Evidence map›Paper›PMID 24719784›Full record

ArticleAdipocyte2014

Short-term HFD does not alter lipolytic function of adipocytes.

Michael Sf Wiedemann, Stephan Wueest, Alexandra Grob, Flurin Item, Eugen J Schoenle, Daniel Konrad

Open access · goldAbstract read
In one paragraph

Article in Adipocyte, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 8 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

6 authors at 5 institutions in 5 countries.

Michael Sf WiedemannDivision of Pediatric Endocrinology and Diabetology; University Children's Hospital; Zurich, Switzerland ; Children's Research Center; University Children's Hospital; Zurich, Switzerland ; Zurich Center for Integrative Human Physiology; University of Zurich; Zurich, Switzerland.
Stephan WueestDivision of Pediatric Endocrinology and Diabetology; University Children's Hospital; Zurich, Switzerland ; Children's Research Center; University Children's Hospital; Zurich, Switzerland.
Alexandra GrobDivision of Pediatric Endocrinology and Diabetology; University Children's Hospital; Zurich, Switzerland ; Children's Research Center; University Children's Hospital; Zurich, Switzerland ; Institute of Human Movement Sciences; ETH Zurich; Zurich, Switzerland.
Flurin ItemDivision of Pediatric Endocrinology and Diabetology; University Children's Hospital; Zurich, Switzerland ; Children's Research Center; University Children's Hospital; Zurich, Switzerland.
Eugen J SchoenleDivision of Pediatric Endocrinology and Diabetology; University Children's Hospital; Zurich, Switzerland ; Children's Research Center; University Children's Hospital; Zurich, Switzerland.
Daniel KonradDivision of Pediatric Endocrinology and Diabetology; University Children's Hospital; Zurich, Switzerland ; Children's Research Center; University Children's Hospital; Zurich, Switzerland ; Zurich Center for Integrative Human Physiology; University of Zurich; Zurich, Switzerland.
Children's Clinical University Hospital · LVDiabetes Australia · AULaban/Bartenieff Institute of Movement Studies · USSwiss Integrative Center for Human Health · CHUniwersytecki Szpital Dziecięcy · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A short bout of high fat diet (HFD) impairs glucose tolerance and hepatic insulin sensitivity. We recently identified adipose tissue inflammation and resulting dysfunctional adipose tissue-liver cross-talk as an early event in the development of HFD-induced hepatic insulin resistance. In particular, reducing white adipose tissue (WAT) inflammation by adipocyte-specific depletion of Fas/CD95 protected mice from developing hepatic insulin resistance but not hepatic steatosis. Herein, we expanded our previous work and determined the impact of four days of HFD on lipolytic activity of isolated adipocytes. Compared with chow-fed mice, the degree of basal and isoproterenol-stimulated free fatty acid (FFA) and glycerol release was similar in HFD-fed animals. Moreover, insulin's ability to suppress lipolysis remained intact, suggesting retained insulin sensitivity. Despite unaltered lipolysis, circulating FFA concentrations were greatly increased in non-fasted HFD-fed mice. In conclusion, a short-term HFD challenge does not affect lipolytic function of adipocytes. The observed increase of circulating FFA levels in randomly fed animals may rather be the result of increased dietary fat supply.

Indexed as

adipose tissue–liver crosstalkdiabetes mellitusfat depotlipolysislipotoxicity

Identifiers

PMID24719784
PMCPMC3979875
OpenAlexW2018864477

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.