Evidence map›Paper›PMID 35018810›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2022

Fibroblast growth factor-21 improves insulin action in nonlactating ewes.

Cassandra L Lamb, Sarah L Giesy, Molly M McGuckin, James W Perfield, Anthony Butterfield, Mohammed Moniruzzaman, Norman J Haughey, Joseph W McFadden, Yves R Boisclair

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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

9 authors at 3 institutions in 1 country.

Cassandra L LambDepartment of Animal Science, Cornell University, Ithaca, New York.
Sarah L GiesyDepartment of Animal Science, Cornell University, Ithaca, New York.ORCID 0000-0002-0297-4883
Molly M McGuckinDepartment of Animal Science, Cornell University, Ithaca, New York.ORCID 0000-0002-2181-9213
James W PerfieldLilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana.
Anthony ButterfieldLilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana.
Mohammed MoniruzzamanDepartment of Neurology, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Norman J HaugheyDepartment of Neurology, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Joseph W McFaddenDepartment of Animal Science, Cornell University, Ithaca, New York.
Yves R BoisclairDepartment of Animal Science, Cornell University, Ithaca, New York.ORCID 0000-0002-6621-498X
Cornell University · USEli Lilly (United States) · USJohns Hopkins University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During metabolically demanding physiological states, ruminants and other mammals coordinate nutrient use among tissues by varying the set point of insulin action. This set point is regulated in part by metabolic hormones with some antagonizing (e.g., growth hormone and TNFα) and others potentiating (e.g., adiponectin) insulin action. Fibroblast growth factor-21 (FGF21) was recently identified as a sensitizing hormone in rodent and primate models of defective insulin action. FGF21 administration, however, failed to improve insulin action in dairy cows during the naturally occurring insulin resistance of lactation, raising the possibility that ruminants as a class of animals or lactation as a physiological state are unresponsive to FGF21. To start addressing this question, we asked whether FGF21 could improve insulin action in nonlactating ewes. Gene expression studies showed that the ovine FGF21 system resembles that of other species, with liver as the major site of FGF21 expression and adipose tissue as a target tissue based on high expression of the FGF21 receptor complex and activation of p44/42 extracellular signal-regulated kinase (ERK1/2) following exogenous FGF21 administration. FGF21 treatment for 13 days reduced plasma glucose and insulin over the entire treatment period and improved glucose disposal during a glucose tolerance test. FGF21 increased plasma adiponectin by

Indexed as

Insulin ResistanceAdiponectinAdipose TissueAnimalsBiomarkersBlood GlucoseFibroblast Growth FactorsInjections, IntravenousInjections, SubcutaneousInsulinKlotho ProteinsLiverSheep, DomesticTime FactorsAdiponectinBiomarkersBlood GlucoseFGF21 protein, humanFibroblast Growth FactorsInsulinKlotho Proteinsadiponectinadipose tissueceramideinsulin responsivenessruminant

Identifiers

PMID35018810
PMCPMC8816633
OpenAlexW4205108837

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.