Evidence map›Paper›PMID 21957165›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2011

Evidence for the role of hindbrain orexin-1 receptors in the control of meal size.

Eric M Parise, Nicole Lilly, Kristen Kay, Amanda M Dossat, Rohit Seth, J Michael Overton, Diana L Williams

Abstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Endocannabinoids in Body Weight Control.Pharmaceuticals (Basel, Switzerland) · 2018
    Review
  10. Review
  11. Ventral tegmental area orexin 1 receptors promote palatable food intake and oppose postingestive negative feedback.American journal of physiology. Regulatory, integrative and comparative physiology · 2016
    Article
  12. Review
  13. Computational Analysis of the Hypothalamic Control of Food Intake.Frontiers in computational neuroscience · 2016
    Article
  14. Article
  15. Orexin-A enhances feeding in male rats by activating hindbrain catecholamine neurons.American journal of physiology. Regulatory, integrative and comparative physiology · 2015
    Article
  16. Article
  17. Review
  18. Article
  19. 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

7 authors at 1 institution in 1 country.

Eric M PariseDepartment of Psychology and Program in Neuroscience, Florida State University, Tallahassee, Florida 32306-4301, USA.
Nicole Lilly
Kristen Kay
Amanda M Dossat
Rohit Seth
J Michael Overton
Diana L Williams
Florida State University · US

Funding

Brain integration of adiposity and satiety signals in the control of food intakeR00DK078779 · NIDDK · FLORIDA STATE UNIVERSITY · PI WILLIAMS, DIANA L · 2009 to 2011
$747k
NIDDK NIH HHS DK-078779
6 · The paper itself

Abstract

Hypothalamic orexin neurons project to the hindbrain, and 4th-ventricle intracerebroventricular (4th-icv) injection of orexin-A treatment increases food intake. We assessed the effects of hindbrain orexin-A and the orexin-1-receptor antagonist SB334867 on meal pattern in rats consuming standard chow. When injected 4th-icv shortly before dark onset, lower doses of orexin-A increased food intake over a 2-h period by increasing the size of the first meal relative to vehicle, whereas the highest dose increased food intake by causing the second meal to be taken sooner. Conversely, hindbrain SB334867 reduced food intake by decreasing the size of the first meal of the dark phase. We also examined the effects of 4th-icv orexin-A and SB334867 on locomotor activity. Only the highest dose of orexin-A increased activity, and SB334867 had no effect. In addition, hindbrain SB334867 induced c-Fos in the nucleus of the solitary tract. These data support the suggestion that endogenous hindbrain orexin-A acts to limit satiation. Both orexin-A and the pancreatic satiation hormone amylin require an intact area postrema to affect food intake, so we asked whether 4th-icv orexin-A impairs the satiating effect of peripheral amylin treatment. Amylin reduced the size of the first meal of the dark cycle when rats were pretreated with 4th-icv saline, yet amylin was ineffective after 4th-icv orexin-A pretreatment. Using double-label immunohistochemistry, we determined that some orexin-A fibers in the area postrema are located in proximity to amylin-responsive neurons. Therefore, hindbrain orexin-A may increase food intake, in part, by reducing the ability of rats to respond to amylin during a meal.

Indexed as

AnimalsBenzoxazolesEatingIntracellular Signaling Peptides and ProteinsIslet Amyloid PolypeptideMaleMotor ActivityNaphthyridinesNeuropeptidesOrexin ReceptorsOrexinsPhotoperiodRatsRats, WistarReceptors, G-Protein-CoupledReceptors, Neuropeptide1-(2-methylbenzoxazol-6-yl)-3-(1,5)naphthyridin-4-yl ureaBenzoxazolesIntracellular Signaling Peptides and ProteinsIslet Amyloid PolypeptideNaphthyridinesNeuropeptidesOrexin ReceptorsOrexinsReceptors, G-Protein-CoupledReceptors, NeuropeptideUrea

Identifiers

PMID21957165
PMCPMC3233858
OpenAlexW2125965559

What OpenQuestion holds

Textmetadata
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.