Literature DB >> 21256147

The use of cognitive enhancers in animal models of fear extinction.

Gary B Kaplan1, Katherine A Moore.   

Abstract

In anxiety disorders, such as posttraumatic stress disorders and phobias, classical conditioning pairs natural (unconditioned) fear-eliciting stimuli with contextual or discrete cues resulting in enduring fear responses to multiple stimuli. Extinction is an active learning process that results in a reduction of conditioned fear responses after conditioned stimuli are no longer paired with unconditioned stimuli. Fear extinction often produces incomplete effects and this highlights the relative permanence of bonds between conditioned stimuli and conditioned fear responses. The animal research literature is rich in its demonstration of cognitive enhancing agents that alter fear extinction. This review specifically examines the fear extinguishing effects of cognitive enhancers that act on gamma-aminobutyric acid (GABA), glutamatergic, cholinergic, adrenergic, dopaminergic, and cannabinoid signaling pathways. It also examines the effects of compounds that alter epigenetic and neurotrophic mechanisms in fear extinction. Of these cognitive enhancers, glutamatergic N-methyl d-aspartate (NMDA) receptor agonists, such as D-cycloserine, have enhanced fear extinction in a context-, dose- and time-dependent manner. Agents that function as glutamatergic α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor agonists, alpha2-adrenergic receptor antagonists (such as yohimbine), neurotrophic factors (brain derived neurotrophic factor or BDNF) and histone deacetylase inhibitors (valproate and sodium butyrate) also improve fear extinction in animals. However, some have anxiogenic effects and their contextual and temporal effects need to be more reliably demonstrated. Various cognitive enhancers produce changes in cortico-amygdala synaptic plasticity through multiple mechanisms and these neural changes enhance fear extinction. We need to better define the changes in neural plasticity produced by these agents in order to develop more effective compounds. In the clinical setting, such use of effective cognitive enhancers with cue exposure therapy, using compounds derived from animal model studies, provides great hope for the future treatment of anxiety disorders. Published by Elsevier Inc.

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Year:  2011        PMID: 21256147     DOI: 10.1016/j.pbb.2011.01.009

Source DB:  PubMed          Journal:  Pharmacol Biochem Behav        ISSN: 0091-3057            Impact factor:   3.533


  43 in total

1.  Changes in expression of c-Fos protein following cocaine-cue extinction learning.

Authors:  B Á Nic Dhonnchadha; B F Lovascio; N Shrestha; A Lin; K A Leite-Morris; H Y Man; G B Kaplan; K M Kantak
Journal:  Behav Brain Res       Date:  2012-06-18       Impact factor: 3.332

2.  Nicotine- and cocaine-triggered methamphetamine reinstatement in female and male Sprague-Dawley rats.

Authors:  Steven T Pittenger; Shinnyi Chou; Scott T Barrett; Isabella Catalano; Maxwell Lydiatt; Rick A Bevins
Journal:  Pharmacol Biochem Behav       Date:  2017-07-13       Impact factor: 3.533

Review 3.  Generating new neurons to circumvent your fears: the role of IGF signaling.

Authors:  R C Agis-Balboa; A Fischer
Journal:  Cell Mol Life Sci       Date:  2013-03-30       Impact factor: 9.261

4.  Comprehensive analysis of transcription dynamics from brain samples following behavioral experience.

Authors:  Hagit Turm; Diptendu Mukherjee; Doron Haritan; Maayan Tahor; Ami Citri
Journal:  J Vis Exp       Date:  2014-08-26       Impact factor: 1.355

Review 5.  Nicotinic Acetylcholine Receptor Ligands, Cognitive Function, and Preclinical Approaches to Drug Discovery.

Authors:  Alvin V Terry; Patrick M Callahan
Journal:  Nicotine Tob Res       Date:  2019-02-18       Impact factor: 4.244

6.  Cannabinoid modulation of prefrontal-limbic activation during fear extinction learning and recall in humans.

Authors:  Christine A Rabinak; Mike Angstadt; Maryssa Lyons; Shoko Mori; Mohammed R Milad; Israel Liberzon; K Luan Phan
Journal:  Neurobiol Learn Mem       Date:  2013-09-19       Impact factor: 2.877

7.  The context dependency of extinction negates the effectiveness of cognitive enhancement to reduce cocaine-primed reinstatement.

Authors:  Sherri Hammond; John J Wagner
Journal:  Behav Brain Res       Date:  2013-06-21       Impact factor: 3.332

8.  Epigenetic priming of memory updating during reconsolidation to attenuate remote fear memories.

Authors:  Johannes Gräff; Nadine F Joseph; Meryl E Horn; Alireza Samiei; Jia Meng; Jinsoo Seo; Damien Rei; Adam W Bero; Trongha X Phan; Florence Wagner; Edward Holson; Jinbin Xu; Jianjun Sun; Rachael L Neve; Robert H Mach; Stephen J Haggarty; Li-Huei Tsai
Journal:  Cell       Date:  2014-01-16       Impact factor: 41.582

9.  Vorinostat ameliorates impaired fear extinction possibly via the hippocampal NMDA-CaMKII pathway in an animal model of posttraumatic stress disorder.

Authors:  Yasutaka Matsumoto; Shigeru Morinobu; Shigeto Yamamoto; Tomoya Matsumoto; Shiro Takei; Yosuke Fujita; Shigeto Yamawaki
Journal:  Psychopharmacology (Berl)       Date:  2013-04-13       Impact factor: 4.530

10.  The histone deacetylase inhibitor sodium butyrate modulates acquisition and extinction of cocaine-induced conditioned place preference.

Authors:  Jonathan D Raybuck; Ellen J McCleery; Christopher L Cunningham; Marcelo A Wood; K Matthew Lattal
Journal:  Pharmacol Biochem Behav       Date:  2013-02-27       Impact factor: 3.533

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