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Bedtime doses of prazosin do not affect daytime salivary amylase markers in PTSD

  • William Vaughn McCall
  • , Anilkumar Pillai
  • , Chirayu D. Pandya
  • , Laryssa McCloud
  • , Jason A. Moraczewski
  • , Liniya Tauhidul
  • , Nagy A. Youssef
  • , Doug Case
  • , Peter B. Rosenquist

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Overactivity of the noradrenergic (NE) system within the central nervous system (CNS) has been postulated as a key pathophysiology of posttraumatic stress disorder (PTSD). The activity of the enzyme salivary α-amylase (sAA) has been proposed as an indirect measure of CNS NE activity, and sAA is elevated in PTSD. As an antagonist of the α-1 NE receptor, prazosin would be expected to alter sAA values in PTSD patients. However, given its short half-life, it is not clear whether bedtime doses would have an effect on daytime sAA. In the present study, we assayed daytime sAA in 20 suicidal PTSD patients who were randomized to prazosin versus placebo at bedtime-only, and found no effect in daytime sAA. These findings are consistent with studies showing an advantage for twice daily dosing of prazosin in PTSD.

Original languageEnglish
Article numbere01709
JournalHeliyon
Volume5
Issue number5
DOIs
StatePublished - May 2019

Bibliographical note

Publisher Copyright:
© 2019

Funding

This project was supported by the American Foundation for Suicide Prevention ; DIG-0-087-13 .

FundersFunder number
American Foundation for Suicide PreventionDIG-0-087-13

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Psychiatry

    ASJC Scopus subject areas

    • General

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