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Lack of metabolism in (R)-ketamine's antidepressant actions in a chronic social defeat stress model.

Kai Zhang, Yuko Fujita, Kenji Hashimoto

Scientific Reports March 5, 2018 DOI: 10.1038/s41598-018-22449-9 (opens in new tab)

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Study at a glance

AI-extracted from the abstract
Characteristics Preclinical pharmacokinetic and behavioral study Peer reviewed
Population Rodents (chronic social defeat stress model of depression)
Interventions (R)-ketamine (2R 6R)-hydroxynorketamine (HNK)
Duration 7 days (antidepressant effect follow-up)
Topics Esketamine Ketamine
Key points A single intracerebroventricular infusion of (R)-ketamine showed rapid and long-lasting (7 days) antidepressant effects in a chronic social defeat stress model, whereas (2R,6R)-HNK infusion showed no antidepressant effect despite higher brain concentrations. The authors argue it is unlikely that (2R,6R)-HNK is essential for the antidepressant actions of (R)-ketamine in this model.

Abstract

Since the metabolism of (R,S)-ketamine to (2R,6R)-hydroxynorketamine (HNK) is reported to be essential for ketamine's antidepressant effects, there is an increasing debate about antidepressant effects of (2R,6R)-HNK. Using pharmacokinetic and behavioral techniques, we investigated whether intracerebroventricular (i.c.v.) infusion of (R)-ketamine or (2R,6R)-HNK show antidepressant effects in a chronic social defeat stress (CSDS) model of depression. Low levels of (2R,6R)-HNK in the brain after i.c.v. infusion of (R)-ketamine were detected, although brain levels of (2R,6R)-HNK were markedly lower than those after i.c.v. infusion of (2R,6R)-HNK. Furthermore, high levels of (2R,6R)-HNK in the blood and liver after i.c.v. infusion of (R)-ketamine or (2R,6R)-HNK were detected. A single i.c.v. infusion of (R)-ketamine showed rapid and long-lasting (7 days) antidepressant effects in a CSDS model. In contrast, i.c.v. infusion of (2R,6R)-HNK did not show any antidepressant effect in the same model, although brain concentration of (2R,6R)-HNK was higher than after i.c.v. infusion of (R)-ketamine. This study suggest that (R)-ketamine in the periphery after washout from the brain is metabolized to (2R,6R)-HNK in the liver, and subsequently, (2R,6R)-HNK enters into brain tissues. Furthermore, it is unlikely that (2R,6R)-HNK is essential for the antidepressant actions of (R)-ketamine in a CSDS model.

Comparable studies

Other preclinical and animal studies on ketamine, most cited first.

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