Recent progress in understanding the pathophysiology of post-traumatic stress disorder: implications for targeted pharmacological treatment.
Source
Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Abstract
Post-traumatic stress disorder (PTSD) is a common and chronic anxiety disorder that can result after exposure to a traumatic event. Though our understanding of the aetiology of PTSD is incomplete, several neurobiological systems have been implicated in the pathophysiology and vulnerability towards developing PTSD after trauma exposure. We aimed to provide a concise review of benchmark findings in important neurobiological systems related to the aetiology and maintenance of PTSD symptomology. Specifically, we discuss functional aetiologies in the noradrenergic, serotonergic, endogenous cannabinoid and opioid systems as well as the hypothalamic-pituitary adrenal (HPA) axis. This article provides a succinct framework to appreciate the current understanding of neurobiological mechanisms related to the pathophysiology of PTSD and how these findings may impact the development of future, targeted pharmacological treatments for this debilitating disorder.
- PMID:
- 23483368
- [PubMed – indexed for MEDLINE]
- PMCID:
- PMC3629370
- [Available on 2014/3/1]
Publication Types, MeSH Terms, Grant Support
Publication Types
MeSH Terms
- Animals
- Drug Design*
- Female
- Humans
- Hypothalamo-Hypophyseal System/metabolism
- Male
- Molecular Targeted Therapy*
- Pituitary-Adrenal System/metabolism
- Stress Disorders, Post-Traumatic/drug therapy
- Stress Disorders, Post-Traumatic/etiology
- Stress Disorders, Post-Traumatic/physiopathology*
Grant Support
- R01 MH096876/MH/NIMH NIH HHS/United States
- R01 MH096876-01A1/MH/NIMH NIH HHS/United States
- R21 MH081103/MH/NIMH NIH HHS/United States
- R21 MH081103/MH/NIMH NIH HHS/United States
- R21 MH085627/MH/NIMH NIH HHS/United States
- R21 MH085627/MH/NIMH NIH HHS/United States
- R21 MH096105/MH/NIMH NIH HHS/United States
- R21 MH096105-01A1/MH/NIMH NIH HHS/United States