Evidence map›Paper›PMID 27965205›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2017

Postnatal treatment with metyrapone attenuates the effects of diet-induced obesity in female rats exposed to early-life stress.

Margaret O Murphy, Joseph B Herald, Caleb T Wills, Stanley G Unfried, Dianne M Cohn, Analia S Loria

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 4% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Guidelines for in vivo models of developmental programming of cardiovascular disease risk.American journal of physiology. Heart and circulatory physiology · 2024
    Review
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  17. Maternal separation enhances anticontractile perivascular adipose tissue function in male rats on a high-fat diet.American journal of physiology. Regulatory, integrative and comparative physiology · 2018
    Article
  18. Article
  19. Sex-specific effects of stress on metabolic and cardiovascular disease: are women at higher risk?American journal of physiology. Regulatory, integrative and comparative physiology · 2017
    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 at 1 institution in 1 country.

Margaret O MurphyDepartment of Pharmacology and Nutritional Sciences, University of Kentucky, Lexington, Kentucky.
Joseph B HeraldDepartment of Pharmacology and Nutritional Sciences, University of Kentucky, Lexington, Kentucky.
Caleb T WillsDepartment of Pharmacology and Nutritional Sciences, University of Kentucky, Lexington, Kentucky.
Stanley G UnfriedDepartment of Pharmacology and Nutritional Sciences, University of Kentucky, Lexington, Kentucky.
Dianne M CohnDepartment of Pharmacology and Nutritional Sciences, University of Kentucky, Lexington, Kentucky.
Analia S LoriaDepartment of Pharmacology and Nutritional Sciences, University of Kentucky, Lexington, Kentucky analia.loria@uky.edu.
University of Kentucky · US

Funding

The role of IKKß in linking obesity to adipose tissue inflammation and adipogeneP20GM103527 · NIGMS · UNIVERSITY OF KENTUCKY · PI MORRIS, ANDREW J · 2012 to 2017
$13.7M
Early Life Stress & Chronic Control of Blood PressureR00HL111354 · NHLBI · UNIVERSITY OF KENTUCKY · PI LORIA, ANALIA · 2013 to 2015
$730k
NHLBI NIH HHS R00 HL111354NIGMS NIH HHS P20 GM103527
6 · The paper itself

Abstract

Experimental studies in rodents have shown that females are more susceptible to exhibiting fat expansion and metabolic disease compared with males in several models of fetal programming. This study tested the hypothesis that female rat pups exposed to maternal separation (MatSep), a model of early-life stress, display an exacerbated response to diet-induced obesity compared with male rats. Also, we tested whether the postnatal treatment with metyrapone (MTP), a corticosterone synthase inhibitor, would attenuate this phenotype. MatSep was performed in WKY offspring by separation from the dam (3 h/day, postnatal days 2-14). Upon weaning, male and female rats were placed on a normal (ND; 18% kcal fat) or high-fat diet (HFD; 60% kcal fat). Nondisturbed littermates served as controls. In male rats, no diet-induced differences in body weight (BW), glucose tolerance, and fat tissue weight and morphology were found between MatSep and control male rats. However, female MatSep rats displayed increased BW gain, fat pad weights, and glucose intolerance compared with control rats (P < 0.05). Also, HFD increased plasma corticosterone (196 ± 51 vs. 79 ± 18 pg/ml, P < 0.05) and leptin levels (1.8 ± 0.4 vs. 1.3 ± 0.1 ng/ml, P < 0.05) in female MatSep compared with control rats, whereas insulin and adiponectin levels were similar between groups. Female control and MatSep offspring were treated with MTP (50 µg/g ip) 30 min before the daily separation. MTP treatment significantly attenuated diet-induced obesity risk factors, including elevated adiposity, hyperleptinemia, and glucose intolerance. These findings show that exposure to stress hormones during early life could be a key event to enhance diet-induced obesity and metabolic disease in female rats. Thus, pharmacological and/or behavioral inflection of the stress levels is a potential therapeutic approach for prevention of early life stress-enhanced obesity and metabolic disease.

Indexed as

AnimalsAnimals, NewbornDiet, High-FatFemaleMaleMaternal DeprivationMetyraponeObesityPregnancyRatsRats, Inbred WKYStress, PsychologicalWeight GainMetyraponeearly-life stresshigh fat dietmaternal separationmetyraponesex differences in developmental programming of metabolic disease

Identifiers

PMID27965205
PMCPMC5336565
OpenAlexW2561320737

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.