Evidence map›Paper›PMID 30693314›Full record

ArticleeNeuro

Postmeal Optogenetic Inhibition of Dorsal or Ventral Hippocampal Pyramidal Neurons Increases Future Intake.

Reilly Hannapel, Janavi Ramesh, Amy Ross, Ryan T LaLumiere, Aaron G Roseberry, Marise B Parent

Open access · goldAbstract read
In one paragraph

Article in eNeuro. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.7field-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

23 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. 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
  3. Article
  4. A ventral hippocampus to nucleus accumbens pathway regulates impulsivity.bioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Is there a role for higher cognitive processes in the development of obesity in humans?Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Inhibiting ventral hippocampal NMDA receptors andLearning & memory (Cold Spring Harbor, N.Y.) · 2021
    Article
  17. Article
  18. Article
  19. Review
  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 2 institutions in 1 country.

Reilly HannapelNeuroscience Institute, Georgia State University, Atlanta, GA 30303.
Janavi RameshNeuroscience Institute, Georgia State University, Atlanta, GA 30303.
Amy RossNeuroscience Institute, Georgia State University, Atlanta, GA 30303.
Ryan T LaLumiereDepartment of Psychological and Brain Sciences and Iowa Neuroscience Institute, University of Iowa, Iowa City, IA 52242.ORCID 0000-0002-1235-0521
Aaron G RoseberryNeuroscience Institute, Georgia State University, Atlanta, GA 30303.ORCID 0000-0003-0468-0333
Marise B ParentNeuroscience Institute, Georgia State University, Atlanta, GA 30303.ORCID 0000-0001-7862-5623
Georgia State University · USUniversity of Iowa · US

Funding

Neural Pathways Modulating Memory ConsolidationR01MH104384 · NIMH · UNIVERSITY OF IOWA · PI LALUMIERE, RYAN T, MCINTYRE, CHRISTA · 2015 to 2019
$1.9M
Hippocampal Modulation of Energy IntakeR01DK114700 · NIDDK · GEORGIA STATE UNIVERSITY · PI PARENT, MARISE B · 2018 to 2020
$1.5M
NIDDK NIH HHS R01 DK114700NIMH NIH HHS R01 MH104384
6 · The paper itself

Abstract

Memory of a recently eaten meal can serve as a powerful mechanism for controlling future eating behavior because it provides a record of intake that likely outlasts most physiological signals generated by the meal. In support, impairing the encoding of a meal in humans increases the amount ingested at the next eating episode. However, the brain regions that mediate the inhibitory effects of memory on future intake are unknown. In the present study, we tested the hypothesis that dorsal hippocampal (dHC) and ventral hippocampal (vHC) glutamatergic pyramidal neurons play a critical role in the inhibition of energy intake during the postprandial period by optogenetically inhibiting these neurons at specific times relative to a meal. Male Sprague Dawley rats were given viral vectors containing CaMKIIα-eArchT3.0-eYFP or CaMKIIα-GFP and fiber optic probes into dHC of one hemisphere and vHC of the other. Compared to intake on a day in which illumination was not given, inhibition of dHC or vHC glutamatergic neurons after the end of a chow, sucrose, or saccharin meal accelerated the onset of the next meal and increased the amount consumed during that next meal when the neurons were no longer inhibited. Inhibition given during a meal did not affect the amount consumed during that meal or the next one but did hasten meal initiation. These data show that dHC and vHC glutamatergic neuronal activity during the postprandial period is critical for limiting subsequent ingestion and suggest that these neurons inhibit future intake by consolidating the memory of the preceding meal.

Indexed as

AnimalsDietary SucroseEatingFeeding BehaviorGlutamic AcidHippocampusMemoryNeural InhibitionOptogeneticsPostprandial PeriodPyramidal CellsRats, Sprague-DawleySaccharinTissue Culture TechniquesDietary SucroseGlutamic AcidSaccharinfeedinghippocampusmemorypostprandialsaccharinsucrose

Identifiers

PMID30693314
PMCPMC6348449
OpenAlexW2908790444

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.