Evidence map›Paper›PMID 32544386›Full record

ArticleNeuron2020

Wireless Optogenetic Stimulation of Oxytocin Neurons in a Semi-natural Setup Dynamically Elevates Both Pro-social and Agonistic Behaviors.

Sergey Anpilov, Yair Shemesh, Noa Eren, Hala Harony-Nicolas, Asaf Benjamin, Julien Dine, Vinícius E M Oliveira, Oren Forkosh, Stoyo Karamihalev, Rosa-Eva Hüttl and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Neuron, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
12.3field-weighted citation impact, top 1% 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

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 89 citations in OpenAlex.

  1. Pooled it
  2. Oxytocin selectively biases sensory-prefrontal communication through network-level suppression and theta coupling.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Primate neuroethology: a new synthesis.Trends in cognitive sciences · 2026
    Review
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  8. Article
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  14. Acute, chronic and conditioned effects of intranasal oxytocin in the mu-opioid receptor knockout mouse model of autism: Social context matters.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 5 institutions in 2 countries.

Sergey AnpilovDepartment of Neurobiology, Weizmann Institute of Science, Rehovot 7610001, Israel; Department of Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Munich 80804, Germany.
Yair ShemeshDepartment of Neurobiology, Weizmann Institute of Science, Rehovot 7610001, Israel; Department of Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Munich 80804, Germany.
Noa ErenDepartment of Neurobiology, Weizmann Institute of Science, Rehovot 7610001, Israel; Department of Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Munich 80804, Germany.
Hala Harony-NicolasSagol Department of Neurobiology, University of Haifa, Haifa 3498838, Israel.
Asaf BenjaminDepartment of Neurobiology, Weizmann Institute of Science, Rehovot 7610001, Israel; Department of Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Munich 80804, Germany.
Julien DineDepartment of Neurobiology, Weizmann Institute of Science, Rehovot 7610001, Israel; Department of Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Munich 80804, Germany.
Vinícius E M OliveiraDepartment of Behavioural and Molecular Neurobiology, Regensburg Center of Neuroscience, University of Regensburg, Regensburg 93053, Germany.
Oren ForkoshDepartment of Neurobiology, Weizmann Institute of Science, Rehovot 7610001, Israel; Department of Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Munich 80804, Germany.
Stoyo KaramihalevDepartment of Neurobiology, Weizmann Institute of Science, Rehovot 7610001, Israel; Department of Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Munich 80804, Germany.
Rosa-Eva HüttlDepartment of Neurobiology, Weizmann Institute of Science, Rehovot 7610001, Israel; Department of Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Munich 80804, Germany.
Noa FeldmanDepartment of Neurobiology, Weizmann Institute of Science, Rehovot 7610001, Israel.
Ryan BergerDepartment of Neurobiology, Weizmann Institute of Science, Rehovot 7610001, Israel.
Avi DaganDepartment of Neurobiology, Weizmann Institute of Science, Rehovot 7610001, Israel.
Gal ChenDepartment of Neurobiology, Weizmann Institute of Science, Rehovot 7610001, Israel.
Inga D NeumannDepartment of Behavioural and Molecular Neurobiology, Regensburg Center of Neuroscience, University of Regensburg, Regensburg 93053, Germany.
Shlomo WagnerSagol Department of Neurobiology, University of Haifa, Haifa 3498838, Israel.
Ofer YizharDepartment of Neurobiology, Weizmann Institute of Science, Rehovot 7610001, Israel.
Alon ChenDepartment of Neurobiology, Weizmann Institute of Science, Rehovot 7610001, Israel; Department of Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Munich 80804, Germany. Electronic address: alon.chen@weizmann.ac.il.
Max Planck Institute of Neurobiology · DEWeizmann Institute of Science · ILUniversity of Haifa · ILUniversity of Regensburg · DEMax Planck Institute of Psychiatry · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Complex behavioral phenotyping techniques are becoming more prevalent in the field of behavioral neuroscience, and thus methods for manipulating neuronal activity must be adapted to fit into such paradigms. Here, we present a head-mounted, magnetically activated device for wireless optogenetic manipulation that is compact, simple to construct, and suitable for use in group-living mice in an enriched semi-natural arena over several days. Using this device, we demonstrate that repeated activation of oxytocin neurons in male mice can have different effects on pro-social and agonistic behaviors, depending on the social context. Our findings support the social salience hypothesis of oxytocin and emphasize the importance of the environment in the study of social neuromodulators. Our wireless optogenetic device can be easily adapted for use in a variety of behavioral paradigms, which are normally hindered by tethered light delivery or a limited environment.

Indexed as

Social BehaviorWireless TechnologyAgonistic BehaviorAnimalsBehavior, AnimalMiceNeuronsOptogeneticsOxytocinOxytocinaggressionoptogeneticsoxytocinsocial behaviorsocial saliencewireless

Identifiers

PMID32544386
PMCPMC7447984
OpenAlexW3034990995

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.