Ketamine sex- and dose-dependently mitigates behavioral sequelae induced by a predator-based psychosocial stress model of post-traumatic stress disorder

Current pharmacotherapy for post-traumatic stress disorder (PTSD), a debilitating psychiatric condition that develops in a subset of traumatized individuals, is inadequate. Over the past two decades, numerous studies have shown that ketamine, a non-competitive NMDA receptor antagonist, exerts rapid...

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Veröffentlicht in:Behavioural brain research 2022-06, Vol.428, p.113895-113895, Article 113895
Hauptverfasser: Zoladz, Phillip R., Del Valle, Colin R., Goodman, Cassandra S., Dodson, Jordan L., Smith, Ian F., Elmouhawesse, Kara M., Sparkman, Heather R., Naylor, Margaret M., Hopson, Elizabeth P.
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Sprache:eng
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Zusammenfassung:Current pharmacotherapy for post-traumatic stress disorder (PTSD), a debilitating psychiatric condition that develops in a subset of traumatized individuals, is inadequate. Over the past two decades, numerous studies have shown that ketamine, a non-competitive NMDA receptor antagonist, exerts rapid antidepressant effects in both humans and rodents, but the anxiolytic profile of ketamine, as well as its ability to treat PTSD-related symptoms, is still unclear. Thus, we examined the ability of a single administration of ketamine to prevent the onset of PTSD-like sequelae in a chronic psychosocial stress model of PTSD. Adult male and female Sprague-Dawley rats were exposed to a cat on two occasions, in combination with chronic social instability. Immediately following the cat exposure on Day 1, rats were given intraperitoneal injections of 10 mg/kg or 15 mg/kg ketamine or vehicle; control rats were injected with vehicle. Three weeks after the second cat exposure, we assessed symptoms of hyperarousal and anxiety-like behavior in the rats. In males, chronic stress led to greater anxiety on the elevated plus maze and in the open field; in females, chronic stress resulted in an exaggerated startle response and greater anxiety in the open field. These effects were most effectively prevented by the administration of 10 mg/kg ketamine. These findings demonstrate that ketamine can prophylactically prevent the onset of PTSD-like behaviors in males and females. Their sex-dependent nature is consistent with previous preclinical research and highlights the need for future research to examine their neurobiological basis. •Single injection of ketamine prevented PTSD-like sequelae in male and female rats.•In males, stress increased anxiety on the plus maze and in the open field.•In females, stress increased anxiety in the open field and led to hyperarousal.•10 mg/kg ketamine was most effective in preventing stressed effects in both sexes.
ISSN:0166-4328
1872-7549
DOI:10.1016/j.bbr.2022.113895