Evidence map›Paper›PMID 38236776›Full record

ArticleCell reports2024

Sympathetic NPY controls glucose homeostasis, cold tolerance, and cardiovascular functions in mice.

Raniki Kumari, Raluca Pascalau, Hui Wang, Sheetal Bajpayi, Maria Yurgel, Kwaku Quansah, Samer Hattar, Emmanouil Tampakakis, Rejji Kuruvilla

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
7.2field-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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
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  12. Advances in Adipose Tissue Biology.Endocrine reviews · 2026
    Review
  13. Review
  14. Neuropeptides and the Autonomic Nervous System in Prader-Willi Syndrome.International journal of molecular sciences · 2025
    Review
  15. Article
  16. Review
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  18. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Raniki KumariDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Raluca PascalauDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
Hui WangSection on Light and Circadian Rhythms, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA.
Sheetal BajpayiDivision of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.
Maria YurgelSection on Light and Circadian Rhythms, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA.
Kwaku QuansahDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA; Division of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.
Samer HattarSection on Light and Circadian Rhythms, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA.
Emmanouil TampakakisDivision of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.
Rejji KuruvillaDepartment of Biology, Johns Hopkins University, Baltimore, MD 21218, USA. Electronic address: rkuruvilla@jhu.edu.
Johns Hopkins University · USNational Institutes of Health · US

Funding

Neuron-satellite glia interactions in the sympathetic nervous systemR01NS133423 · NINDS · JOHNS HOPKINS UNIVERSITY · PI Rejji Kuruvilla · 2023 to 2026
$2.3M
Coupled axonal protein synthesis and lipidation in axon growth and homeostasisR01NS114478 · NINDS · JOHNS HOPKINS UNIVERSITY · PI KURUVILLA, REJJI · 2020 to 2024
$2.2M
Neurotrophic factor trafficking and signaling in development and diseaseR01NS107342 · NINDS · JOHNS HOPKINS UNIVERSITY · PI KURUVILLA, REJJI · 2019 to 2022
$1.7M
NINDS NIH HHS R01 NS107342NINDS NIH HHS R01 NS114478NINDS NIH HHS R01 NS133423
6 · The paper itself

Abstract

Neuropeptide Y (NPY) is best known for its effects in the brain as an orexigenic and anxiolytic agent and in reducing energy expenditure. NPY is also co-expressed with norepinephrine (NE) in sympathetic neurons. Although NPY is generally considered to modulate noradrenergic responses, its specific roles in autonomic physiology remain under-appreciated. Here, we show that sympathetic-derived NPY is essential for metabolic and cardiovascular regulation in mice. NPY and NE are co-expressed in 90% of prevertebral sympathetic neurons and only 43% of paravertebral neurons. NPY-expressing neurons primarily innervate blood vessels in peripheral organs. Sympathetic-specific NPY deletion elicits pronounced metabolic and cardiovascular defects in mice, including reductions in insulin secretion, glucose tolerance, cold tolerance, and pupil size and elevated heart rate, while notably, however, basal blood pressure was unchanged. These findings provide insight into target tissue-specific functions of NPY derived from sympathetic neurons and imply its potential involvement in metabolic and cardiovascular diseases.

Indexed as

Anti-Anxiety AgentsNeuropeptide YAnimalsBlood PressureGlucoseHomeostasisMiceNorepinephrineAnti-Anxiety AgentsGlucoseNeuropeptide YNorepinephrineCP: MetabolismCP: Neuroscience

Identifiers

PMID38236776
PMCPMC10951981
OpenAlexW4391035900

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.