Childhood stress impairs social function through AVP-dependent mechanisms.


Journal

Translational psychiatry
ISSN: 2158-3188
Titre abrégé: Transl Psychiatry
Pays: United States
ID NLM: 101562664

Informations de publication

Date de publication:
09 12 2019
Historique:
received: 21 08 2019
accepted: 27 11 2019
revised: 19 11 2019
entrez: 11 12 2019
pubmed: 11 12 2019
medline: 22 9 2020
Statut: epublish

Résumé

Impaired social function is a core feature of many psychiatric illnesses. Adverse experiences during childhood increase risk for mental illness, however it is currently unclear whether stress early in life plays a direct role in the development of social difficulties. Using a rat model of pre-pubertal stress (PPS), we investigated effects on social behaviour, oxytocin and arginine vasopressin (AVP) in the periphery (plasma) and centrally in the paraventricular and supraoptic hypothalamic nuclei. We also explored social performance and AVP expression (plasma) in participants with borderline personality disorder (BPD) who experienced a high incidence of childhood stress. Social behaviour was impaired and AVP expression increased in animals experiencing PPS and participants with BPD. Behavioural deficits in animals were rescued through administration of the AVPR1a antagonist Relcovaptan (SR49059). AVP levels and recognition of negative emotions were significantly correlated in BPD participants only. In conclusion, early life stress plays a role in the precipitation of social dysfunction, and AVP mediates at least part of this effect.

Identifiants

pubmed: 31819033
doi: 10.1038/s41398-019-0678-0
pii: 10.1038/s41398-019-0678-0
pmc: PMC6901493
doi:

Substances chimiques

AVP protein, human 0
Antidiuretic Hormone Receptor Antagonists 0
Indoles 0
Neurophysins 0
Protein Precursors 0
Pyrrolidines 0
Vasopressins 11000-17-2
Arginine Vasopressin 113-79-1
relcovaptan C1GL8G6G0O

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

330

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Auteurs

Nichola M Brydges (NM)

Neuroscience and Mental Health Research Institute, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, UK. brydgesn@cardiff.ac.uk.

Jessica Hall (J)

National Centre for Mental Health, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, UK.

Caroline Best (C)

Neuroscience and Mental Health Research Institute, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, UK.

Lowenna Rule (L)

Neuroscience and Mental Health Research Institute, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, UK.

Holly Watkin (H)

Neuroscience and Mental Health Research Institute, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, UK.

Amanda J Drake (AJ)

University/BHF Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.

Catrin Lewis (C)

National Centre for Mental Health, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, UK.

Kerrie L Thomas (KL)

Neuroscience and Mental Health Research Institute, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, UK.
School of Biosciences, Cardiff University, Museum Avenue, Cardiff, CF10 3AX, UK.

Jeremy Hall (J)

Neuroscience and Mental Health Research Institute, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, UK.
MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, UK.

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