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Gating of the neuroendocrine stress responses by stressor salience in early lactating female rats is independent of infralimbic cortex activation and plasticity.

Author(s): Hillerer KM, Woodside B, Parkinson E, Long H, Verlezza S, Walker CD

Stress. 2018 05;21(3):217-228 Authors: Hillerer KM, Woodside B, Parkinson E, Long H, Verlezza S, Walker CD

Article GUID: 29397787

Intranasal oxytocin and salivary cortisol concentrations during social rejection in university students.

Author(s): Linnen AM, Ellenbogen MA, Cardoso C, Joober R

Stress. 2012 Jul;15(4):393-402 Authors: Linnen AM, Ellenbogen MA, Cardoso C, Joober R

Article GUID: 22044077

Sexual orientation, disclosure, and cardiovascular stress reactivity.

Author(s): Juster RP, Doyle DM, Hatzenbuehler ML, Everett BG, DuBois LZ, McGrath JJ

Stress. 2019 May;22(3):321-331 Authors: Juster RP, Doyle DM, Hatzenbuehler ML, Everett BG, DuBois LZ, McGrath JJ

Article GUID: 30835598


Title:Gating of the neuroendocrine stress responses by stressor salience in early lactating female rats is independent of infralimbic cortex activation and plasticity.
Authors:Hillerer KMWoodside BParkinson ELong HVerlezza SWalker CD
Link:https://www.ncbi.nlm.nih.gov/pubmed/29397787?dopt=Abstract
DOI:10.1080/10253890.2018.1434618
Category:Stress
PMID:29397787
Dept Affiliation: CSBN
1 a Department of Psychiatry , McGill University, Douglas Mental Health University Institute , Montreal , Canada.
2 b Department of Obstetrics and Gynaecology , Paracelsus Medical University , Salzburg , Austria.
3 c Center for Studies in Behavioral Neurobiology, Concordia University , Montreal , Canada.

Description:

Gating of the neuroendocrine stress responses by stressor salience in early lactating female rats is independent of infralimbic cortex activation and plasticity.

Stress. 2018 05;21(3):217-228

Authors: Hillerer KM, Woodside B, Parkinson E, Long H, Verlezza S, Walker CD

Abstract

In early lactation (EL), stressor salience modulates neuroendocrine stress responses, but it is unclear whether this persists throughout lactation and which neural structures are implicated. We hypothesized that this process is specific to EL and that the infralimbic (IL) medial prefrontal cortex (mPFC) might provide a critical link between assessment of threat and activation of the hypothalamo-pituitary-adrenal (HPA) axis in EL. We measured neuroendocrine responses and neuronal Fos induction to a salient (predator odor) or non-salient (tail pinch) psychogenic stressor in EL and late lactation (LL) females. We found that EL females exhibited a large response to predator stress only in the presence of pups, while responses to tail pinch were reduced independently of pup presence. In LL, HPA axis responses were independent of pup presence for both stressors and only responses to tail pinch were modestly reduced compared to virgins. Intracerebral injection of the local anesthetic bupivacaine (BUP) (0.75%; 0.5 µl/side) in the IL mPFC did not differentially affect neuroendocrine responses to predator odor in virgin and EL females, suggesting that lactation-induced changes in this structure might not regulate stressor salience for the HPA axis. However, the IL mPFC displayed morphological changes in lactation, with significant increases in dendritic spine numbers and density in EL compared to LL and virgin females. EL females also showed improved performance in the attention set-shifting task (AST), which could reflect early plasticity in the IL mPFC at a time when rapid adaptation of the maternal brain is necessary for pup survival.

PMID: 29397787 [PubMed - indexed for MEDLINE]