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d-Cycloserine facilitates context-specific fear extinction learning

Open access
Bouton, Mark E., Vurbic, Drina, Woods, Amanda M.·2008·Neurobiology of Learning and Memory

Abstract

D-cycloserine (DCS) may facilitate fear extinction learning, but the behavioral consequences and mechanisms behind this effect are not well understood at present. In this paper, we re-analyze data from previously reported null result experiments and find that rats showing above-median extinction learning during DCS treatment benefited from the drug, whereas rats showing below-median (and in this case little) extinction learning did not. Two additional experiments found that DCS facilitated extinction learning when specifically combined with a moderate, but not a small, number of extinction trials. DCS thus facilitates extinction learning only if the behavioral procedure first engages the extinction learning process. The benefits of the drug, however, were specific to the context in which extinction was learned--i.e., DCS did not prevent or influence the renewal of fear observed when the extinguished cue was tested in the original conditioning context.

Overview

AI snapshot

Written from the paper’s full text.

TL;DR

D-cycloserine (DCS) facilitated fear extinction only when the extinction procedure first engaged learning: rats that learned some extinction during the drug session benefited, and DCS helped with 12 but not 2 extinction trials. The benefit was context-specific and did not reduce renewal of fear in the original conditioning context.

Key findings

  • In Experiment 1, a median split showed that rats above the median learned extinction during the DCS session, with a significant decrease in suppression across trial blocks, F(1, 22) = 54.80, whereas below-median rats did not, F(1, 22) < 1. DCS facilitated later test extinction only in above-median rats (group × block interaction, F(3, 66) = 2.95; significant on the second block, F(1, 22) = 4.73), with no DCS effect in below-median rats.
  • In Experiment 2A, DCS facilitated extinction in the 12-trial group, F(1, 15) = 4.76, but not in the 2-trial group, F(1, 15) < 1. In Experiment 2B, the 12-trial DCS effect was F(1, 15) = 3.87, p = .03, one-tailed; pooled across 2A and 2B it was F(1, 31) = 8.69, two-tailed p = .006, while the 2-trial group did not approach significance, F < 1.
  • DCS did not influence renewal. In Experiment 2A, renewal testing in Context A showed a significant difference between tests, F(1, 15) = 14.58, with no drug effect or interaction, Fs ≤ 2.01. In Experiment 2B, there were no drug effects or interactions, Fs ≤ 1.71, while freezing increased in Context A, F(1, 15) = 3.97, p = .03, one-tailed; pooled across 2A and 2B, F(1, 31) = 14.41, two-tailed p = .001.

Methods

  • Experiment 1 used 48 female Wistar rats in a conditioned suppression procedure. Rats received fear conditioning in Context A, then four CS-alone extinction trials in Context B with DCS 30 mg/kg or saline injected 15 min before the session; tests occurred in Context B, and a median split on drug-session suppression ratios classified above- versus below-median extinction learning.
  • Experiments 2A and 2B used 64 naive female Wistar rats (32 each). Rats received fear conditioning with two CSs in Context A; one CS was extinguished with saline in Context B and the other with DCS in Context C, with either 12 or 2 extinction trials and DCS doses of 15 or 30 mg/kg. Freezing was scored every 2 s, with interobserver correlations of r(62) = .97 and .92 for Experiments 2A and 2B; tests occurred in the extinction contexts and then in Context A for renewal.
  • Statistical analysis used ANOVA with rejection criterion p < .05.

Limitations

  • The paper states that Experiment 1 was correlational and could have been controlled by an unidentified third variable; Experiment 2 was designed to isolate the combination of DCS and CS re-exposure experimentally.
  • The paper notes that its results did not replicate Lee et al.’s (2006) finding that DCS increased fear with minimal extinction training, and it lists procedural differences including number of CS re-exposures, session duration, and whether re-exposure occurred in a different context.
  • Evident from the text: the experiments used only female Wistar rats, specific fear-conditioning preparations (conditioned suppression and conditioned freezing), limited DCS doses, and particular trial numbers, so the boundary conditions may not generalize beyond these procedures.

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Integrity signals

Registry

Crossref · 10.1016/j.nlm.2008.07.003

Cites

31 of 31 references verified0 citation errors · 0 not checkable

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Claims the paper makes

10 Not checked yet · 8 Own result · 7 Own interpretation · 3 Own method

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Show all 21 claims

  • It may state two separate claims as one. 6
  • Probably not a substantial claim. 3
7 of 7
  • The paper relies on this without support.

    DCS is present in the brain during the extinction session when administered 15 minutes before the session.

    “the effectiveness of DCS was predicted by the extent to which animals learned extinction during the drug session (while the drug was in the brain)”
  • The paper relies on this without support.

    The renewal test had sufficient sensitivity or power to detect a DCS effect on renewal if such an effect were present.

    “DCS did not influence the strength of the renewal effect observed when the animals were tested with the CSs in Context A.”
2 of 2

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Statistics recomputed

Every reported test result, recomputed from its test statistic and degrees of freedom. A result shows as not adding up only once an independent check has confirmed it.

  • ConsistentF(1, 15) = 3.87reported p = .03 · recomputed p = .068

    “F(1,15) = 3.87, p = .03”

    The paper states a one-tailed test

  • ConsistentF(1, 15) = 3.97reported p = .03 · recomputed p = .065

    “F (1,15) = 3.97, p = .03”

    The paper states a one-tailed test

2 of 2

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

Each contradiction between two passages listed here was confirmed by an independent check.

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Metadata

Authors
Bouton, M. E., Vurbic, D., & Woods, A. M.
Affiliations
University of Vermont (US)
Corresponding author
Bouton, Mark E.
Venue
Neurobiology of Learning and Memory
Publisher
Elsevier BV
Published
2008-10
Volume
90
Issue
3
Pages
504-510
ISSN
1074-7427 (ISSN-L)
OpenAlex
W2076008075
Cited by
118
References
32
Citations by year
2026: 2 · 2025: 1 · 2024: 3 · 2023: 2 · 2022: 4 · 2021: 2 · 2020: 1 · 2019: 4 · 2018: 5 · 2017: 11 · 2016: 4 · 2015: 9 · 2014: 16 · 2013: 11 · 2012: 15
FWCI
4.65
Type
journal article
Language
en
Open access
Locations
  • Neurobiology of Learning and Memory (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Institute of Mental Health
Topics
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords
D-cycloserine, fear extinction, extinction learning, fear renewal
MeSH terms
Animals, Antimetabolites, Association Learning, Behavior, Animal, Conditioning, Classical, Cycloserine, Environment, Extinction, Psychological, Fear, Female, Rats, Wistar, Rats

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