Mechanism of antidepressant action of ketamine and differences between its two enantiomers.
Junbiao Zhan, Yuxi Zhang, Hao Tian, Xizi Zhu, Manlin Guo, Zhen Qiu, Zhongyuan Xia
Journal of anesthesia and translational medicine September 1, 2025 DOI: 10.1016/j.jatmed.2025.06.001 via PubMed
Summary
AI-generated from the abstractKetamine, a racemate of S-ketamine and R-ketamine, produces rapid and sustained antidepressant effects in rodent models and patients with treatment-resistant depression at subanesthetic doses. Its mechanisms involve glutamate receptors (NMDAR, AMPAR, mGluR5), molecular pathways (mTOR, ERK-CREB, PI3K/Akt), metabolites, opioid receptors, inflammation, and monoamines. S-ketamine has received FDA approval as a novel antidepressant. In rodent depression models (forced swimming test, novelty suppressed feeding, chronic social defeat stress, learned helplessness), R-ketamine showed more potent and prolonged effects without psychotomimetic side effects or abuse potential, though its clinical effects remain unclear. This review overviews ketamine's antidepressant mechanisms and differences between the two enantiomers.
Study at a glance
| Characteristics | Review Peer reviewed |
|---|---|
| Topics | Esketamine Ketamine |
| Keywords | Antidepressant effects |
| Key finding | R-ketamine shows more potent and prolonged antidepressant effects than S-ketamine in rodent models, without psychotomimetic side effects or abuse potential, but its clinical effects remain unclear. |
Abstract
Ketamine has been widely used since its discovery, and in addition to its anesthetic effects, in recent years it has been found to exhibit rapid and sustained antidepressant effects in rodent models and in patients with treatment-resistant depression (TRD) at subanesthetic doses. The antidepressant mechanism of ketamine has also been intensively studied, involving glutamate receptors such as NMDAR, AMPAR, mGluR5, molecular pathways such as mTOR, ERK-CREB, PI3K/Akt, metabolites, and other related pathways such as opioid receptors, inflammation, and monoamines. Ketamine is a racemate containing equal amounts of S-ketamine and R-ketamine. S-ketamine has recently been approved by the U.S. Food and Drug Administration (FDA) as an antidepressant with a novel mechanism of action. In rodent models of depression, such as the forced swimming test (FST), the novelty suppressed feeding (NSF) test, the chronic social defeat stress (CSDS) and the learned helplessness (LH) test, R-ketamine showed more potent and prolonged antidepressant effects. Moreover, R-ketamine was free of psychotomimetic side effects and abuse tendencies, but its clinical effects are still unclear. The enantiomers of ketamine have been known to have pharmacological and clinical differences since the late 1970s and have been studied further. The exploration of the two enantiomers of ketamine for antidepressant effects may lead to a deeper understanding of new antidepressant ideas, and this review provides an overview of the mechanism of ketamine's antidepressant action in recent years as well as the differences in the effects of the two enantiomers.