Evidence map›Paper›PMID 31836175›Full record

ArticleBiological psychiatry2020

Ghrelin and Orexin Interact to Increase Meal Size Through a Descending Hippocampus to Hindbrain Signaling Pathway.

Andrea N Suarez, Clarissa M Liu, Alyssa M Cortella, Emily E Noble, Scott E Kanoski

Open access · greenAbstract read
In one paragraph

Article in Biological psychiatry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
3.8field-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

55 citing papers in PubMed, 1 synthesis or guideline pooled it, 85 citations in OpenAlex.

  1. [Research Advancements in Gastric Capacity Intervention for Childhood and Adolescent Obesity].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2025
    Pooled it
  2. Trial
  3. Review
  4. A ventral hippocampus to nucleus accumbens pathway regulates impulsivity in male but not female rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. A ventral hippocampus to nucleus accumbens pathway regulates impulsivity.bioRxiv : the preprint server for biology · 2025
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Andrea N SuarezHuman and Evolutionary Biology Section, Department of Biological Sciences, University of Southern California, Los Angeles, California.
Clarissa M LiuNeuroscience Graduate Program, University of Southern California, Los Angeles, California.
Alyssa M CortellaHuman and Evolutionary Biology Section, Department of Biological Sciences, University of Southern California, Los Angeles, California.
Emily E NobleHuman and Evolutionary Biology Section, Department of Biological Sciences, University of Southern California, Los Angeles, California; Department of Foods and Nutrition, University of Georgia, Athens, Georgia.
Scott E KanoskiHuman and Evolutionary Biology Section, Department of Biological Sciences, University of Southern California, Los Angeles, California; Neuroscience Graduate Program, University of Southern California, Los Angeles, California. Electronic address: kanoski@usc.edu.
University of Southern California · USUniversity of Georgia · US

Funding

Higher-Order Neural Control of Food IntakeR01DK104897 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KANOSKI, SCOTT EDWARD · 2015 to 2024
$4.3M
Control of feeding behavior by melanin-concentrating hormoneR01DK118402 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Scott Edward Kanoski · 2018 to 2026
$3.2M
Melanin-concentrating hormone and the neural regulation of feedingK01DK118000 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI NOBLE, EMILY ELIZABETH · 2019 to 2023
$769k
Ventral Hippocampus Circuits Underlying Conditioned Feeding BehaviorF31DK118944 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LIU, CLARISSA · 2018 to 2020
$81k
Gut to brain pathways regulating conditioned appetitive behaviorF31DK116558 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI SUAREZ, ANDREA · 2018 to 2019
$51k
NIDDK NIH HHS F31 DK116558NIDDK NIH HHS F31 DK118944NIDDK NIH HHS K01 DK118000NIDDK NIH HHS R01 DK104897NIDDK NIH HHS R01 DK118402
6 · The paper itself

Abstract

backgroundMemory and cognitive processes influence the amount of food consumed during a meal, yet the neurobiological mechanisms mediating these effects are poorly understood. The hippocampus (HPC) has recently emerged as a brain region that integrates feeding-relevant biological signals with learning and memory processes to regulate feeding. We investigated whether the gut-derived hormone ghrelin acts in the ventral HPC (vHPC) to increase meal size through interactions with gut-derived satiation signaling.

methodsInteractions between vHPC ghrelin signaling, gut-derived satiation signaling, feeding, and interoceptive discrimination learning were assessed via rodent behavioral neuropharmacological approaches. Downstream neural pathways were identified using transsynaptic virus-based tracing strategies.

resultsvHPC ghrelin signaling counteracted the food intake-reducing effects produced by various peripheral biological satiation signals, including cholecystokinin, exendin-4 (a glucagon-like peptide-1 receptor agonist), amylin, and mechanical distension of the stomach. Furthermore, vHPC ghrelin signaling produced interoceptive cues that generalized to a perceived state of energy deficit, thereby providing a potential mechanism for the attenuation of satiation processing. Neuroanatomical tracing identified a multiorder connection from vHPC neurons to lateral hypothalamic area orexin (hypocretin)-producing neurons that project to the laterodorsal tegmental nucleus in the hindbrain. Lastly, vHPC ghrelin signaling increased spontaneous meal size via downstream orexin receptor signaling in the laterodorsal tegmental nucleus.

conclusionsvHPC ghrelin signaling increases meal size by counteracting the efficacy of various gut-derived satiation signals. These effects occur via downstream orexin signaling to the hindbrain laterodorsal tegmental nucleus, thereby highlighting a novel hippocampus-hypothalamus-hindbrain pathway regulating meal size control.

Indexed as

GhrelinHippocampusEatingOrexinsRhombencephalonSignal TransductionGhrelinOrexinsBrainstemFood intakeLateral hypothalamusObesityRewardSatiation

Identifiers

PMID31836175
PMCPMC7188579
OpenAlexW2982690548

What OpenQuestion holds

Textmetadata
LicenceTDM
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.