| Literature DB >> 31780530 |
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.Entities:
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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