Literature DB >> 21112345

Activation patterns of cells in selected brain stem nuclei of more and less stress responsive rats in two animal models of PTSD - predator exposure and submersion stress.

Robert Adamec1, Mate Toth, Jozsef Haller, Jozsef Halasz, Jacqueline Blundell.   

Abstract

This study had two purposes. First: compare predator and water submersion stress cFos activation patterns in dorsal raphe (DR), locus coeruleus (LC) and periaqueductal gray (PAG). Second: identify markers of vulnerability to stressors within these areas. Rats were either predator or submersion stressed and tested 1.75 h later for anxiety-like behavior. Immediately thereafter, rats were sacrificed and cFos expression examined. In DR, serotonergic cells expressing or not expressing cFos were also counted. Predator and submersion stress increased anxiety-like behavior (in the elevated plus maze- EPM) equally over controls. Moreover, stressed rats spent equally less time in the center of the hole board than handled controls, another indication of increased anxiety-like behavior. To examine vulnerability, rats which were less anxious (LA) and more (highly) anxious (MA) in the EPM were selected from among handled control and stressed animals. LA rats in the stressed groups were considered stress non-responsive and MA stressed rats were considered stress responsive. LA and MA rats did not differ in cFos expression in any brain area, though stressors did increase cFos cell counts in all areas over controls. Intriguingly, the number of serotonergic DR neurons not activated by stress predicted degree of anxiety response to submersion stress only. LA submersion stressed rats had more serotonergic cells than all other groups, and MA submersion stressed rats had fewer serotonergic cells than all other groups, which did not differ. Moreover, these cell counts correlated with EPM anxiety. We conclude that a surplus of such cells protects against anxiogenic effects of submersion, while a paucity of such cells enhances vulnerability to submersion stress. Other data suggest serotonergic cells may exert their effects via inhibition of dorsolateral PAG cells during submersion stress. Findings are discussed with respect to serotonergic transmission in vulnerability to predator stress and relevance of findings for post traumatic stress disorder (PTSD). This article is part of a Special Issue entitled 'Post-Traumatic Stress Disorder'.
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 21112345     DOI: 10.1016/j.neuropharm.2010.11.018

Source DB:  PubMed          Journal:  Neuropharmacology        ISSN: 0028-3908            Impact factor:   5.250


  9 in total

1.  Live predator stress in adolescence results in distinct adult behavioral consequences and dorsal diencephalic brain activation patterns.

Authors:  J D Tapocik; J R Schank; J R Mitchell; R Damazdic; C L Mayo; D Brady; A B Pincus; C E King; M Heilig; G I Elmer
Journal:  Behav Brain Res       Date:  2020-12-09       Impact factor: 3.332

2.  Fos expression following regimens of predator stress versus footshock that differentially affect prepulse inhibition in rats.

Authors:  Sarah K Baisley; Christina L Cloninger; Vaishali P Bakshi
Journal:  Physiol Behav       Date:  2011-08-06

3.  The effect of short-term stress on serotonin gene expression in high and low resilient macaques.

Authors:  Cynthia L Bethea; Kenny Phu; Arubala P Reddy; Judy L Cameron
Journal:  Prog Neuropsychopharmacol Biol Psychiatry       Date:  2013-01-26       Impact factor: 5.067

4.  Endocannabinoid modulating drugs improve anxiety but not the expression of conditioned fear in a rodent model of post-traumatic stress disorder.

Authors:  Akshayan Vimalanathan; Darryl C Gidyk; Mustansir Diwan; Flavia V Gouveia; Nir Lipsman; Peter Giacobbe; José N Nobrega; Clement Hamani
Journal:  Neuropharmacology       Date:  2020-01-13       Impact factor: 5.250

5.  Anxiolytic effects and neuroanatomical targets of estrogen receptor-β (ERβ) activation by a selective ERβ agonist in female mice.

Authors:  Mario G Oyola; Wendy Portillo; Andrea Reyna; Chad D Foradori; Andrea Kudwa; Laura Hinds; Robert J Handa; Shaila K Mani
Journal:  Endocrinology       Date:  2011-12-20       Impact factor: 4.736

6.  fMRI functional connectivity of the periaqueductal gray in PTSD and its dissociative subtype.

Authors:  Sherain Harricharan; Daniela Rabellino; Paul A Frewen; Maria Densmore; Jean Théberge; Margaret C McKinnon; Allan N Schore; Ruth A Lanius
Journal:  Brain Behav       Date:  2016-09-20       Impact factor: 2.708

Review 7.  Animal models of PTSD: a challenge to be met.

Authors:  Gal Richter-Levin; Oliver Stork; Mathias V Schmidt
Journal:  Mol Psychiatry       Date:  2018-10-19       Impact factor: 15.992

Review 8.  Making memories of stressful events: a journey along epigenetic, gene transcription, and signaling pathways.

Authors:  Johannes M H M Reul
Journal:  Front Psychiatry       Date:  2014-01-22       Impact factor: 4.157

9.  Administration of NaHS Attenuates Footshock-Induced Pathologies and Emotional and Cognitive Dysfunction in Triple Transgenic Alzheimer's Mice.

Authors:  Hei-Jen Huang; Shu-Ling Chen; Hsiu Mei Hsieh-Li
Journal:  Front Behav Neurosci       Date:  2015-11-25       Impact factor: 3.558

  9 in total

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