Abstract
The paradigmatic feature of long-term memory (LTM) is its persistence. However, little is known about the mechanisms that make some LTMs last longer than others. In rats, a long-lasting fear LTM vanished rapidly when the D1 dopamine receptor antagonist SCH23390 was injected into the dorsal hippocampus 12 hours, but not immediately or 9 hours, after the fearful experience. Conversely, intrahippocampal application of the D1 agonist SK38393 at the same critical post-training time converted a rapidly decaying fear LTM into a persistent one. This effect was mediated by brain-derived neurotrophic factor and regulated by the ventral tegmental area (VTA). Thus, the persistence of LTM depends on activation of VTA/hippocampus dopaminergic connections and can be specifically modulated by manipulating this system at definite post-learning time points.
Original language | English |
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Pages (from-to) | 1017-1020 |
Number of pages | 4 |
Journal | Science |
Volume | 325 |
Issue number | 5943 |
DOIs | |
Publication status | Published - 21 Aug 2009 |
Keywords
- VENTRAL TEGMENTAL AREA
- HIPPOCAMPAL SLICES
- CA1 REGION
- NEURONS
- RECEPTORS
- RAT
- LTP
- POTENTIATION
- INFORMATION
- ACTIVATION