Evidence map›Paper›PMID 25711718›Full record

ArticlePhysiology & behavior2015

Metabolic consequences of chronic intermittent mild stress exposure.

Abigail K Thompson, Sarah Fourman, Amy E B Packard, Ann E Egan, Karen K Ryan, Yvonne M Ulrich-Lai

Abstract read
In one paragraph

Article in Physiology & behavior, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. The Dichotomous Effect of Chronic Stress on Obesity.Trends in endocrinology and metabolism: TEM · 2016
    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

6 authors.

Abigail K ThompsonDeparment of Psychiatry and Behavioral Neuroscience, University of Cincinnati, Cincinnati, OH 45237, USA.
Sarah FourmanDeparment of Psychiatry and Behavioral Neuroscience, University of Cincinnati, Cincinnati, OH 45237, USA.
Amy E B PackardDeparment of Psychiatry and Behavioral Neuroscience, University of Cincinnati, Cincinnati, OH 45237, USA.
Ann E EganDeparment of Psychiatry and Behavioral Neuroscience, University of Cincinnati, Cincinnati, OH 45237, USA.
Karen K RyanDepartment of Internal Medicine, University of Cincinnati, Cincinnati, OH 45237, USA.
Yvonne M Ulrich-LaiDeparment of Psychiatry and Behavioral Neuroscience, University of Cincinnati, Cincinnati, OH 45237, USA. Electronic address: yvonne.ulrich-lai@uc.edu.

Funding

PREDOCTORAL TRAINING PROGRAM IN THE NEUROSCIENCEST32NS007453 · NINDS · UNIVERSITY OF CINCINNATI · PI HERMAN, JAMES P · 1997 to 2025
$4.0M
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
CNS PPARg, stress, and cardiovascular diseaseR00HL111319 · NHLBI · UNIVERSITY OF CINCINNATI · PI RYAN, KAREN · 2014 to 2016
$749k
FGF21 activates HPA and sympathetics via neuroinflammation and plasticityF32DK102334 · NIDDK · UNIVERSITY OF CINCINNATI · PI PACKARD, AMY ELIZABETH BRUESTLE · 2014 to 2015
$109k
NHLBI NIH HHS R00 HL111319NIDDK NIH HHS F32 DK102334NIDDK NIH HHS R01 DK091425NIDDK NIH HHS T32 DK059803NINDS NIH HHS T32 NS007453NINDS NIH HHS T32NS007453
6 · The paper itself

Abstract

Chronic stress in humans has divergent effects on food intake, with some individuals reporting increased vs. decreased food intake during stress. This divergence may depend in part on stress intensity, with higher-intensity stressors preferentially promoting anorexia. Consistent with this idea, rodents given a high-intensity chronic variable stress paradigm have robustly decreased food intake and body weight gain. However, the metabolic effects of a less intense chronic stress paradigm are not clear. Thus in the present study, adult male rats were given chronic intermittent mild stress (CIMS) exposure (3 cycles, in which each cycle consists of once daily mild stress for 5 days/week for 2 weeks, followed by 2 weeks of no stress) vs. non-stress controls, combined with ongoing access to a palatable diet (PD; choice of chow, high-fat diet, 30% sucrose drink, and water) vs. control diet (chow and water). As expected, access to PD increased caloric intake, body weight gain, and adiposity, and impaired glucose tolerance. CIMS decreased body weight gain only during the first cycle of stress and did not affect body weight gain thereafter, regardless of diet. Moreover, CIMS did not alter total food intake, adiposity or glucose tolerance regardless of diet. Lastly, CIMS transiently increased high-fat diet preference in PD-fed rats during the first stress cycle. Collectively, these results suggest that CIMS has relatively modest metabolic effects that occur primarily during initial stress exposure. These results support the hypothesis that the metabolic consequences of chronic stress vary with stress intensity and/or frequency.

Indexed as

AdiposityAnalysis of VarianceAnimalsBlood GlucoseBody CompositionBody WeightDiet, High-FatEatingEnergy IntakeFood PreferencesGlucose IntoleranceMaleRatsRats, Long-EvansStress, PsychologicalSucroseBlood GlucoseSucroseChronic stressDiet choiceDiet preferenceGlucose tolerancePalatable diet

Identifiers

PMID25711718
PMCPMC4545746

What OpenQuestion holds

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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.