Evidence map›Paper›PMID 30301967›Full record

ArticleInternational journal of obesity (2005)2019

Temporal immmunometabolic profiling of adipose tissue in HFD-induced obesity: manifestations of mast cells in fibrosis and senescence.

Durgesh Kumar, Sanket Kumar Pandya, Salil Varshney, Kripa Shankar, Sujith Rajan, Ankita Srivastava, Abhishek Gupta, Sanchita Gupta, Achchhe Lal Vishwakarma, Amit Misra and 1 more

Abstract read
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In one paragraph

Article in International journal of obesity (2005), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 13% 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, 27 citations in OpenAlex.

  1. Article
  2. Adipose tissue depot specific expression and regulation of fibrosis-related genes and proteins in experimental obesity.Mammalian genome : official journal of the International Mammalian Genome Society · 2024
    Article
  3. Prohibitions in the meta-inflammatory response: a review.Frontiers in molecular biosciences · 2024
    Review
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  14. Genetic Deletion ofNutrients · 2019
    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

11 authors at 2 institutions in 1 country.

Durgesh KumarDivision of Pharmacology, CSIR-Central Drug Research Institute, Lucknow, 226031, India.
Sanket Kumar PandyaAcademy of Scientific and Innovative Research, CSIR-Central Drug Research Institute, Lucknow, 226031, India.
Salil VarshneyDivision of Pharmacology, CSIR-Central Drug Research Institute, Lucknow, 226031, India.
Kripa ShankarDivision of Pharmacology, CSIR-Central Drug Research Institute, Lucknow, 226031, India.
Sujith RajanDivision of Pharmacology, CSIR-Central Drug Research Institute, Lucknow, 226031, India.
Ankita SrivastavaDivision of Pharmacology, CSIR-Central Drug Research Institute, Lucknow, 226031, India.
Abhishek GuptaDivision of Pharmacology, CSIR-Central Drug Research Institute, Lucknow, 226031, India.
Sanchita GuptaDivision of Pharmacology, CSIR-Central Drug Research Institute, Lucknow, 226031, India.
Achchhe Lal VishwakarmaSophisticated Analytical Instrument Facility, CSIR-Central Drug Research Institute, Lucknow, 226031, India.
Amit MisraDivision of Pharmaceutics and Pharmacokinetics, CSIR-Central Drug Research Institute, Lucknow, 226031, India.
Anil N GaikwadDivision of Pharmacology, CSIR-Central Drug Research Institute, Lucknow, 226031, India. anil_gaikwad@cdri.res.in.
Central Drug Research Institute · INAcademy of Scientific and Innovative Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesChronic low-grade inflammation/meta-inflammation in adipose tissue leads to obesity-associated metabolic complications. Despite growing understanding, the roles of immune cell subsets, their interrelationship, and chronological events leading to progression of obesity-associated insulin resistance (IR) remains unclear.

methodsWe carried out temporal immunometabolic profiling of adipose tissue from C57BL/6 mice fed a high-fat diet (HFD) for 4, 8, 12, 16, and 20 weeks. We used clodronate sodium liposomes (CLODs) to deplete macrophages and disodium cromoglycate sodium liposomes (DSCGs) to stabilize mast cells.

resultsIn the temporal HFD settings, mice showed progressive glucose intolerance, insulin resistance, and adipose tissue senescence. Histochemistry analysis of epididymal white adipose tissue (eWAT) using picro-sirius red and Masson's trichrome staining showed extensive collagen deposition in the 16th and 20th weeks. Flow cytometry analysis of the stromal vascular fraction (SVF) from eWAT revealed T-cell subsets as early-phase components and pro-inflammatory macrophages, as well as mast cells as the later phase components during obesity progression. In our therapeutic strategies, macrophage depletion by CLOD and mast stabilization by DSCG attenuated obesity, adipose tissue fibrosis, and improved whole-body glucose homeostasis. In addition, mast cell stabilization also attenuated senescence (p53 and X-gal staining) in eWAT, signifying the role of mast cells over macrophages during obesity.

conclusionNew-generation mast cell stabilizers can be exploited for the treatment of obesity-associated metabolic complications.

Indexed as

Diet, High-FatAdipose TissueAgingAnimalsDisease Models, AnimalFibrosisInflammationInsulin ResistanceMast CellsMiceMice, Inbred C57BLObesity

Identifiers

PMID30301967
OpenAlexW2896449230

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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.