Evidence map›Paper›PMID 23487769›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Activation of the sympathetic nervous system mediates hypophagic and anxiety-like effects of CB₁ receptor blockade.

Luigi Bellocchio, Edgar Soria-Gómez, Carmelo Quarta, Mathilde Metna-Laurent, Pierre Cardinal, Elke Binder, Astrid Cannich, Anna Delamarre, Martin Häring, Mar Martín-Fontecha and 10 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07196098 (Effect of Slow Tempo Music on Anxiety Markers During Intravitreal Injection), which is not on this map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
11.6field-weighted citation impact, top 1% 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.

NCT07196098 nacompletednot on this mapstarted 2025, after this paper: background citation

Effect of Slow Tempo Music on Anxiety Markers During Intravitreal Injection: A Randomised Controlled Trial

TypeinterventionalSponsorNg Yu SiangRan2025 to 2025Enrolled144ConditionsPain, AnxietyArmsSlow tempo music
3 · Its place in the literature

Who cites it

64 citing papers in PubMed, 115 citations in OpenAlex.

  1. The Neurochemical Orchestra of the Runner's High: A Narrative Review of Neuromodulatory Mechanisms with a Focus on Endocannabinoids.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2026
    Review
  2. Genetic Tools in Rodents to Study Cannabinoid Functions.Current topics in behavioral neurosciences · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Role of the Endocannabinoid System in Fibromyalgia.Current issues in molecular biology · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. Rational Design, Synthesis, and Evaluation of Fluorescent CBPharmaceuticals (Basel, Switzerland) · 2023
    Review
  11. The Role of the Endocannabinoid System in Binge Eating Disorder.International journal of molecular sciences · 2023
    Review
  12. Article
  13. The Endocannabinoid System and Physical Exercise.International journal of molecular sciences · 2023
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Hypothalamic endocannabinoids in obesity: an old story with new challenges.Cellular and molecular life sciences : CMLS · 2021
    Review
  20. Endogenous cannabinoids are required for MC4R-mediated control of energy homeostasis.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article

4 more citing papers are in PubMed but not listed here.

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

20 authors at 9 institutions in 4 countries.

Luigi BellocchioDepartment of Biochemistry and Molecular Biology I and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas, School of Biology, Complutense University-Instituto Universitario de Investigación Neuroquímica, 28040 Madrid, Spain.
Edgar Soria-Gómez
Carmelo Quarta
Mathilde Metna-Laurent
Pierre Cardinal
Elke Binder
Astrid Cannich
Anna Delamarre
Martin Häring
Mar Martín-Fontecha
David Vega
Thierry Leste-Lasserre
Dusan Bartsch
Krisztina Monory
Beat Lutz
Francis Chaouloff
Uberto Pagotto
Manuel Guzman
Daniela Cota
Giovanni Marsicano
Neurocentre Magendie · FRBiomedical Research Networking Center on Neurodegenerative Diseases · ESInserm · FRIRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola · ITUniversity Medical Center of the Johannes Gutenberg University Mainz · DECentral Institute of Mental Health · DEJohannes Gutenberg University Mainz · DEUniversidad Complutense de Madrid · ESUniversité de Bordeaux · FR

Funding

European Research Council 260515
6 · The paper itself

Abstract

Complex interactions between periphery and the brain regulate food intake in mammals. Cannabinoid type-1 (CB1) receptor antagonists are potent hypophagic agents, but the sites where this acute action is exerted and the underlying mechanisms are not fully elucidated. To dissect the mechanisms underlying the hypophagic effect of CB1 receptor blockade, we combined the acute injection of the CB1 receptor antagonist rimonabant with the use of conditional CB1-knockout mice, as well as with pharmacological modulation of different central and peripheral circuits. Fasting/refeeding experiments revealed that CB1 receptor signaling in many specific brain neurons is dispensable for the acute hypophagic effects of rimonabant. CB1 receptor antagonist-induced hypophagia was fully abolished by peripheral blockade of β-adrenergic transmission, suggesting that this effect is mediated by increased activity of the sympathetic nervous system. Consistently, we found that rimonabant increases gastrointestinal metabolism via increased peripheral β-adrenergic receptor signaling in peripheral organs, including the gastrointestinal tract. Blockade of both visceral afferents and glutamatergic transmission in the nucleus tractus solitarii abolished rimonabant-induced hypophagia. Importantly, these mechanisms were specifically triggered by lipid-deprivation, revealing a nutrient-specific component acutely regulated by CB1 receptor blockade. Finally, peripheral blockade of sympathetic neurotransmission also blunted central effects of CB1 receptor blockade, such as fear responses and anxiety-like behaviors. These data demonstrate that, independently of their site of origin, important effects of CB1 receptor blockade are expressed via activation of peripheral sympathetic activity. Thus, CB1 receptors modulate bidirectional circuits between the periphery and the brain to regulate feeding and other behaviors.

Indexed as

Appetite RegulationSynaptic TransmissionAnimalsAnxietyBrainFeeding and Eating DisordersGastrointestinal TractMiceMice, KnockoutReceptor, Cannabinoid, CB1Sympathetic Nervous SystemReceptor, Cannabinoid, CB1

Identifiers

PMID23487769
PMCPMC3607008
OpenAlexW2160450279

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.