Evidence map›Paper›PMID 29852242›Full record

ArticleNeuroscience2018

Palatable Food Affects HPA Axis Responsivity and Forebrain Neurocircuitry in an Estrous Cycle-specific Manner in Female Rats.

Ann E Egan, Abigail M K Thompson, Dana Buesing, Sarah M Fourman, Amy E B Packard, Tegesty Terefe, Dan Li, Xia Wang, Seongho Song, Matia B Solomon and 1 more

Open access · greenAbstract read
In one paragraph

Article in Neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 28% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Challenges and rewards of in vivo synaptic density imaging, and its application to the study of depression.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Eating for 3.8 × 10Frontiers in endocrinology · 2018
    Review
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

11 authors at 3 institutions in 1 country.

Ann E EganDepartment of Psychiatry and Behavioral Neuroscience, College of Medicine, University of Cincinnati, Cincinnati, OH 45237, USA.
Abigail M K ThompsonDepartment of Psychiatry and Behavioral Neuroscience, College of Medicine, University of Cincinnati, Cincinnati, OH 45237, USA.
Dana BuesingDepartment of Psychiatry and Behavioral Neuroscience, College of Medicine, University of Cincinnati, Cincinnati, OH 45237, USA.
Sarah M FourmanDepartment of Psychiatry and Behavioral Neuroscience, College of Medicine, University of Cincinnati, Cincinnati, OH 45237, USA.
Amy E B PackardDepartment of Psychiatry and Behavioral Neuroscience, College of Medicine, University of Cincinnati, Cincinnati, OH 45237, USA.
Tegesty TerefeDepartment of Psychiatry and Behavioral Neuroscience, College of Medicine, University of Cincinnati, Cincinnati, OH 45237, USA.
Dan LiAlzheimer's Therapeutic Research Institute, Keck School of Medicine, University of Southern California, San Diego, CA 92121, USA.
Xia WangDepartment of Mathematical Sciences, McMicken College of Arts and Sciences, University of Cincinnati, Cincinnati, OH 45221, USA.
Seongho SongDepartment of Mathematical Sciences, McMicken College of Arts and Sciences, University of Cincinnati, Cincinnati, OH 45221, USA.
Matia B SolomonDepartment of Psychiatry and Behavioral Neuroscience, College of Medicine, University of Cincinnati, Cincinnati, OH 45237, USA.
Yvonne M Ulrich-LaiDepartment of Psychiatry and Behavioral Neuroscience, College of Medicine, University of Cincinnati, Cincinnati, OH 45237, USA. Electronic address: yvonne.ulrich-lai@uc.edu.
University of Cincinnati Medical Center · USUniversity of Cincinnati · USAutism Research Institute · US

Funding

Lipid profile, lipoprotein and apolipoprotein composition, and intestinal fat absorption efficiency in germ-free and conventional miceU2CDK059630 · NIDDK · UNIVERSITY OF CINCINNATI · PI LIU, MIN · 2016 to 2021
$4.9M
Role of the GI lymphatic system in hormonal signaling and nutrient metabolismR01DK119135 · NIDDK · UNIVERSITY OF CINCINNATI · PI LIU, MIN, TSO, PATRICK · 2018 to 2022
$3.0M
Training Program in Neuroendocrinology of HomeostasisT32DK059803 · NIDDK · UNIVERSITY OF CINCINNATI · PI WOODS, STEPHEN C · 2001 to 2017
$2.8M
Food Reward and StressR01DK091425 · NIDDK · UNIVERSITY OF CINCINNATI · PI ULRICH-LAI, YVONNE MICHELLE · 2011 to 2015
$1.7M
FGF21 activates HPA and sympathetics via neuroinflammation and plasticityF32DK102334 · NIDDK · UNIVERSITY OF CINCINNATI · PI PACKARD, AMY ELIZABETH BRUESTLE · 2014 to 2015
$109k
NIDDK NIH HHS F32 DK102334NIDDK NIH HHS R01 DK091425NIDDK NIH HHS R01 DK119135NIDDK NIH HHS T32 DK059803NIDDK NIH HHS U2C DK059630
6 · The paper itself

Abstract

Eating palatable foods can provide stress relief, but the mechanisms by which this occurs are unclear. We previously characterized a limited sucrose intake (LSI) paradigm in which twice-daily access to a small amount of 30% sucrose (vs. water as a control) reduces hypothalamic-pituitary-adrenocortical (HPA) axis responses to stress and alters neuronal activation in stress-regulatory brain regions in male rats. However, women may be more prone to 'comfort feeding' behaviors than men, and stress-related eating may vary across the menstrual cycle. This suggests that LSI effects may be sex- and estrous cycle-dependent. The present study therefore investigated the effects of LSI on HPA axis stress responsivity, as well as markers of neuronal activation/plasticity in stress- and reward-related neurocircuitry in female rats across the estrous cycle. We found that LSI reduced post-restraint stress plasma ACTH in female rats specifically during proestrus/estrus (P/E). LSI also increased basal (non-stress) FosB/deltaFosB- and pCREB-immunolabeling in the basolateral amygdala (BLA) and central amygdala specifically during P/E. Finally, Bayesian network modeling of the FosB/deltaFosB and pCREB expression data identified a neurocircuit that includes the BLA, nucleus accumbens, prefrontal cortex, and bed nucleus of the stria terminalis as likely being modified by LSI during P/E. When considered in the context of our prior results, the present findings suggest that palatable food reduces stress responses in female rats similar to males, but in an estrous cycle-dependent manner. Further, the BLA may contribute to the LSI effects in both sexes, whereas the involvement of other brain regions appears to be sex-dependent.

Indexed as

FoodAdrenal GlandsAdrenocorticotropic HormoneAnimalsCorticosteroneEstradiolEstrous CycleFemaleHypothalamo-Hypophyseal SystemNeural PathwaysPituitary-Adrenal SystemProsencephalonRatsRats, Long-EvansRestraint, PhysicalStress, PhysiologicalAdrenocorticotropic HormoneCorticosteroneEstradiolSucroseACTHbasolateral amygdalacorticosteronenucleus accumbenssex differencessucrose

Identifiers

PMID29852242
PMCPMC6071329
OpenAlexW2805053846

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.