Literature DB >> 25773140

Investigational drugs under development for the treatment of PTSD.

Benjamin J Ragen1, Jordan Seidel, Christine Chollak, Robert H Pietrzak, Alexander Neumeister.   

Abstract

INTRODUCTION: Posttraumatic stress disorder (PTSD) is a prevalent, chronic and disabling anxiety disorder that may develop following exposure to a traumatic event. There is currently no effective pharmacotherapy for PTSD and therefore the discovery of novel, evidence-based treatments is particularly important. This review of potential novel treatments could act as a catalyst for further drug investigation. AREAS COVERED: In this review, the authors discuss the heterogeneity of PTSD and why this provides a challenge for discovering effective treatments for this disorder. By searching for the neurobiological systems that are disrupted in individuals with PTSD and their correlation with different symptoms, the authors propose potential pharmacological treatments that could target these symptoms. They discuss drugs such as nabilone, d-cycloserine, nor-BNI, 7,8-dihydroxyflavone and oxytocin (OT) to target systems such as cannabinoids, glutamate, opioids, brain-derived neurotrophic factor and the OT receptor, respectively. While not conclusive, the authors believe that these brain systems include promising targets for drug discovery. Finally, the authors review animal studies, proof-of-concept studies and case studies that support our proposed treatments. EXPERT OPINION: A mechanism-based approach utilizing techniques such as in vivo neuroimaging will allow for the determination of treatments. Due to the heterogeneity of the PTSD phenotype, focusing on symptomology rather than a categorical diagnosis will allow for more personalized treatment. Furthermore, there appears to be a promise in drugs as cognitive enhancers, the use of drug cocktails and novel compounds that target specific pathways linked to the etiology of PTSD.

Entities:  

Keywords:  evidence-based; neurobiology; posttraumatic stress disorder; treatment

Mesh:

Substances:

Year:  2015        PMID: 25773140     DOI: 10.1517/13543784.2015.1020109

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  7 in total

Review 1.  Glutamate dysregulation and glutamatergic therapeutics for PTSD: Evidence from human studies.

Authors:  Lynnette A Averill; Prerana Purohit; Christopher L Averill; Markus A Boesl; John H Krystal; Chadi G Abdallah
Journal:  Neurosci Lett       Date:  2016-12-01       Impact factor: 3.046

Review 2.  Cannabidiol as a Potential Treatment for Anxiety Disorders.

Authors:  Esther M Blessing; Maria M Steenkamp; Jorge Manzanares; Charles R Marmar
Journal:  Neurotherapeutics       Date:  2015-10       Impact factor: 7.620

3.  Oxytocin differentially modulates pavlovian cue and context fear acquisition.

Authors:  Juliana Cavalli; Michaela Ruttorf; Mario Rosero Pahi; Francesca Zidda; Herta Flor; Frauke Nees
Journal:  Soc Cogn Affect Neurosci       Date:  2017-06-01       Impact factor: 3.436

Review 4.  Animal models of PTSD: a challenge to be met.

Authors:  Gal Richter-Levin; Oliver Stork; Mathias V Schmidt
Journal:  Mol Psychiatry       Date:  2018-10-19       Impact factor: 15.992

5.  7,8-Dihydroxyflavone protects neurons against oxygen-glucose deprivation induced apoptosis and activates the TrkB/Akt pathway.

Authors:  Qinxiang Zhou; Hao Tang; Dingqun Bai; Yuhan Kong
Journal:  PeerJ       Date:  2022-02-15       Impact factor: 2.984

6.  7, 8-Dihydroxyflavone Protects an Endothelial Cell Line from H2O2 Damage.

Authors:  Bingxiang Wang; Qian Zhang; Ruyong Yao; Xiangping Liu; Zhiqiang Qu
Journal:  PLoS One       Date:  2015-08-12       Impact factor: 3.240

7.  Oxytocin receptor variant rs53576 genotype is associated with dysphoric arousal symptoms of DSM-5 posttraumatic stress disorder in Chinese earthquake survivors.

Authors:  Cheng-Qi Cao; Li Wang; Ruo-Jiao Fang; Gen Li; Ping Liu; Shu Luo; Xiang-Yang Zhang
Journal:  Chin J Traumatol       Date:  2021-03-28
  7 in total

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