Literature DB >> 26348715

Effects of extinction treatments on the reduction of conditioned responding and conditioned hyperarousal in a rabbit model of posttraumatic stress disorder (PTSD).

Lauren B Burhans1, Carrie A Smith-Bell1, Bernard G Schreurs1.   

Abstract

We have previously characterized a model of posttraumatic stress disorder (PTSD), based on classical conditioning of the rabbit nictitating membrane response (NMR), that focuses on 2 key PTSD-like features: conditioned responses to trauma-associated cues and hyperarousal. In addition to the development of conditioned NMRs (CRs) to a tone conditioned stimulus (CS) associated with a periorbital shock unconditioned stimulus (US), we have observed that rabbits also exhibit a conditioning-specific reflex modification (CRM) of the NMR that manifests as an exaggerated and more complex reflexive NMR to presentations of the US by itself, particularly to intensities that elicited little response prior to conditioning. Previous work has demonstrated that unpaired presentations of the CS and US are successful at extinguishing CRs and CRM simultaneously, even when a significantly weakened version of the US is utilized. In the current study, additional extinction treatments were tested, including continued pairings of the CS with a weakened US and exposure to the training context alone, and these treatments were contrasted with the effects of unpaired extinction with a weakened US and remaining in home cages with no further treatment. Results showed that continued pairings only slightly decreased CRs and CRM, while context exposure had no effect on CRs and marginal effects on reducing CRM. Unpaired extinction was still the most effective treatment for reducing both. Findings are discussed in terms of applications to cognitive-behavioral therapies for treatment of PTSD, such as incorporating mild, innately stressful stimuli into virtual reality therapy. (c) 2015 APA, all rights reserved).

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Year:  2015        PMID: 26348715      PMCID: PMC4667790          DOI: 10.1037/bne0000092

Source DB:  PubMed          Journal:  Behav Neurosci        ISSN: 0735-7044            Impact factor:   1.912


  56 in total

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2.  Comparing excitatory backward and forward conditioning.

Authors:  Raymond C Chang; Steven Stout; Ralph R Miller
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Review 3.  Neural substrates of eyeblink conditioning: acquisition and retention.

Authors:  Kimberly M Christian; Richard F Thompson
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4.  Covariation of alternative measures of responding in rabbit (Oryctolagus cuniculus) eyeblink conditioning during acquisition training and tone generalization.

Authors:  Keith S Garcia; Michael D Mauk; Gabrielle Weidemann; E James Kehoe
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5.  Apparatus exposure produces profound declines in conditioned nictitating-membrane responses to discrete conditioned stimuli by the rabbit (Oryctolagus cuniculus).

Authors:  E James Kehoe; Gabrielle Weidemann; Stephanie Dartnall
Journal:  J Exp Psychol Anim Behav Process       Date:  2004-10

6.  Conditioning-specific reflex modification of the rabbit (Oryctolagus cuniculus) nictitating membrane response: US intensity effects.

Authors:  Matthew A Seager; Carrie A Smith-Bell; Bernard G Schreurs
Journal:  Learn Behav       Date:  2003-08       Impact factor: 1.986

7.  Reflex facilitation during eyeblink conditioning and subsequent interpositus nucleus inactivation in the rabbit (Oryctolagus cuniculus).

Authors:  Jan Wikgren; Timo Ruusuvirta; Tapani Korhonen
Journal:  Behav Neurosci       Date:  2002-12       Impact factor: 1.912

Review 8.  Classical conditioning and modification of the rabbit's (Oryctolagus cuniculus) unconditioned nictitating membrane response.

Authors:  Bernard G Schreurs
Journal:  Behav Cogn Neurosci Rev       Date:  2003-06

9.  Fear conditioning in virtual reality contexts: a new tool for the study of anxiety.

Authors:  Johanna M Baas; Monique Nugent; Shmuel Lissek; Daniel S Pine; Christian Grillon
Journal:  Biol Psychiatry       Date:  2004-06-01       Impact factor: 13.382

10.  Classical conditioning of the rabbit's (Oryctolagus cuniculus) nictitating membrane response under symmetrical CS-US interval shifts.

Authors:  S R Coleman; I Gormezano
Journal:  J Comp Physiol Psychol       Date:  1971-12
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  5 in total

1.  Delayed unpaired extinction as a treatment for hyperarousal of the rabbit nictitating membrane response and its implications for treating PTSD.

Authors:  Bernard G Schreurs; Carrie A Smith-Bell; Lauren B Burhans
Journal:  J Psychiatr Res       Date:  2018-01-12       Impact factor: 4.791

2.  Sex differences in a rabbit eyeblink conditioning model of PTSD.

Authors:  Bernard G Schreurs; Carrie Smith-Bell; Lauren B Burhans
Journal:  Neurobiol Learn Mem       Date:  2018-04-24       Impact factor: 2.877

3.  Propranolol produces short-term facilitation of extinction in a rabbit model of post-traumatic stress disorder.

Authors:  Lauren B Burhans; Carrie A Smith-Bell; Bernard G Schreurs
Journal:  Neuropharmacology       Date:  2018-03-23       Impact factor: 5.250

4.  Inactivation of the interpositus nucleus blocks the acquisition of conditioned responses and timing changes in conditioning-specific reflex modification of the rabbit eyeblink response.

Authors:  Lauren B Burhans; Bernard G Schreurs
Journal:  Neurobiol Learn Mem       Date:  2018-07-24       Impact factor: 2.877

5.  Inactivation of the interpositus nucleus during unpaired extinction does not prevent extinction of conditioned eyeblink responses or conditioning-specific reflex modification.

Authors:  Lauren B Burhans; Bernard G Schreurs
Journal:  Behav Neurosci       Date:  2019-03-14       Impact factor: 1.912

  5 in total

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