Efficacy of fluoxetine and (R,S)-ketamine in attenuating conditioned fear behaviors in male mice.
Megan Wells, Jan Hoffmann, Autumn Stage, Isabella Enger, Jayme Pomper, Lily Briggs, Amber LaCrosse
The Journal of pharmacology and experimental therapeutics January 1, 2025 DOI: 10.1124/jpet.124.002252 via PubMed
Summary
AI-generated from the abstractCombining a single dose of ketamine with chronic fluoxetine (Prozac) reduces fear memory in mice two weeks after fear conditioning, though it does not reduce anxiety or fear generalization in an open field test. Fluoxetine alone was most effective at reducing fear generalization. Current PTSD medications lead to symptom remission in fewer than 30% of patients. This study offers preliminary support for a more effective therapeutic option for stress-related disorders.
Study at a glance
| Characteristics | Preclinical experimental study Peer reviewed |
|---|---|
| Population | Rodents (mice) |
| Interventions | Acute (R S)-ketamine chronic fluoxetine |
| Duration | 2 weeks |
| Topics | Ketamine PTSD |
| Keywords | Conditioned fear Fluoxetine Mice |
| Citations | 1 |
| Key finding | Combined acute ketamine and chronic fluoxetine reduced fear memory during re-exposure at two weeks, but fluoxetine alone was most effective for fear generalization. |
Abstract
Post-traumatic stress disorder (PTSD) is caused by exposure to a traumatic or stressful event. Symptoms related to this disorder include persistent re-experiencing of memories and fear of generalization. Current pharmacological treatments for PTSD are insufficient, with fewer than 30% of patients reporting symptom remission. This study aims to determine the efficacy of acute (R,S)-ketamine and chronic fluoxetine (FLX) in reducing fear memory and fear generalization. In rodents, fear conditioning (FC) is commonly used in the literature to induce behaviors related to symptoms of PTSD, and the open field test (OFT) can assess anxiety and fear generalization behaviors during the exploration of a novel environment. In this study, FC consisted of a white noise cue stimulus and 4 inescapable foot shocks. Treatments began 4 hours after FC. Fear and anxiety behaviors were recorded during re-exposure to the FC stimuli at 24 hours and 2 weeks. The OFT was conducted 1 day before the last FC re-exposure. Results support the combined use of acute ketamine and chronic FLX as a treatment for reducing behaviors indicative of fear memory during re-exposure at 2 weeks, but not behaviors indicative of anxiety and fear generalization in the OFT. FLX alone was most effective in reducing behaviors related to fear generalization. This study contributes to the existing literature on pharmacological treatment for fear and anxiety behaviors relating to fear memory and fear generalization. Continued research is necessary to replicate results, optimize treatment protocols, and investigate the molecular adaptations to trauma and treatment. SIGNIFICANCE STATEMENT: Up to 6% of people in the United States will develop PTSD within their lifetime, and less than half of those individuals will find relief from their symptoms given the current therapeutic options. This study offers preliminary support for the efficacy of ketamine and FLX in reducing PTSD-like behaviors induced by fear-conditioning in mice. Compared with current standard treatments, the results of the current study indicate the potential for a more effective therapeutic option for those with stress-related disorders, such as PTSD.