Evidence map›Paper›PMID 39412856›Full record

ArticleeLife2024

Hypothalamic representation of the imminence of predator threat detected by the vomeronasal organ in mice.

Quynh Anh Thi Nguyen, Andrea Rocha, Ricky Chhor, Yuna Yamashita, Christian Stadler, Crystal Pontrello, Hongdian Yang, Sachiko Haga-Yamanaka

Abstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Hypothalamic Control of Learned Flight Induced by Threat Imminence.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  5. Review
  6. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Quynh Anh Thi NguyenNeuroscience Graduate Program, University of California, Riverside, Riverside, United States.
Andrea RochaNeuroscience Graduate Program, University of California, Riverside, Riverside, United States.
Ricky ChhorDepartment of Molecular, Cell and Systems Biology, University of California, Riverside, Riverside, United States.
Yuna YamashitaDepartment of Molecular, Cell and Systems Biology, University of California, Riverside, Riverside, United States.
Christian StadlerNeuroscience Graduate Program, University of California, Riverside, Riverside, United States.ORCID https://orcid.org/0009-0000-7622-819X
Crystal PontrelloDepartment of Molecular, Cell and Systems Biology, University of California, Riverside, Riverside, United States.
Hongdian YangNeuroscience Graduate Program, University of California, Riverside, Riverside, United States.ORCID https://orcid.org/0000-0002-5203-9519
Sachiko Haga-YamanakaNeuroscience Graduate Program, University of California, Riverside, Riverside, United States.ORCID https://orcid.org/0000-0002-4101-9889

Funding

Locus Coeruleus-Norepinephrine Modulation of Sensory Response and Tactile PerceptionR01NS107355 · NINDS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI YANG, HONGDIAN · 2019 to 2023
$1.7M
Molecular and neural mechanisms of predator cue sensationR01DC019135 · NIDCD · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI HAGA-YAMANAKA, SACHIKO · 2021 to 2025
$1.6M
NIDCD NIH HHS R01 DC019135NIDCD NIH HHS R01DC019135NINDS NIH HHS R01 NS107355U.S. Department of Education GAANN
6 · The paper itself

Abstract

Animals have the innate ability to select optimal defensive behaviors with appropriate intensity within specific contexts. The vomeronasal organ (VNO) serves as a primary sensory channel for detecting predator cues by relaying signals to the medial hypothalamic nuclei, particularly the ventromedial hypothalamus (VMH), which directly controls defensive behavioral outputs. Here, we demonstrate that cat saliva contains predator cues that signal the imminence of predator threat and modulate the intensity of freezing behavior through the VNO in mice. Cat saliva activates VNO neurons expressing the V2R-A4 subfamily of sensory receptors, and the number of VNO neurons activated in response to saliva correlates with both the freshness of saliva and the intensity of freezing behavior. Moreover, the number of VMH neurons activated by fresh, but not old, saliva positively correlates with the intensity of freezing behavior. Detailed analyses of the spatial distribution of activated neurons, as well as their overlap within the same individual mice, revealed that fresh and old saliva predominantly activate distinct neuronal populations within the VMH. Collectively, this study suggests that there is an accessory olfactory circuit in mice that is specifically tuned to time-sensitive components of cat saliva, which optimizes their defensive behavior to maximize their chance of survival according to the imminence of threat.

Indexed as

Predatory BehaviorSalivaVomeronasal OrganAnimalsCatsCuesHypothalamusMaleMiceNeuronsaccessory olfactory systemdefensive behaviorhypothalamusmouseneuroscienceolfactory processingpredator odorthreat imminence

Identifiers

PMID39412856
PMCPMC11483128

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.