Literature DB >> 23438728

Non-Antidepressant Long-term Treatment in Post-Traumatic Stress Disorder (PTSD).

Hala Kerbage, Sami Richa1.   

Abstract

INTRODUCTION: Post-traumatic stress disorder (PTSD) is a frequent and disabling condition that occurs after exposure to a traumatic event, and Selective Serotonin Reuptake Inhibitors (SSRIs) are considered the first-line treatment approach for this disorder. However, a large proportion of patients remain symptomatic and other pharmacological agents have been investigated, based on the understanding of the underlying biological dysfunctions of PTSD.
METHODS: We conducted a review of the literature on the pharmacological options for PTSD other than the antidepressants, using MedLine and Web of Science databases, with search terms including the pharmacologic class of each agent plus PTSD, or pharmacotherapy, or fear conditioning. The literature review covered articles published until august 2012, including reviews and original articles.
RESULTS: Agents like antipsychotics, anticonvulsants, benzodiazepines, anti-adrenergic agents, have been studied in randomized clinical trials (RCTs), with general positive results for antipsychotics, especially as adjunct therapy, and for prazosin for sleep-related disturbances. However, one important target for novel medications is the modulation of the fear conditioning process, through the alteration of retrieval/reconsolidation or enhancement of fear extinction. This is traditionally targeted in prolonged exposure therapy, but pre-clinical findings from studies investigating agents like propanolol, clonidine, N-Methyl-D-aspartic Acid Receptor (NMDAR) compounds, 3,4-methylenedioxy-N-methylamphetamine (MDMA) and cannabinoids, indicate promising results in affecting the fear conditioning process and thus improving PTSD core symptoms. DISCUSSION: Antipsychotics can be considered a reasonable alternative option to PTSD, with the largest body of evidence for risperidone, even though larger RCTs are warranted. Prazosin is also a promising agent, especially for sleep-related disturbances, while anticonvulsants and benzodiazepines lack empirical support. However, the most promising area for pharmacotherapy in PTSD is the modulation of the fear conditioning process, through agents used in adjunct to exposure therapy. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

Entities:  

Keywords:  Adrenoreceptor antagonists; PTSD; anticonvulsants; antipsychotics; benzodiazepines; fear conditioning; pharmacotherapy

Year:  2015        PMID: 23438728     DOI: 10.2174/157488471002150723122127

Source DB:  PubMed          Journal:  Curr Clin Pharmacol        ISSN: 1574-8847


  5 in total

Review 1.  Treatment of Post-Traumatic Stress Disorders with the Alpha-1 Adrenergic Antagonist Prazosin.

Authors:  Philippe Yves Rémy Simon; Pierre-François Rousseau
Journal:  Can J Psychiatry       Date:  2016-07-19       Impact factor: 4.356

Review 2.  The Black Book of Psychotropic Dosing and Monitoring.

Authors:  Alan F Schatzberg; DeBattista Charles
Journal:  Psychopharmacol Bull       Date:  2018-01-15

3.  High ambient temperature facilitates the acquisition of 3,4-methylenedioxymethamphetamine (MDMA) self-administration.

Authors:  Shawn M Aarde; Pai-Kai Huang; Michael A Taffe
Journal:  Pharmacol Biochem Behav       Date:  2017-10-17       Impact factor: 3.533

Review 4.  Depression and psychological trauma: an overview integrating current research and specific evidence of studies in the treatment of depression in public mental health services in chile.

Authors:  Verónica Vitriol; Alfredo Cancino; Kristina Weil; Carolina Salgado; Maria Andrea Asenjo; Soledad Potthoff
Journal:  Depress Res Treat       Date:  2014-02-17

5.  Effects of stress and MDMA on hippocampal gene expression.

Authors:  Georg F Weber; Bethann N Johnson; Bryan K Yamamoto; Gary A Gudelsky
Journal:  Biomed Res Int       Date:  2014-01-09       Impact factor: 3.411

  5 in total

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