Evidence map›Paper›PMID 24915004›Full record

ArticlePloS one2014

Artemisia scoparia enhances adipocyte development and endocrine function in vitro and enhances insulin action in vivo.

Allison J Richard, Scott Fuller, Veaceslav Fedorcenco, Robbie Beyl, Thomas P Burris, Randall Mynatt, David M Ribnicky, Jacqueline M Stephens

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Prenylated Coumaric Acids fromJournal of natural products · 2021
    Article
  7. The Role of Resveratrol Administration in Human Obesity.International journal of molecular sciences · 2021
    Review
  8. Frontiers in endocrinology · 2021
    Review
  9. The potential role of sesquiterpene lactones isolated from medicinal plants in the treatment of the metabolic syndrome - A review.South African journal of botany : official journal of the South African Association of Botanists = Suid-Afrikaanse tydskrif vir plantkunde : amptelike tydskrif van die Suid-Afrikaanse Genootskap van Plantkundiges · 2020
    Review
  10. Article
  11. Article
  12. Chloroplast Genome Sequence ofPlants (Basel, Switzerland) · 2019
    Article
  13. Article
  14. Distinct Fractions of anFrontiers in nutrition · 2019
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

8 authors.

Allison J RichardPennington Biomedical Research Center, Louisiana State University, Baton Rouge, Louisiana, United States of America.
Scott FullerPennington Biomedical Research Center, Louisiana State University, Baton Rouge, Louisiana, United States of America.
Veaceslav FedorcencoPennington Biomedical Research Center, Louisiana State University, Baton Rouge, Louisiana, United States of America.
Robbie BeylPennington Biomedical Research Center, Louisiana State University, Baton Rouge, Louisiana, United States of America.
Thomas P BurrisDepartment of Pharmacological & Physiological Science, Saint Louis University, St. Louis, Missouri, United States of America.
Randall MynattPennington Biomedical Research Center, Louisiana State University, Baton Rouge, Louisiana, United States of America.
David M RibnickyDepartment of Plant Biology and Pathology, Rutgers University, New Brunswick, New Jersey, United States of America.
Jacqueline M StephensPennington Biomedical Research Center, Louisiana State University, Baton Rouge, Louisiana, United States of America.

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2012 to 2026
$69.1M
Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Leanne Maree Redman · 2005 to 2026
$26.5M
Pregnane and Glycosides and Obesity/llya RaskinP50AT002776 · NCCIH · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI RIBNICKY, DAVID M · 2005 to 2019
$24.9M
Mentoring Obesity and Diabetes Research in LouisianaP20GM103528 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2012 to 2015
$8.8M
Training in Botanical Approaches to Combat Metabolic SyndromeT32AT004094 · NCCIH · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI BRANTLEY, PHILLIP J, STEPHENS, JACQUELINE M · 2009 to 2024
$5.7M
NCCIH NIH HHS 2P50AT002776-06NCCIH NIH HHS P50 AT002776NCCIH NIH HHS T32 AT004094NIDDK NIH HHS 2P30DK072476NIDDK NIH HHS P30 DK072476NIGMS NIH HHS 1 U54 GM104940NIGMS NIH HHS 8 P20 GM103528NIGMS NIH HHS P20 GM103528NIGMS NIH HHS U54 GM104940
6 · The paper itself

Abstract

backgroundFailure of adipocytes to expand during periods of energy excess can result in undesirable metabolic consequences such as ectopic fat accumulation and insulin resistance. Blinded screening studies have indicated that Artemisia scoparia (SCO) extracts can enhance adipocyte differentiation and lipid accumulation in cultured adipocytes. The present study tested the hypothesis that SCO treatment modulates fat cell development and function in vitro and insulin sensitivity in adipose tissue in vivo.

methodsIn vitro experiments utilized a Gal4-PPARγ ligand binding domain (LBD) fusion protein-luciferase reporter assay to examine PPARγ activation. To investigate the ability of SCO to modulate adipogenesis and mature fat cell function in 3T3-L1 cells, neutral lipid accumulation, gene expression, and protein secretion were measured by Oil Red O staining, qRT-PCR, and immunoblotting, respectively. For the in vivo experiments, diet-induced obese (DIO) C57BL/6J mice were fed a high-fat diet (HFD) or HFD containing 1% w/w SCO for four weeks. Body weight and composition, food intake, and fasting glucose and insulin levels were measured. Phospho-activation and expression of insulin-sensitizing proteins in epididymal adipose tissue (eWAT) were measured by immunoblotting.

resultsEthanolic extracts of A. scoparia significantly activated the PPARγ LBD and enhanced lipid accumulation in differentiating 3T3-L1 cells. SCO increased the transcription of several PPARγ target genes in differentiating 3T3-L1 cells and rescued the negative effects of tumor necrosis factor α on production and secretion of adiponectin and monocyte chemoattractant protein-1 in fully differentiated fat cells. DIO mice treated with SCO had elevated adiponectin levels and increased phosphorylation of AMPKα in eWAT when compared to control mice. In SCO-treated mice, these changes were also associated with decreased fasting insulin and glucose levels.

conclusionSCO has metabolically beneficial effects on adipocytes in vitro and adipose tissue in vivo, highlighting its potential as a metabolically favorable botanical supplement.

Indexed as

3T3-L1 CellsAdipocytesAdipogenesisAdipokinesAdiponectinAdipose TissueAMP-Activated Protein KinasesAnimalsArtemisiaBlood GlucoseBody CompositionCell LineDose-Response Relationship, DrugEndocrine SystemGene Expression RegulationHumansAdipokinesAdiponectinAMP-Activated Protein KinasesBlood GlucoseInsulinPlant ExtractsPPAR gammaTumor Necrosis Factor-alpha

Identifiers

PMID24915004
PMCPMC4051605

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.