Jens Randel Nyengaard

S-Ketamine Rapidly Reverses Synaptic and Vascular Deficits of Hippocampus in Genetic Animal Model of Depression

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review


BACKGROUND: The neurovascular plasticity of hippocampus is an important theory underlying major depression. Ketamine as a novel glutamatergic antidepressant drug can induce rapid antidepressant effect within hours. In a mechanistic proof-of-this concept, we examined whether ketamine leads to an increase in synaptogenesis and vascularization within 24 hours after a single injection in a genetic rat model of depression.

METHODS: Flinders Sensitive Line (FSL) and Flinders Resistant Line (FRL) rats were given a single intraperitoneal injection of ketamine (15 mg/kg) or saline. One day later, their behavior was evaluated by a modified forced swim test. Microvessel length was evaluated with global spatial sampling and optical microscopy, whereas the number of asymmetric synapses was quantified through serial section electron microscopy by using physical disector method in CA1.stratum radiatum (CA1.SR) area of hippocampus.

RESULTS: The immobility time in the forced swim test among FSL rats with ketamine treatment was significantly lower compared with FSL rats without treatment. The number of non-perforated and perforated synapses was significantly higher in the FSL-ketamine versus the FSL-vehicle group; however, ketamine did not induce a significant increase in the number of shaft synapses. Additionally, total length of microvessels was significantly increased one day after ketamine treatment in FSL rats in the hippocampal subregions including CA1.SR.

CONCLUSION: Our findings indicate that hippocampal vascularization and synaptogenesis is co-regulated rapidly after ketamine and microvascular elongation may be a supportive factor for synaptic plasticity and neuronal activity. These findings go hand-in-hand with the behavioral observations, where ketamine acts as a potent antidepressant.

Original languageEnglish
JournalInternational Journal of Neuropsychopharmacology
Pages (from-to)247-256
Publication statusPublished - 2017

See relations at Aarhus University Citationformats

ID: 104609556