Literature DB >> 35296422

Duration of Reduction in Enduring Stress-Induced Hyperalgesia Via FKBP51 Inhibition Depends on Timing of Administration Relative to Traumatic Stress Exposure.

Britannia J Wanstrath1, Samuel A McLean2, Ying Zhao1, Jacqueline Mickelson1, Michael Bauder3, Felix Hausch3, Sarah D Linnstaedt4.   

Abstract

Chronic pain development is a frequent outcome of severe stressor exposure, with or without tissue injury. Enduring stress-induced hyperalgesia (ESIH) is believed to play a central role, but the precise mechanisms mediating the development of chronic post-traumatic pain, and the time-dependency of these mechanisms, remain poorly understood. Clinical and preclinical data suggest that the inhibition of FK506-binding protein 51 (FKBP51), a key stress system regulator, might prevent ESIH. We evaluated whether peritraumatic inhibition of FKBP51 in an animal model of traumatic stress exposure, the single prolonged stress (SPS) model, reversed ESIH evaluated via daily mechanical von Frey testing. FKBP51 inhibition was achieved using SAFit2, a potent and specific small molecule inhibitor of FKBP51, administered to male and female Sprague-Dawley rats via intraperitoneal injection. To assess timing effects, FKBP51 was administered at different times relative to stress (SPS) exposure. SAFit2 administration immediately after SPS produced a complete reversal in ESIH lasting >7 days. In contrast, SAFit2 administration 72 hours following SPS produced only temporary hyperalgesia reversal, and administration 120h following SPS had no effect. Similarly, animals undergoing SPS together with tissue injury (plantar incision) receiving SAFit2 immediately post-surgery developed acute hyperalgesia but recovered by 4 days and did not develop ESIH. These data suggest that: 1) FKBP51 plays an important, time-dependent role in ESIH pathogenesis, 2) time windows of opportunity may exist to prevent ESIH via FKBP51 inhibition after traumatic stress, with or without tissue injury, and 3) the use of inhibitors of specific pathways may provide new insights into chronic post-traumatic pain development. PERSPECTIVE: The current work adds to a growing body of literature indicating that FKBP51 inhibition is a highly promising potential treatment strategy for reducing hyperalgesia. In the case of post-traumatic chronic pain, we show that such a treatment strategy would be particularly impactful if administered early after traumatic stress exposure.
Copyright © 2022 United States Association for the Study of Pain, Inc. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Chronic pain; FKBP51; PTSD; SAFit2; rats; stress; tissue injury

Mesh:

Substances:

Year:  2022        PMID: 35296422      PMCID: PMC9271550          DOI: 10.1016/j.jpain.2022.02.007

Source DB:  PubMed          Journal:  J Pain        ISSN: 1526-5900            Impact factor:   5.383


  67 in total

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8.  The stress regulator FKBP51: a novel and promising druggable target for the treatment of persistent pain states across sexes.

Authors:  Maria Maiarù; Oakley B Morgan; Tianqi Mao; Michaela Breitsamer; Harry Bamber; Max Pöhlmann; Mathias V Schmidt; Gerhard Winter; Felix Hausch; Sandrine M Géranton
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9.  Phenotypic characterization of frontal cortex microglia in a rat model of post-traumatic stress disorder.

Authors:  Thomas S Cotrone; Charina B Hocog; Joseph T Ramsey; Marcus A Sanchez; Heather M Sullivan; Angus G Scrimgeour
Journal:  Brain Behav       Date:  2021-01-12       Impact factor: 2.708

Review 10.  Single-Prolonged Stress: A Review of Two Decades of Progress in a Rodent Model of Post-traumatic Stress Disorder.

Authors:  Michael J Lisieski; Andrew L Eagle; Alana C Conti; Israel Liberzon; Shane A Perrine
Journal:  Front Psychiatry       Date:  2018-05-15       Impact factor: 4.157

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