Evidence map›Paper›PMID 28708877›Full record

ArticlePloS one2017

Median raphe region stimulation alone generates remote, but not recent fear memory traces.

Diána G Balázsfi, Dóra Zelena, Lívia Farkas, Kornél Demeter, István Barna, Csaba Cserép, Virág T Takács, Gábor Nyíri, Flóra Gölöncsér, Beáta Sperlágh and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 23 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Diána G BalázsfiDepartment of Behavioral Neurobiology, Institute of Experimental Medicine, Budapest, Hungary.ORCID http://orcid.org/0000-0003-1373-7848
Dóra ZelenaDepartment of Behavioral Neurobiology, Institute of Experimental Medicine, Budapest, Hungary.
Lívia FarkasDepartment of Behavioral Neurobiology, Institute of Experimental Medicine, Budapest, Hungary.
Kornél DemeterDepartment of Behavioral Neurobiology, Institute of Experimental Medicine, Budapest, Hungary.
István BarnaDepartment of Behavioral Neurobiology, Institute of Experimental Medicine, Budapest, Hungary.
Csaba CserépDepartment of Cellular and Network Neurobiology, Institute of Experimental Medicine, Budapest, Hungary.
Virág T TakácsDepartment of Cellular and Network Neurobiology, Institute of Experimental Medicine, Budapest, Hungary.
Gábor NyíriDepartment of Cellular and Network Neurobiology, Institute of Experimental Medicine, Budapest, Hungary.
Flóra GölöncsérDepartment of Pharmacology, Institute of Experimental Medicine, Budapest, Hungary.
Beáta SperlághDepartment of Pharmacology, Institute of Experimental Medicine, Budapest, Hungary.
Tamás F FreundDepartment of Cellular and Network Neurobiology, Institute of Experimental Medicine, Budapest, Hungary.
József HallerDepartment of Behavioral Neurobiology, Institute of Experimental Medicine, Budapest, Hungary.
HUN-REN Institute of Experimental Medicine · HUSemmelweis University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The median raphe region (MRR) is believed to control the fear circuitry indirectly, by influencing the encoding and retrieval of fear memories by amygdala, hippocampus and prefrontal cortex. Here we show that in addition to this established role, MRR stimulation may alone elicit the emergence of remote but not recent fear memories. We substituted electric shocks with optic stimulation of MRR in C57BL/6N male mice in an optogenetic conditioning paradigm and found that stimulations produced agitation, but not fear, during the conditioning trial. Contextual fear, reflected by freezing was not present the next day, but appeared after a 7 days incubation. The optogenetic silencing of MRR during electric shocks ameliorated conditioned fear also seven, but not one day after conditioning. The optogenetic stimulation patterns (50Hz theta burst and 20Hz) used in our tests elicited serotonin release in vitro and lead to activation primarily in the periaqueductal gray examined by c-Fos immunohistochemistry. Earlier studies demonstrated that fear can be induced acutely by stimulation of several subcortical centers, which, however, do not generate persistent fear memories. Here we show that the MRR also elicits fear, but this develops slowly over time, likely by plastic changes induced by the area and its connections. These findings assign a specific role to the MRR in fear learning. Particularly, we suggest that this area is responsible for the durable sensitization of fear circuits towards aversive contexts, and by this, it contributes to the persistence of fear memories. This suggests the existence a bottom-up control of fear circuits by the MRR, which complements the top-down control exerted by the medial prefrontal cortex.

Indexed as

AnimalsBehavior, AnimalBrainElectroshockFearHalorhodopsinsImmunohistochemistryMaleMemoryMiceMice, Inbred C57BLPeriaqueductal GrayProto-Oncogene Proteins c-fosSerotoninVideo RecordingHalorhodopsinsProto-Oncogene Proteins c-fosSerotonin

Identifiers

PMID28708877
PMCPMC5510848
OpenAlexW2736108724

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.