Associations between PTSD-Related extinction retention deficits in women and plasma steroids that modulate brain GABA

Allopregnanolone Dehydroepiandrosterone Extinction retention Fear extinction Neurosteroid PTSD Pregnanolone Progesterone

Journal

Neurobiology of stress
ISSN: 2352-2895
Titre abrégé: Neurobiol Stress
Pays: United States
ID NLM: 101643409

Informations de publication

Date de publication:
Nov 2020
Historique:
received: 28 10 2019
revised: 14 04 2020
accepted: 25 04 2020
entrez: 4 6 2020
pubmed: 4 6 2020
medline: 4 6 2020
Statut: epublish

Résumé

Several studies have demonstrated poor retention of extinction learning among individuals with posttraumatic stress disorder (PTSD). Gonadal hormone signaling in brain appears to influence the retention of extinction learning differently in women with and without PTSD. Women with PTSD, compared to trauma-exposed women without PTSD, show relative deficits in extinction retention during the mid-luteal phase (mLP) of the menstrual cycle, compared to the early follicular phase (eFP). A PTSD-related reduction in conversion of progesterone to its GABAergic metabolites allopregnanolone (Allo) and pregnanolone (PA) may contribute to these findings. The current study in trauma-exposed women with (n = 9) and without (n = 9) PTSD investigated associations between extinction retention and plasma Allo + PA levels, as well as the ratio of Allo + PA to 5α-dihydroprogesterone (5α-DHP), the immediate steroid precursor for Allo. The study also investigated the relationship between extinction retention and the ratio of Allo + PA to dehydroepiandrosterone (DHEA), an adrenally-derived GABA

Identifiants

pubmed: 32490055
doi: 10.1016/j.ynstr.2020.100225
pii: S2352-2895(20)30015-1
pii: 100225
pmc: PMC7256058
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100225

Subventions

Organisme : NICHD NIH HHS
ID : K23 HD087428
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH122867
Pays : United States

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Auteurs

Suzanne L Pineles (SL)

National Center for PTSD Women's Health Sciences Division at VA Boston Healthcare System, Boston, MA, 02130, USA.
Department of Psychiatry, Boston University School of Medicine, Boston, MA, 02118, USA.

Yael I Nillni (YI)

National Center for PTSD Women's Health Sciences Division at VA Boston Healthcare System, Boston, MA, 02130, USA.
Department of Psychiatry, Boston University School of Medicine, Boston, MA, 02118, USA.

Graziano Pinna (G)

The Psychiatric Institute, Department of Psychiatry, University of Illinois at Chicago, Chicago, IL, 60612, USA.

Andrea Webb (A)

The Charles Stark Draper Laboratory, Inc., Cambridge, MA, 02139, USA.

Kimberly A Arditte Hall (KA)

Framingham State University, Framingham, MA, 01701, USA.

Jennifer R Fonda (JR)

Translational Research Center for TBI and Stress Disorders (TRACTS) and Geriatric Research, Education and Clinical Center (GRECC), VA Boston Healthcare System Boston, MA, 02130, USA.
Department of Epidemiology, Boston University School of Public Health, Boston, MA, 02118, USA.

John Irvine (J)

The MITRE Corporation, Bedford, MA, 01730, USA.

Matthew W King (MW)

National Center for PTSD Women's Health Sciences Division at VA Boston Healthcare System, Boston, MA, 02130, USA.
Department of Psychiatry, Boston University School of Medicine, Boston, MA, 02118, USA.

Richard L Hauger (RL)

Center of Excellence for Stress and Mental Health, San Diego VA Healthcare System, San Diego, CA, 9216, USA.
Department of Psychiatry, School of Medicine, University of California, San Diego, La Jolla, CA, 92093, USA.

Patricia A Resick (PA)

Department of Psychiatry and Behavioral Sciences, Duke University, Durham, NC, 27701, USA.

Scott P Orr (SP)

Psychiatry Department, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, 02129, USA.

Ann M Rasmusson (AM)

National Center for PTSD Women's Health Sciences Division at VA Boston Healthcare System, Boston, MA, 02130, USA.
Department of Psychiatry, Boston University School of Medicine, Boston, MA, 02118, USA.

Classifications MeSH