Evidence map›Paper›PMID 30979678›Full record

ArticleMolecular metabolism2019

Profound weight loss induces reactive astrogliosis in the arcuate nucleus of obese mice.

Luke Harrison, Katrin Pfuhlmann, Sonja C Schriever, Paul T Pfluger

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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  9. Hypothalamic inflammation in metabolic disorders and aging.Cellular and molecular life sciences : CMLS · 2021
    Review
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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

4 authors at 3 institutions in 1 country.

Luke HarrisonResearch Unit Neurobiology of Diabetes, Helmholtz Zentrum München, 85764, Neuherberg, Germany; Institute for Diabetes and Obesity, Helmholtz Zentrum München, 85764, Neuherberg, Germany; German Center for Diabetes Research (DZD), 85764, Neuherberg, Germany; Division of Metabolic Diseases, Technische Universität München, 80333, Munich, Germany.
Katrin PfuhlmannResearch Unit Neurobiology of Diabetes, Helmholtz Zentrum München, 85764, Neuherberg, Germany; Institute for Diabetes and Obesity, Helmholtz Zentrum München, 85764, Neuherberg, Germany; German Center for Diabetes Research (DZD), 85764, Neuherberg, Germany; Division of Metabolic Diseases, Technische Universität München, 80333, Munich, Germany.
Sonja C SchrieverResearch Unit Neurobiology of Diabetes, Helmholtz Zentrum München, 85764, Neuherberg, Germany; Institute for Diabetes and Obesity, Helmholtz Zentrum München, 85764, Neuherberg, Germany; German Center for Diabetes Research (DZD), 85764, Neuherberg, Germany.
Paul T PflugerResearch Unit Neurobiology of Diabetes, Helmholtz Zentrum München, 85764, Neuherberg, Germany; Institute for Diabetes and Obesity, Helmholtz Zentrum München, 85764, Neuherberg, Germany; German Center for Diabetes Research (DZD), 85764, Neuherberg, Germany. Electronic address: paul.pfluger@helmholtz-muenchen.de.
Helmholtz Zentrum München · DEDeutsches Diabetes-Zentrum e.V. · DEGerman Center for Diabetes Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveObesity has been linked to an inflammation like state in the hypothalamus, mainly characterized by reactive gliosis (RG) of astrocytes and microglia. Here, using two diet models or pharmacological treatment, we assessed the effects of mild and drastic weight loss on RG, in the context of high-fat diet (HFD) induced obesity.

methodsWe subjected HFD-induced obese (DIO) male C57BL/6J mice to a weight loss intervention with a switch to standard chow, calorie restriction (CR), or treatment with the Glp1 receptor agonist Exendin-4 (EX4). The severity of RG was estimated by an ordinal scoring system based on fluorescence intensities of glial fibrillary acidic protein, ionized calcium-binding adapter molecule 1 positive (Iba1), cell numbers, and morphological characteristics.

resultsIn contrast to previous reports, DIO mice fed chronically with HFD showed no differences in microglial or astrocytic RG, compared to chow controls. Moreover, mild or profound weight loss had no impact on microglial RG. However, astrocyte RG was increased in CR and EX4 groups compared to chow fed animals and strongly correlated to body weight loss. Profound weight loss by either CR or EX4 was further linked to increased levels of circulating non-esterified free fatty acids.

conclusionsOverall, our data demonstrate that in a chronically obese state, astrocyte and microglial RG is indifferent from that observed in age-matched chow controls. Nonetheless, profound acute weight loss can induce astrocyte RG in the hypothalamic arcuate nucleus, possibly due to increased circulating NEFAs. This suggests that astrocytes may sense acute changes to both the dietary environment and body weight.

Indexed as

Weight LossAnimalsAnti-Obesity AgentsArcuate Nucleus of HypothalamusAstrocytesCalcium-Binding ProteinsCaloric RestrictionExenatideGlial Fibrillary Acidic ProteinGliosisMaleMiceMice, Inbred C57BLMicrofilament ProteinsObesityAif1 protein, mouseAnti-Obesity AgentsCalcium-Binding ProteinsExenatideGlial Fibrillary Acidic ProteinMicrofilament ProteinsAstrocyteHypothalamusInflammationObesityReactive gliosisWeight loss

Identifiers

PMID30979678
PMCPMC6977167
OpenAlexW2929129696

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.