4.6 Review

Repeated Dosing of Ketamine in the Forced Swim Test: Are Multiple Shots Better Than One?

Journal

FRONTIERS IN PSYCHIATRY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fpsyt.2021.659052

Keywords

chronic ketamine; forced swim test; major depression; literature search; sex differences; strain differences; sustained effects; subchronic

Categories

Funding

  1. Kavli Neuroscience Innovators at University of Michigan
  2. Neuroscience Fellows at the University of Michigan
  3. Taubman Emerging Scholars Award at the University of Michiga
  4. Pritzker Neuropsychiatric Disorders Research Consortium
  5. University of Michigan Depression Center STAR Award

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The successful repurposing of ketamine as an antidepressant has significant implications for clinical psychopharmacology. Studies suggest that repeated dosing of ketamine in rodents may have prominent depression-related effects and be more effective than a single dose. Further investigation may help optimize the use of ketamine in humans with MDD.
The anesthetic drug ketamine has been successfully repurposed as an antidepressant in human subjects. This represents a breakthrough for clinical psychopharmacology, because unlike monoaminergic antidepressants, ketamine has rapid onset, including in Major Depressive Disorder (MDD) that is resistant to conventional pharmacotherapy. This rapid therapeutic onset suggests a unique mechanism of action, which continues to be investigated in reverse translational studies in rodents. A large fraction of rodent and human studies of ketamine have focused on the effects of only a single administration of ketamine, which presents a problem because MDD is typically a persistent illness that may require ongoing treatment with this drug to prevent relapse. Here we review behavioral studies in rodents that used repeated dosing of ketamine in the forced swim test (FST), with an eye toward eventual mechanistic studies. A subset of these studies carried out additional experiments with only a single injection of ketamine for comparison, and several studies used chronic psychosocial stress, where stress is a known causative factor in some cases of MDD. We find that repeated ketamine can in some cases paradoxically produce increases in immobility in the FST, especially at high doses such as 50 or 100 mg/kg. Several studies however provide evidence that repeated dosing is more effective than a single dose at decreasing immobility, including behavioral effects that last longer. Collectively, this growing literature suggests that repeated dosing of ketamine has prominent depression-related effects in rodents, and further investigation may help optimize the use of this drug in humans experiencing MDD.

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