Literature DB >> 28675115

Nicotine disrupts safety learning by enhancing fear associated with a safety cue via the dorsal hippocampus.

David A Connor1, Munir G Kutlu1, Thomas J Gould2.   

Abstract

Learned safety, a learning process in which a cue becomes associated with the absence of threat, is disrupted in individuals with post-traumatic stress disorder (PTSD). A bi-directional relationship exists between smoking and PTSD and one potential explanation is that nicotine-associated changes in cognition facilitate PTSD emotional dysregulation by disrupting safety associations. Therefore, we investigated whether nicotine would disrupt learned safety by enhancing fear associated with a safety cue. In the present study, C57BL/6 mice were administered acute or chronic nicotine and trained over three days in a differential backward trace conditioning paradigm consisting of five trials of a forward conditioned stimulus (CS)+ (Light) co-terminating with a footshock unconditioned stimulus followed by a backward CS- (Tone) presented 20 s after cessation of the unconditioned stimulus. Summation testing found that acute nicotine disrupted learned safety, but chronic nicotine had no effect. Another group of animals administered acute nicotine showed fear when presented with the backward CS (Light) alone, indicating the formation of a maladaptive fear association with the backward CS. Finally, we investigated the brain regions involved by administering nicotine directly into the dorsal hippocampus, ventral hippocampus, and prelimbic cortex. Infusion of nicotine into the dorsal hippocampus disrupted safety learning.

Entities:  

Keywords:  Learned safety; backward conditioning; hippocampus; nicotine; prelimbic cortex

Mesh:

Substances:

Year:  2017        PMID: 28675115      PMCID: PMC5755391          DOI: 10.1177/0269881117695861

Source DB:  PubMed          Journal:  J Psychopharmacol        ISSN: 0269-8811            Impact factor:   4.153


  84 in total

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Review 5.  Are the dorsal and ventral hippocampus functionally distinct structures?

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8.  Hippocampal alpha4beta2 nicotinic acetylcholine receptor involvement in the enhancing effect of acute nicotine on contextual fear conditioning.

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  4 in total

1.  Tyrosine receptor kinase B receptor activation reverses the impairing effects of acute nicotine on contextual fear extinction.

Authors:  Munir Gunes Kutlu; Robert D Cole; David A Connor; Brendan Natwora; Thomas J Gould
Journal:  J Psychopharmacol       Date:  2018-03-01       Impact factor: 4.153

2.  Nicotine modulates contextual fear extinction through changes in ventral hippocampal GABAergic function.

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Journal:  Neuropharmacology       Date:  2018-08-28       Impact factor: 5.250

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  4 in total

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