Ketamine differentially affects implicit and explicit memory processes in rats.
Bahar Yuksel, Zeynep Sen, Gunes Unal
Psychopharmacology June 1, 2025 DOI: 10.1007/s00213-024-06720-8 via PubMed
Summary
AI-generated from the abstractA single antidepressant dose of ketamine (10 mg/kg) given to adult Wistar rats partially impaired fear extinction when administered before fear acquisition or retrieval, but did not affect encoding or retrieval of cued fear or spatial memory. In the Morris Water Maze, ketamine facilitated memory modulation and reduced escape latency during the first day of reversal training when given before training or reversal sessions. The drug did not impair acquisition or retrieval processes in either implicit (fear) or explicit (spatial) memory tasks, but exerted opposing effects on memory modulation: disrupting fear extinction while facilitating reversal spatial learning.
Study at a glance
| Characteristics | Experimental study Peer reviewed |
|---|---|
| Population | Adult Wistar rats |
| Intervention | Ketamine |
| Dose | 10 mg/kg, IP |
| Topics | Ketamine |
| Keywords | Explicit memory Fear conditioning Implicit memory Morris water maze |
| Citations | 2 |
| Key finding | Ketamine at an antidepressant dose partially impairs fear extinction but facilitates reversal spatial learning, without affecting encoding or retrieval of cued fear or spatial memory. |
Abstract
Ketamine, a non-competitive NMDA receptor antagonist, produces antidepressant effects at subanesthetic doses. The therapeutic effect, however, is often accompanied by cognitive side effects, including memory impairments. Yet, the specific effects of ketamine on different processes of implicit and explicit memory remain to be elucidated. We examined the effect of an antidepressant dose of ketamine (10 mg/kg, IP) on the encoding, retrieval, and modulation processes of fear memory and spatial memory in adult Wistar rats. Ketamine was administered before the fear acquisition, retrieval, or extinction procedures in a Pavlovian fear conditioning task. In another set of experiments, it was administered before the training, probe trial, or reversal training phases of the Morris Water Maze (MWM). The antidepressant dose of ketamine partially impaired fear extinction when administered before the acquisition or retrieval. In contrast, it facilitated memory modulation and decreased the escape latency in the first day of reversal training in the MWM when administered before the training or reversal training sessions. Encoding or retrieval performance in either type of memory was not affected. These findings show that ketamine does not impair the acquisition or retrieval processes of cued fear or spatial memory; but exerts differential effects on memory modulation of these implicit and explicit memory paradigms, by disrupting fear extinction and facilitating reversal spatial learning.