Evidence map›Paper›PMID 30893297›Full record

ArticlePLoS biology2019

Lateral hypothalamic neurotensin neurons promote arousal and hyperthermia.

Fumito Naganuma, Daniel Kroeger, Sathyajit S Bandaru, Gianna Absi, Joseph C Madara, Ramalingam Vetrivelan

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

40 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Hypothalamic control of arousal.Reviews in endocrine & metabolic disorders · 2026
    Review
  3. Article
  4. Review
  5. Role of Hypothalamic CRH Neurons in Regulating the Impact of Stress on Memory and Sleep.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Distinct lateral hypothalamic CaMKIIα neuronal populations regulate wakefulness and locomotor activity.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  14. Review
  15. Article
  16. Neural Control of REM Sleep and Motor Atonia: Current Perspectives.Current neurology and neuroscience reports · 2023
    Review
  17. Review
  18. Article
  19. Structure and Function of Neuronal Circuits Linking Ventrolateral Preoptic Nucleus and Lateral Hypothalamic Area.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  20. Article
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 1 institution in 2 countries.

Fumito NaganumaDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States of America.
Daniel KroegerDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States of America.
Sathyajit S BandaruDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States of America.
Gianna AbsiDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States of America.
Joseph C MadaraDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States of America.
Ramalingam VetrivelanDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States of America.ORCID 0000-0002-6376-3641
Beth Israel Deaconess Medical Center · US

Funding

Neural mechanisms underlying REM sleep regulation by MCH neuronsR01NS088482 · NINDS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI RAMALINGAM, VETRIVELAN · 2015 to 2019
$1.9M
NINDS NIH HHS R01 NS088482
6 · The paper itself

Abstract

Sleep and wakefulness are greatly influenced by various physiological and psychological factors, but the neuronal elements responsible for organizing sleep-wake behavior in response to these factors are largely unknown. In this study, we report that a subset of neurons in the lateral hypothalamic area (LH) expressing the neuropeptide neurotensin (Nts) is critical for orchestrating sleep-wake responses to acute psychological and physiological challenges or stressors. We show that selective activation of NtsLH neurons with chemogenetic or optogenetic methods elicits rapid transitions from non-rapid eye movement (NREM) sleep to wakefulness and produces sustained arousal, higher locomotor activity (LMA), and hyperthermia, which are commonly observed after acute stress exposure. On the other hand, selective chemogenetic inhibition of NtsLH neurons attenuates the arousal, LMA, and body temperature (Tb) responses to a psychological stress (a novel environment) and augments the responses to a physiological stress (fasting).

Indexed as

AnimalsBody TemperatureElectrophoresisFeverGenotyping TechniquesHypothalamic Area, LateralLocomotionMaleMiceNeuronsNeurotensinNeurotensin

Identifiers

PMID30893297
PMCPMC6426208
OpenAlexW2923051951

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.