motivation to self-administer nicotine: implications for smoking and schizophrenia.Neuropsychopharmacology. 2012 Apr;37(5):1134-43. doi: 10.1038/npp.2011.299. Epub 2011 Dec 14. Neuropsychopharmacology. 2012. PMID: 22169946 Free PMC article.
Cited by
-
Quantitative Molecular Imaging of Neuronal Nicotinic Acetylcholine Receptors in the Human Brain with A-85380 Radiotracers.Curr Med Imaging Rev. 2011 May 1;7(2):107-112. doi: 10.2174/157340511795445676. Curr Med Imaging Rev. 2011. PMID: 22773924 Free PMC article.
-
Effects of nicotinic acetylcholine receptor agonists in assays of acute pain-stimulated and pain-depressed behaviors in rats.J Pharmacol Exp Ther. 2015 Nov;355(2):341-50. doi: 10.1124/jpet.115.226803. J Pharmacol Exp Ther. 2015. PMID: 26359313 Free PMC article.
-
Neurobiological Mechanisms of Nicotine Reward and Aversion.Pharmacol Rev. 2022 Jan;74(1):271-310. doi: 10.1124/pharmrev.121.000299. Pharmacol Rev. 2022. PMID: 35017179 Free PMC article. Review.
-
Denicotinized versus average nicotine tobacco cigarette smoking differentially releases striatal dopamine.Nicotine Tob Res. 2013 Jan;15(1):11-21. doi: 10.1093/ntr/nts029. Epub 2012 Apr 5. Nicotine Tob Res. 2013. PMID: 22491891 Free PMC article.
-
Pharmacological characterization of 5-iodo-A-85380, a β2-selective nicotinic receptor agonist, in mice.J Psychopharmacol. 2022 Nov;36(11):1280-1293. doi: 10.1177/02698811221132214. Epub 2022 Nov 2. J Psychopharmacol. 2022. PMID: 36321267 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources