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Hippocampal ?4ß2 nicotinic acetylcholine receptor involvement in the enhancing effect of acute nicotine on contextual fear conditioning

Hippocampal ?4ß2 nicotinic acetylcholine receptor involvement in the enhancing effect of acute nicotine on contextual fear conditioning
Hippocampal ?4ß2 nicotinic acetylcholine receptor involvement in the enhancing effect of acute nicotine on contextual fear conditioning
Nicotine is known to enhance learning and memory in hippocampus-dependent tasks such as contextual fear conditioning. The present study was designed to directly examine whether the hippocampus plays a role in mediating this enhancement and which nicotinic acetylcholine receptor (nAChR) subtypes localized to the hippocampus are critical for enhanced learning. Contextual fear conditioning consisted of two white noise conditioned stimuli presentations, each coterminating with a 2 s, 0.57 mA footshock separated by a 120 s intertrial interval. Nicotine (0.09, 0.18, and 0.35 microg per side) was bilaterally infused into the dorsal hippocampus before training and testing. Infusions of nicotine into the dorsal hippocampus produced a dose-dependent enhancement of contextual fear conditioning. To determine which nAChRs are critical to the enhancing effect of nicotine, the preferential ?4ß2 nAChR antagonist, dihydro-beta-erythroidine (DHbetaE) (6.00 and 18.00 microg per side), or the preferential ?7 nAChR antagonist, methyllycaconitine (MLA) (13.50 and 27.00 microg per side), was bilaterally infused into the dorsal hippocampus before systemic injections of nicotine (0.09 mg/kg). DHßE infusions dose-dependently blocked the enhancement of contextual fear conditioning by nicotine, whereas MLA infusions yielded an intermediate effect. In addition, neither DHßE nor MLA had an effect on contextual fear conditioning in the absence of systemic nicotine. The present results suggest a critical role for ?4ß2 nAChRs in the dorsal hippocampus for mediating the enhancing effect of nicotine on contextual fear conditioning.
nicotine, hippocampus, nAChRs, addiction, learning, mouse
0270-6474
10870-10877
Davis, Jennifer A.
51c12020-c9a2-4737-bcd6-32bf486e3b53
Kenney, Justin W.
a498bbd6-750d-4778-bd72-6ea336c883e8
Gould, Thomas J.
de84ac91-2b6f-4524-b4d3-1f210047c57a
Davis, Jennifer A.
51c12020-c9a2-4737-bcd6-32bf486e3b53
Kenney, Justin W.
a498bbd6-750d-4778-bd72-6ea336c883e8
Gould, Thomas J.
de84ac91-2b6f-4524-b4d3-1f210047c57a

Davis, Jennifer A., Kenney, Justin W. and Gould, Thomas J. (2007) Hippocampal ?4ß2 nicotinic acetylcholine receptor involvement in the enhancing effect of acute nicotine on contextual fear conditioning. Journal of Neuroscience, 27 (40), 10870-10877. (doi:10.1523/JNEUROSCI.3242-07.2007). (PMID:17913920)

Record type: Article

Abstract

Nicotine is known to enhance learning and memory in hippocampus-dependent tasks such as contextual fear conditioning. The present study was designed to directly examine whether the hippocampus plays a role in mediating this enhancement and which nicotinic acetylcholine receptor (nAChR) subtypes localized to the hippocampus are critical for enhanced learning. Contextual fear conditioning consisted of two white noise conditioned stimuli presentations, each coterminating with a 2 s, 0.57 mA footshock separated by a 120 s intertrial interval. Nicotine (0.09, 0.18, and 0.35 microg per side) was bilaterally infused into the dorsal hippocampus before training and testing. Infusions of nicotine into the dorsal hippocampus produced a dose-dependent enhancement of contextual fear conditioning. To determine which nAChRs are critical to the enhancing effect of nicotine, the preferential ?4ß2 nAChR antagonist, dihydro-beta-erythroidine (DHbetaE) (6.00 and 18.00 microg per side), or the preferential ?7 nAChR antagonist, methyllycaconitine (MLA) (13.50 and 27.00 microg per side), was bilaterally infused into the dorsal hippocampus before systemic injections of nicotine (0.09 mg/kg). DHßE infusions dose-dependently blocked the enhancement of contextual fear conditioning by nicotine, whereas MLA infusions yielded an intermediate effect. In addition, neither DHßE nor MLA had an effect on contextual fear conditioning in the absence of systemic nicotine. The present results suggest a critical role for ?4ß2 nAChRs in the dorsal hippocampus for mediating the enhancing effect of nicotine on contextual fear conditioning.

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More information

Published date: 3 October 2007
Keywords: nicotine, hippocampus, nAChRs, addiction, learning, mouse

Identifiers

Local EPrints ID: 168303
URI: http://eprints.soton.ac.uk/id/eprint/168303
ISSN: 0270-6474
PURE UUID: 58ae5415-2016-4f9b-a9e0-22256eb8fd5f

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Date deposited: 03 Dec 2010 20:54
Last modified: 14 Mar 2024 02:17

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Contributors

Author: Jennifer A. Davis
Author: Justin W. Kenney
Author: Thomas J. Gould

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