Evidence map›Paper›PMID 20215417›Full record

ArticlePhysiological genomics2010

High-fat diet leads to tissue-specific changes reflecting risk factors for diseases in DBA/2J mice.

Rachael S Hageman, Asja Wagener, Claudia Hantschel, Karen L Svenson, Gary A Churchill, Gudrun A Brockmann

Abstract read
In one paragraph

Article in Physiological genomics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
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  10. Review
  11. Knockout of the X-linkedFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
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  13. Reg3 Proteins as Gut Hormones?Endocrinology · 2019
    Review
  14. Article
  15. APMAP interacts with lysyl oxidase-like proteins, and disruption ofFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
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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

6 authors at 2 institutions in 2 countries.

Rachael S HagemanThe Jackson Laboratory, Bar Harbor, Maine, USA.
Asja Wagener
Claudia Hantschel
Karen L Svenson
Gary A Churchill
Gudrun A Brockmann
Humboldt-Universität zu Berlin · DEJackson Laboratory · US

Funding

UNC and PERLEGEN, IncP50GM076468 · NIGMS · JACKSON LABORATORY · PI CHURCHILL, GARY A · 2006 to 2015
$31.0M
Bayesian Dynamic Genome Scale Modeling of HDL Cholesterol TransportF32HL095240 · NHLBI · JACKSON LABORATORY · PI HAGEMAN, RACHAEL · 2009 to 2011
$135k
NHLBI NIH HHS 1F32-HL-095240-01NIGMS NIH HHS GM-076468
6 · The paper itself

Abstract

The aim of this study was to characterize the responses of individual tissues to high-fat feeding as a function of mass, fat composition, and transcript abundance. We examined a panel of eight tissues [5 white adipose tissues (WAT), brown adipose tissue (BAT), liver, muscle] obtained from DBA/2J mice on either a standard breeding diet (SBD) or a high-fat diet (HFD). HFD led to weight gain, decreased insulin sensitivity, and tissue-specific responses, including inflammation, in these mice. The dietary fatty acids were partially metabolized and converted in both liver and fat tissues. Saturated fatty acids (SFA) were converted in the liver to monounsaturated fatty acids (MUFA) and polyunsaturated fatty acids (PUFA), and oleic acid (C18:1) was the preferred MUFA for storage of excess energy in all tissues of HFD-fed mice. Transcriptional changes largely reflected the tissue-specific fat deposition. SFA were negatively correlated with genes in the collagen family and processes involving the extracellular matrix. We propose a novel role of the tryptophan hydroxylase 2 (Tph2) gene in adipose tissues of diet-induced obesity. Tissue-specific responses to HFD were identified. Liver steatosis was evident in HFD-fed mice. Gonadal, retroperitoneal and subcutaneous adipose tissue and BAT exhibited severe inflammatory and immune responses. Mesenteric adipose tissue was the most metabolically active adipose tissue. Gluteal adipose tissue had the highest mass gain but was sluggish in its metabolism. In HFD conditions, BAT functioned largely like WAT in its role as a depot for excess energy, whereas WAT played a role in thermogenesis.

Indexed as

Adipose TissueAdipose Tissue, BrownAnimalsDietary FatsFatsFatty AcidsFatty Acids, UnsaturatedFatty LiverGene Expression ProfilingGlucose Tolerance TestLiverMaleMiceMice, Inbred DBAPrincipal Component AnalysisTryptophan HydroxylaseDietary FatsFatsFatty AcidsFatty Acids, UnsaturatedTph2 protein, mouseTryptophan Hydroxylase

Identifiers

PMID20215417
PMCPMC2888560
OpenAlexW2112886301

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.