Literature DB >> 31780530

Median raphe controls acquisition of negative experience in the mouse.

András Szőnyi1, Krisztián Zichó1, Albert M Barth1, Roland T Gönczi1, Dániel Schlingloff1,2, Bibiána Török2,3, Eszter Sipos3, Abel Major1, Zsuzsanna Bardóczi1, Katalin E Sos1,2, Attila I Gulyás1, Viktor Varga1, Dóra Zelena3, Tamás F Freund1, Gábor Nyiri4.   

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.
Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

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Year:  2019        PMID: 31780530     DOI: 10.1126/science.aay8746

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


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