Evidence map›Paper›PMID 38211586›Full record

ArticleCurrent biology : CB2024

The preoptic area and dorsal habenula jointly support homeostatic navigation in larval zebrafish.

Virginia Palieri, Emanuele Paoli, You Kure Wu, Martin Haesemeyer, Ilona C Grunwald Kadow, Ruben Portugues

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
8.5field-weighted citation impact, top 2% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Neural Control of Homeothermy, Torpor, and Hibernation.Annual review of neuroscience · 2026
    Review
  4. PGE2 modulation of stimulus valence directs zebrafish behavioral fever.bioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Learning to Navigate in Chemical Fields Without A Map at Low Reynolds Numbers.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Modeling of Charcot-Marie-Tooth disease in zebrafish.Frontiers in molecular neuroscience · 2025
    Review
  18. Article
  19. Review
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

6 authors at 4 institutions in 2 countries.

Virginia PalieriInstitute of Neuroscience, Technical University of Munich, Biedersteiner Strasse 29, 80802 Munich, Germany; School of Life Sciences, Technical University of Munich, Freising, Germany.
Emanuele PaoliInstitute of Neuroscience, Technical University of Munich, Biedersteiner Strasse 29, 80802 Munich, Germany.
You Kure WuInstitute of Neuroscience, Technical University of Munich, Biedersteiner Strasse 29, 80802 Munich, Germany.
Martin HaesemeyerDepartment of Neuroscience, The Ohio State University College of Medicine, Columbus, OH 43210, USA.
Ilona C Grunwald KadowSchool of Life Sciences, Technical University of Munich, Freising, Germany; Institute of Physiology II, University of Bonn, Medical Faculty (UKB), Nussallee 11, 53115 Bonn, Germany. Electronic address: ilona.grunwald@ukbonn.de.
Ruben PortuguesInstitute of Neuroscience, Technical University of Munich, Biedersteiner Strasse 29, 80802 Munich, Germany; Munich Cluster of Systems Neurology (SyNergy), Feodor-Lynen-Str. 17, 81377 Munich, Germany. Electronic address: ruben.portugues@tum.de.
Technical University of Munich · DEMunich Cluster for Systems Neurology · DEThe Ohio State University · USUniversity of Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Animals must maintain physiological processes within an optimal temperature range despite changes in their environment. Through behavioral assays, whole-brain functional imaging, and neural ablations, we show that larval zebrafish, an ectothermic vertebrate, achieves thermoregulation through homeostatic navigation-non-directional and directional movements toward the temperature closest to its physiological setpoint. A brain-wide circuit encompassing several brain regions enables this behavior. We identified the preoptic area of the hypothalamus (PoA) as a key brain structure in triggering non-directional reorientation when thermal conditions are worsening. This result shows an evolutionary conserved role of the PoA as principal thermoregulator of the brain also in ectotherms. We further show that the habenula (Hb)-interpeduncular nucleus (IPN) circuit retains a short-term memory of the sensory history to support the generation of coherent directed movements even in the absence of continuous sensory cues. We finally provide evidence that this circuit may not be exclusive for temperature but may convey a more abstract representation of relative valence of physiologically meaningful stimuli regardless of their specific identity to enable homeostatic navigation.

Indexed as

HabenulaZebrafishAnimalsBody Temperature RegulationLarvaPreoptic Areabehavioral strategydorsal habenulaectothermic vs. endothermichomeostasisinnate behaviorpreoptic areasensory contextthermoregulationvalencezebrafish

Identifiers

PMID38211586
PMCPMC10849091
OpenAlexW4390704239

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.