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Median raphe controls acquisition of negative experience in the mouse.
- Source :
-
Science (New York, N.Y.) [Science] 2019 Nov 29; Vol. 366 (6469). - Publication Year :
- 2019
-
Abstract
- Adverse events need to be quickly evaluated and memorized, yet how these processes are coordinated is poorly understood. We discovered a large population of excitatory neurons in mouse median raphe region (MRR) expressing vesicular glutamate transporter 2 (vGluT2) that received inputs from several negative experience-related brain centers, projected to the main aversion centers, and activated the septohippocampal system pivotal for learning of adverse events. These neurons were selectively activated by aversive but not rewarding stimuli. Their stimulation induced place aversion, aggression, depression-related anhedonia, and suppression of reward-seeking behavior and memory acquisition-promoting hippocampal theta oscillations. By contrast, their suppression impaired both contextual and cued fear memory formation. These results suggest that MRR vGluT2 neurons are crucial for the acquisition of negative experiences and may play a central role in depression-related mood disorders.<br /> (Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.)
- Subjects :
- Animals
Depression physiopathology
Dorsal Raphe Nucleus metabolism
Evoked Potentials physiology
Habenula physiology
Hippocampus physiology
Male
Mice
Mice, Inbred C57BL
Neurons metabolism
Optogenetics
Theta Rhythm
Vesicular Glutamate Transport Protein 2 genetics
Aggression physiology
Anhedonia physiology
Avoidance Learning physiology
Dorsal Raphe Nucleus physiology
Vesicular Glutamate Transport Protein 2 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1095-9203
- Volume :
- 366
- Issue :
- 6469
- Database :
- MEDLINE
- Journal :
- Science (New York, N.Y.)
- Publication Type :
- Academic Journal
- Accession number :
- 31780530
- Full Text :
- https://doi.org/10.1126/science.aay8746