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Ketamine for Depression, 3: Does Chirality Matter?

Chittaranjan Andrade

The Journal of Clinical Psychiatry June 27, 2017 DOI: 10.4088/jcp.17f11681 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Review Randomized Case report Peer reviewed
Population Patients with medication-refractory depression (clinical literature); animals (preclinical literature)
Intervention S-ketamine (esketamine)
Dose 0.2-0.4 mg/kg intravenous; 28-84 mg intranasal
Topics Depression Esketamine Ketamine
Citations 80
Key findings Case reports, case series, and small randomized controlled trials suggest that single or repeated intravenous infusions (0.2-0.4 mg/kg) or intranasal administrations (28-84 mg) of S-ketamine have antidepressant action in patients with medication-refractory depression, with benefits similar in magnitude to those reported with racemic ketamine. Animal data suggest potential advantages for R-ketamine over S-ketamine. The authors note that no direct comparisons between S-ketamine and either R-ketamine or racemic ketamine in depressed patients exist, so an informed choice among the enantiomers and the racemate for depression is not possible.

Abstract

Ketamine is a racemic mixture of the enantiomers R-ketamine and S-ketamine (esketamine). S-ketamine has greater analgesic and anesthetic effects than R-ketamine and is less likely to cause psychotomimetic and other adverse effects. There is therefore an emerging interest favoring the use of S-ketamine over racemic ketamine when the drug is used for analgesia or anesthesia. This article examines preclinical and clinical literature on the antidepressant properties of S-ketamine. Animal data suggest potential advantages for R-ketamine over S-ketamine. Case reports, case series, and some small randomized controlled trials suggest that single or repeated intravenous infusions (0.2-0.4 mg/kg) or intranasal administrations (28-84 mg) of S-ketamine have antidepressant action in patients with medication-refractory depression and that the observed benefits are similar in magnitude to the antidepressant benefits reported with racemic ketamine. However, there are no direct comparisons between S-ketamine and either R-ketamine or racemic ketamine in depressed patients; therefore, it is not possible to make an informed choice when considering the enantiomers and the racemate for the indication of depression.

Comparable studies

Other narrative reviews on ketamine for depression, most cited first.

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