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Ketamine blocks a taste recognition memory in fetal rats
G A Mickley1, D R Remmers-Roeber, C Crouse
1Department of Psychology, Baldwin-Wallace College, Carnegie Hall, 275 Eastland Road, Berea, OH 44017-2088, USA. amickley@bw.edu
Pharmacology, Biochemistry, and Behavior
|February 13, 2001
Summary
NMDA receptor blockade in utero disrupts early taste recognition memory in rat pups. Fetuses exposed to ketamine showed no memory of saccharin, unlike controls.
Area of Science:
- Neuroscience
- Developmental Biology
- Behavioral Science
Background:
- Novelty/familiarity decisions are crucial for information processing and memory formation.
- Previous studies show fetal rats (E19) can form taste recognition memory for saccharin (SAC), retained until postnatal day 3 (P3).
Purpose of the Study:
- To investigate the role of N-methyl-D-aspartate (NMDA) receptors in establishing early taste recognition memory in rats.
- To determine if NMDA receptor antagonism during fetal development affects the formation or retention of taste memory.
Main Methods:
- Pregnant rats were administered ketamine (an NMDA receptor antagonist) at varying doses.
- E19 fetuses received in utero oral administration of saccharin (SAC) or water.
- Postnatal pups were tested for taste recognition memory by oral lavage with SAC and motor responses were recorded.
Main Results:
- Control neonates exhibited significantly more perseverative mouth movements, total mouth movements, and licks when tasting familiar SAC compared to novel SAC.
- This taste recognition memory response was absent in rat pups exposed to ketamine in utero.
- NMDA receptor blockade in fetuses prevented the development of the observed taste memory response.
Conclusions:
- Early non-associative taste memories in rats may be disrupted by NMDA receptor blockade during fetal development.
- NMDA receptors play a critical role in the establishment of early taste recognition memory.
- In utero exposure to NMDA receptor antagonists can impair the development of memory systems.