Literature DB >> 29902478

Orexin signaling during social defeat stress influences subsequent social interaction behaviour and recognition memory.

Darrell Eacret1, Laura A Grafe1, Jane Dobkin1, Anthony L Gotter2, John J Renger2, Christopher J Winrow2, Seema Bhatnagar3.   

Abstract

Orexins are neuropeptides synthesized in the lateral hypothalamus that influence arousal, feeding, reward pathways, and the response to stress. However, the role of orexins in repeated stress is not fully characterized. Here, we examined how orexins and their receptors contribute to the coping response during repeated social defeat and subsequent anxiety-like and memory-related behaviors. Specifically, we used Designer Receptors Exclusively Activated by Designer Drugs (DREADDs) to stimulate orexins prior to each of five consecutive days of social defeat stress in adult male rats. Additionally, we determined the role of the orexin 2 receptor in these behaviors by using a selective orexin 2 receptor antagonist (MK-1064) administered prior to each social defeat. Following the 5 day social defeat conditioning period, rats were evaluated in social interaction and novel object recognition paradigms to assess anxiety-like behavior and recognition memory, respectively. Activation of orexin neurons by DREADDs prior to each social defeat decreased the average latency to become defeated across 5 days, indicative of a passive coping strategy that we have previously linked to a stress vulnerable phenotype. Moreover, stimulation of orexin signaling during defeat conditioning decreased subsequent social interaction and performance in the novel object recognition test indicating increased subsequent anxiety-like behavior and reduced recognition memory. Blocking the orexin 2 receptor during repeated defeat did not alter these effects. Together, our results suggest that orexin neuron activation produces a passive coping phenotype during social defeat leading to subsequent anxiety-like behaviors and memory deficits.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  DREADDs; Hypocretin; Orexin; Stress

Mesh:

Substances:

Year:  2018        PMID: 29902478     DOI: 10.1016/j.bbr.2018.05.032

Source DB:  PubMed          Journal:  Behav Brain Res        ISSN: 0166-4328            Impact factor:   3.332


  9 in total

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Review 4.  Orexin/hypocretin receptor modulation of anxiolytic and antidepressive responses during social stress and decision-making: Potential for therapy.

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Review 5.  Evolution of stress responses refine mechanisms of social rank.

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Journal:  Neurobiol Stress       Date:  2021-04-21

Review 6.  Cardinal role of the environment in stress induced changes across life stages and generations.

Authors:  Terence Y Pang; Jazmine D W Yaeger; Cliff H Summers; Rupshi Mitra
Journal:  Neurosci Biobehav Rev       Date:  2021-02-04       Impact factor: 9.052

7.  Brain histamine and oleoylethanolamide restore behavioral deficits induced by chronic social defeat stress in mice.

Authors:  Barbara Rani; Andrea Santangelo; Adele Romano; Justyna Barbara Koczwara; Marzia Friuli; Gustavo Provensi; Patrizio Blandina; Maurizio Casarrubea; Silvana Gaetani; Maria Beatrice Passani; Alessia Costa
Journal:  Neurobiol Stress       Date:  2021-03-17

8.  The role of basolateral amygdala orexin 1 receptors on the modulation of pain and psychosocial deficits in nitroglycerin-induced migraine model in adult male rats.

Authors:  Khadijeh Askari-Zahabi; Mehdi Abbasnejad; Razieh Kooshki; Maryam Raoof; Saeed Esmaeili-Mahani; Ali Mohammad Pourrahimi; Mahnaz Zamyad
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9.  Developmental differences in amygdala projection neuron activation associated with isolation-driven changes in social preference.

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  9 in total

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