Evidence map›Paper›PMID 38249128›Full record

ArticleFrontiers in behavioral neuroscience2023

Entrance-sealing behavior in the home cage: a defensive response to potential threats linked to the serotonergic system and manifestation of repetitive/stereotypic behavior in mice.

Noriko Horii-Hayashi, Kazuya Masuda, Taika Kato, Kenta Kobayashi, Ayumu Inutsuka, Miyu F Nambu, Kazumasa Z Tanaka, Koichi Inoue, Mayumi Nishi

Open access · goldAbstract read
In one paragraph

Article in Frontiers in behavioral neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
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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

9 authors at 4 institutions in 1 country.

Noriko Horii-HayashiAnatomy and Cell Biology, Department of Medicine, Nara Medical University, Kashihara, Japan.
Kazuya MasudaAnatomy and Cell Biology, Department of Medicine, Nara Medical University, Kashihara, Japan.
Taika KatoAnatomy and Cell Biology, Department of Medicine, Nara Medical University, Kashihara, Japan.
Kenta KobayashiSection of Viral Vector Development, National Institute for Physiological Sciences, Okazaki, Japan.
Ayumu InutsukaDepartment of Physiology, Jichi Medical University, Shimono, Japan.
Miyu F NambuMemory Research Unit, Okinawa Institute of Science and Technology Graduate University (OIST), Kunigami-gun, Japan.
Kazumasa Z TanakaMemory Research Unit, Okinawa Institute of Science and Technology Graduate University (OIST), Kunigami-gun, Japan.
Koichi InoueAnatomy and Cell Biology, Department of Medicine, Nara Medical University, Kashihara, Japan.
Mayumi NishiAnatomy and Cell Biology, Department of Medicine, Nara Medical University, Kashihara, Japan.
Nara Medical University · JPOkinawa Institute of Science and Technology Graduate University · JPJichi Medical University · JPNational Institute for Physiological Sciences · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The security of animal habitats, such as burrows and nests, is vital for their survival and essential activities, including eating, mating, and raising offspring. Animals instinctively exhibit defensive behaviors to protect themselves from imminent and potential threats. In 1963, researchers reported wild rats sealing the entrances to their burrows from the inside using materials such as mud, sand, and vegetation. This behavior, known as "entrance sealing (ES)," involves repetitive movements of their nose/mouth and forepaws and is likely a proactive measure against potential intruders, which enhances burrow security. These observations provide important insights into the animals' ability to anticipate potential threats that have not yet occurred and take proactive actions. However, this behavior lacks comprehensive investigation, and the neural mechanisms underpinning it remain unclear. Hypothalamic perifornical neurons expressing urocortin-3 respond to novel objects/potential threats and modulate defensive responses to the objects in mice, including risk assessment and burying. In this study, we further revealed that chemogenetic activation of these neurons elicited ES-like behavior in the home-cage. Furthermore, behavioral changes caused by activating these neurons, including manifestations of ES-like behavior, marble-burying, and risk assessment/burying of a novel object, were effectively suppressed by selective serotonin-reuptake inhibitors. The c-Fos analysis indicated that ES-like behavior was potentially mediated through GABAergic neurons in the lateral septum. These findings underscore the involvement of hypothalamic neurons in the anticipation of potential threats and proactive defense against them. The links of this security system with the manifestation of repetitive/stereotypic behaviors and the serotonergic system provide valuable insights into the mechanisms underlying the symptoms of obsessive-compulsive disorder.

Indexed as

anxietydefensive behaviorhypothalamusneuropeptideobsessive-compulsive disorderselective serotonin-reuptake inhibitorserotoninurocortin-3

Identifiers

PMID38249128
PMCPMC10799337
OpenAlexW4390610808

What OpenQuestion holds

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LicenceCC BY
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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.