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Ketamine retards recovery from reward downshift and supports conditioned taste aversion.

Antonio D R Agüera, Clara Cándido, Rocío Donaire, Mauricio R Papini, Carmen Torres

Pharmacology, biochemistry, and behavior October 28, 2023 DOI: 10.1016/j.pbb.2023.173671 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Experimental study Peer reviewed
Population Food-restricted male rats
Intervention Ketamine
Dose 10 mg/kg, ip
Duration 10 preshift sessions followed by 4 postshift sessions (each 5-min access); injections on sessions 11 and 12 or immediately after session 11
Topics Ketamine Esketamine
Keywords Conditioned taste aversion Frustration Motivational summation Reward downshift Ketamine effects ketamine Drug effects Pharmacology Reinforcement Emotional memory
Citations 4
Key findings Ketamine increased consummatory suppression in rats experiencing unexpected reward downshift and induced conditioned taste aversion to 4% sucrose even without reward downshift.

Abstract

Ketamine is a noncompetitive N-methyl-d-aspartate (NMDA) receptor antagonist with antidepressant, anxiolytic, and memory effects in clinical and preclinical studies. The present studies investigated the behavioral effects of ketamine in animals exposed to a consummatory successive negative contrast (cSNC) task involving unexpected reward downshift, negative emotion (frustration), and aversive memory. Food-restricted male rats had 5-min access to 32 % sucrose in each of 10 preshift sessions followed by 4 % sucrose in 4 postshift sessions. Unshifted controls had access to 4 % sucrose during all 14 sessions. Ketamine (10 mg/kg, ip) was injected 30 min before sessions 11 and 12 (Experiment 1) or immediately after session 11 (Experiment 3). The results showed that both pre- and postdownshift session injection of ketamine increased consummatory suppression, as Group 32/Ket exhibited lower sucrose intake than Groups 32/Sal, 4/Ket, and 4/Sal. These effects extended beyond the day(s) of injection. Experiments 2 and 4 showed that the same dose, route of administration, and time of injection induced significant conditioned taste aversion to 4 % sucrose, in the absence of reward downshift. These data suggest that ketamine induces an aversive state that may summate with frustration induced by reward downshift in the cSNC task and also support a conditioned taste aversion to 4 % sucrose in the absence of reward downshift. Implications for these and other experiments involving pre- and postsession administration of ketamine are discussed.

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