Unknown

Dataset Information

0

The NMDA agonist D-cycloserine facilitates fear memory consolidation in humans.


ABSTRACT: Animal research suggests that the consolidation of fear and extinction memories depends on N-methyl D-aspartate (NMDA)-type glutamate receptors. Using a fear conditioning and extinction paradigm in healthy normal volunteers, we show that postlearning administration of the NMDA partial agonist D-cycloserine (DCS) facilitates fear memory consolidation, evidenced behaviorally by enhanced skin conductance responses, relative to placebo, for presentations of a conditioned stimulus (CS) at a memory test performed 72 h later. DCS also enhanced CS-evoked neural responses in a posterior hippocampus/collateral sulcus region and in the medial prefrontal cortex at test. Our data suggest a role for NMDA receptors in regulating fear memory consolidation in humans.

SUBMITTER: Kalisch R 

PROVIDER: S-EPMC2638747 | biostudies-literature | 2009 Jan

REPOSITORIES: biostudies-literature

altmetric image

Publications

The NMDA agonist D-cycloserine facilitates fear memory consolidation in humans.

Kalisch Raffael R   Holt Beatrice B   Petrovic Predrag P   De Martino Benedetto B   Klöppel Stefan S   Büchel Christian C   Dolan Raymond J RJ  

Cerebral cortex (New York, N.Y. : 1991) 20080513 1


Animal research suggests that the consolidation of fear and extinction memories depends on N-methyl D-aspartate (NMDA)-type glutamate receptors. Using a fear conditioning and extinction paradigm in healthy normal volunteers, we show that postlearning administration of the NMDA partial agonist D-cycloserine (DCS) facilitates fear memory consolidation, evidenced behaviorally by enhanced skin conductance responses, relative to placebo, for presentations of a conditioned stimulus (CS) at a memory te  ...[more]

Similar Datasets

| S-EPMC8481232 | biostudies-literature
| S-EPMC3828540 | biostudies-literature
2014-09-30 | E-GEOD-59072 | biostudies-arrayexpress
| S-EPMC10055528 | biostudies-literature
2014-09-30 | GSE59072 | GEO
| S-EPMC5066480 | biostudies-literature
| S-EPMC7874630 | biostudies-literature
| S-EPMC4973269 | biostudies-literature
2023-03-13 | MSV000091477 | MassIVE
| S-EPMC4321279 | biostudies-other