Literature DB >> 28089702

The visible burrow system: A view from across the hall.

James P Herman1, Kellie L Tamashiro2.   

Abstract

The visible burrow system (VBS) is an ethologically relevant social stress model that creates a distinct dominance hierarchy in rats. Randall Sakai's laboratory performed an impressive series of studies documenting the very different impact of VBS exposure on the brain and behavior of dominants (DOM) and subordinates (SUBs). Hierarchy formation causes pronounced changes in metabolism in SUBs relative to both DOMs and unstressed controls, resulting in marked weight loss and metabolic imbalance. Stress testing revealed multiple phenotypes in the VBS, including DOMs, stress-responsive SUBs and stress-non-responsive SUBs. Stress-responsive SUBs have adrenal hypertrophy and elevated baseline corticosterone, consistent with prolonged HPA axis activation; however, peak acute stress responses are not sensitized. In contrast, stress non-responsive individuals do not mount a response to an acute stress, suggesting HPA axis hypofunction. In brain, SUBs exhibit a pattern of gene regulation consistent with impaired stress inhibition (e.g., hippocampal adrenocorticosteroid receptor down-regulation and dendritic retraction) and drive of stress pathways (e.g., increased locus coeruleus tyrosine hydroxylase expression). The non-responsive phenotype is distinguished by down-regulation of paraventricular nucleus corticotropin releasing hormone expression and enhanced neuropeptide Y expression in amygdala. The brain 'signature' created by VBS hierarchy formation differed substantially from that of another well-studied chronic stress model (chronic variable stress). Thus, the impact of VBS is mediated by neurocircuit mechanisms at least in part distinct that of other chronic stress modalities, and suggests that the nature of the stressor may be an essential consideration in development of treatment strategies for stress-related diseases.
Copyright © 2017. Published by Elsevier Inc.

Entities:  

Mesh:

Year:  2017        PMID: 28089702      PMCID: PMC5961943          DOI: 10.1016/j.physbeh.2017.01.021

Source DB:  PubMed          Journal:  Physiol Behav        ISSN: 0031-9384


  57 in total

1.  Meal patterns and hypothalamic NPY expression during chronic social stress and recovery.

Authors:  Susan J Melhorn; Eric G Krause; Karen A Scott; Marie R Mooney; Jeffrey D Johnson; Stephen C Woods; Randall R Sakai
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2010-07-07       Impact factor: 3.619

2.  Daily limited access to sweetened drink attenuates hypothalamic-pituitary-adrenocortical axis stress responses.

Authors:  Yvonne M Ulrich-Lai; Michelle M Ostrander; Ingrid M Thomas; Benjamin A Packard; Amy R Furay; C Mark Dolgas; Daniella C Van Hooren; Helmer F Figueiredo; Nancy K Mueller; Dennis C Choi; James P Herman
Journal:  Endocrinology       Date:  2007-01-04       Impact factor: 4.736

3.  Chronic social subordination stress modulates glutamic acid decarboxylase (GAD) 67 mRNA expression in central stress circuits.

Authors:  Ryan Makinson; Kerstin H Lundgren; Kim B Seroogy; James P Herman
Journal:  Physiol Behav       Date:  2015-07-01

4.  Long-lasting effects of stress on glucocorticoid receptor gene expression in the rat brain.

Authors:  E Kitraki; D Karandrea; C Kittas
Journal:  Neuroendocrinology       Date:  1999-05       Impact factor: 4.914

Review 5.  Interactions between NPY and CRF in the amygdala to regulate emotionality.

Authors:  Tammy J Sajdyk; Anantha Shekhar; Donald R Gehlert
Journal:  Neuropeptides       Date:  2004-08       Impact factor: 3.286

6.  Chronic stress increases pituitary adenylate cyclase-activating peptide (PACAP) and brain-derived neurotrophic factor (BDNF) mRNA expression in the bed nucleus of the stria terminalis (BNST): roles for PACAP in anxiety-like behavior.

Authors:  Sayamwong E Hammack; Joseph Cheung; Kimberly M Rhodes; Kristin C Schutz; William A Falls; Karen M Braas; Victor May
Journal:  Psychoneuroendocrinology       Date:  2009-01-31       Impact factor: 4.905

7.  Norepinephrine-gamma-aminobutyric acid (GABA) interaction in limbic stress circuits: effects of reboxetine on GABAergic neurons.

Authors:  James P Herman; Andrew Renda; Bryan Bodie
Journal:  Biol Psychiatry       Date:  2003-01-15       Impact factor: 13.382

8.  The effect of social stress on hippocampal gene expression.

Authors:  H M Chao; D C Blanchard; R J Blanchard; B S McEwen; R R Sakai
Journal:  Mol Cell Neurosci       Date:  1993-12       Impact factor: 4.314

9.  Corticosterone effects on corticotropin-releasing hormone mRNA in the central nucleus of the amygdala and the parvocellular region of the paraventricular nucleus of the hypothalamus.

Authors:  S Makino; P W Gold; J Schulkin
Journal:  Brain Res       Date:  1994-03-21       Impact factor: 3.252

10.  Effects of chronic social stress on tyrosine hydroxylase mRNA and protein levels.

Authors:  Y Watanabe; C R McKittrick; D C Blanchard; R J Blanchard; B S McEwen; R R Sakai
Journal:  Brain Res Mol Brain Res       Date:  1995-08
View more
  4 in total

Review 1.  Stress in groups: Lessons from non-traditional rodent species and housing models.

Authors:  Annaliese K Beery; Melissa M Holmes; Won Lee; James P Curley
Journal:  Neurosci Biobehav Rev       Date:  2020-04-09       Impact factor: 8.989

2.  Analytic and Interpretational Pitfalls to Measuring Fecal Corticosterone Metabolites in Laboratory Rats and Mice.

Authors:  Neil E Rowland; Linda A Toth
Journal:  Comp Med       Date:  2019-10-02       Impact factor: 0.982

Review 3.  Blueprints for measuring natural behavior.

Authors:  Alicja Puścian; Ewelina Knapska
Journal:  iScience       Date:  2022-06-18

Review 4.  Manifestations of domination: Assessments of social dominance in rodents.

Authors:  Hannah D Fulenwider; Maya A Caruso; Andrey E Ryabinin
Journal:  Genes Brain Behav       Date:  2021-04-11       Impact factor: 3.449

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.