Evidence map›Paper›PMID 28101317›Full record

ArticleBiology of sex differences2017

Corticotropin-releasing factor overexpression in mice abrogates sex differences in body weight, visceral fat, and food intake response to a fast and alters levels of feeding regulatory hormones.

Lixin Wang, Miriam Goebel-Stengel, Pu-Qing Yuan, Andreas Stengel, Yvette Taché

Open access · goldAbstract read
In one paragraph

Article in Biology of sex differences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Lixin WangCURE/Digestive Diseases Research Center and Center for Neurobiology of Stress, Department of Medicine, Digestive Diseases Division, David Geffen School of Medicine, University of California at Los Angeles and Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, California USA.ORCID 0000-0001-8140-6325
Miriam Goebel-StengelCURE/Digestive Diseases Research Center and Center for Neurobiology of Stress, Department of Medicine, Digestive Diseases Division, David Geffen School of Medicine, University of California at Los Angeles and Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, California USA ; Present address: Department for Internal Medicine, Martin-Luther-Krankenhaus, Caspar-Theyß-Str. 27-31, 14193 Berlin, Germany.
Pu-Qing YuanCURE/Digestive Diseases Research Center and Center for Neurobiology of Stress, Department of Medicine, Digestive Diseases Division, David Geffen School of Medicine, University of California at Los Angeles and Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, California USA.
Andreas StengelCURE/Digestive Diseases Research Center and Center for Neurobiology of Stress, Department of Medicine, Digestive Diseases Division, David Geffen School of Medicine, University of California at Los Angeles and Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, California USA ; Present address: Department for Psychosomatic Medicine, Charité Berlin, Hindenburgdamm 30, 12203 Berlin, Germany.
Yvette TachéCURE/Digestive Diseases Research Center and Center for Neurobiology of Stress, Department of Medicine, Digestive Diseases Division, David Geffen School of Medicine, University of California at Los Angeles and Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, California USA.
University of California, Los Angeles · US

Funding

Pilot and Feasibility ProgramP30DK041301 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1990 to 2019
$18.0M
Women's Health and Functional Visceral Disorders CenterP50DK064539 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MAYER, EMERAN A · 2002 to 2017
$17.5M
Ghrelin Agonists Multiple Beneficial Effects on Parkinson's Non-Motor SymptomsI01RX001685 · VA · VA GREATER LOS ANGELES HEALTHCARE SYSTEM · PI WANG, LIXIN · 2015 to 2020
–
NIDDK NIH HHS P30 DK041301NIDDK NIH HHS P50 DK064539RRD VA I01 RX001685
6 · The paper itself

Abstract

backgroundCorticotropin-releasing factor overexpressing (CRF-OE) male mice showed an inhibited feeding response to a fast, and lower plasma acyl ghrelin and Fos expression in the arcuate nucleus compared to wild-type (WT) mice. We investigated whether hormones and hypothalamic feeding signals are impaired in CRF-OE mice and the influence of sex.

methodsMale and female CRF-OE mice and WT littermates (4-6 months old) fed

resultsUnder fed conditions, compared to WT, CRF-OE mice have increased adrenal glands and perigonadal fat weight, plasma corticosterone, leptin and insulin, and hypothalamic leptin receptor and decreased plasma acyl ghrelin. Compared to male, female WT mice have lower body and perigonadal fat and plasma leptin but higher adrenal glands weights. CRF-OE mice lost these sex differences except for the adrenals. Male CRF-OE and WT mice did not differ in hypothalamic expression of neuropeptide Y (NPY) and proopiomelanocortin (POMC), while female CRF-OE compared to female WT and male CRF-OE had higher NPY mRNA levels. After fasting, female WT mice lost more body weight and ate more food than male WT, while CRF-OE mice had reduced body weight loss and inhibited food intake without sex difference. In male WT mice, fasting reduced plasma insulin and leptin and increased acyl ghrelin and corticosterone while female WT showed only a rise in corticosterone. In CRF-OE mice, fasting reduced insulin while leptin, acyl ghrelin and corticosterone were unchanged with no sex difference. Fasting blood glucose was higher in CRF-OE with female > male. In WT mice, fasting increased hypothalamic NPY expression in both sexes and decreased POMC only in males, while in CRF-OE mice, NPY did not change, and POMC decreased in males and increased in females.

conclusionsThese data indicate that CRF-OE mice have abnormal basal and fasting circulating hormones and hypothalamic feeding-related signals. CRF-OE also abolishes the sex difference in body weight, abdominal fat, and fasting-induced feeding and changes in plasma levels of leptin and acyl ghrelin.

Indexed as

Sex CharacteristicsAnimalsBlood GlucoseBody WeightCorticosteroneCorticotropin-Releasing HormoneEatingFastingFemaleHypothalamusIntra-Abdominal FatMaleMice, TransgenicNeuropeptide YPeptide HormonesReceptors, Corticotropin-Releasing HormoneBlood GlucoseCorticosteroneCorticotropin-Releasing HormoneCRF receptor type 2leptin receptor, mouseNeuropeptide YPeptide HormonesReceptors, Corticotropin-Releasing HormoneReceptors, LeptinAdrenalsCorticosteroneCRF-overexpressing miceFastingGhrelinGlucoseHypothalamic neuropeptide YInsulinLeptinSex differenceVisceral fat

Identifiers

PMID28101317
PMCPMC5237138
OpenAlexW2572222530

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.