Evidence map›Paper›PMID 30118349›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2018

Inhibition of autotaxin alleviates inflammation and increases the expression of sodium-dependent glucose cotransporter 1 and Na

Peijian He, Abedul Haque, Songbai Lin, Fabio Cominelli, C Chris Yun

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

5 authors at 3 institutions in 1 country.

Peijian HeDivision of Digestive Diseases, Department of Medicine, Emory University School of Medicine , Atlanta, Georgia.
Abedul HaqueDivision of Digestive Diseases, Department of Medicine, Emory University School of Medicine , Atlanta, Georgia.
Songbai LinDivision of Digestive Diseases, Department of Medicine, Emory University School of Medicine , Atlanta, Georgia.
Fabio CominelliDepartment of Medicine, Case Digestive Health Research Institute, Case Western University School of Medicine , Cleveland, Ohio.
C Chris YunDivision of Digestive Diseases, Department of Medicine, Emory University School of Medicine , Atlanta, Georgia.
Veterans Health Administration · USEmory University · USWestern University of Health Sciences · US

Funding

The Cleveland Digestive Diseases Research Core Center (DDRCC)P30DK097948 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI Theresa Torres Pizarro · 2015 to 2026
$15.6M
MECHANISMS OF EXPERIMENTAL CROHNS DISEASER01DK055812 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI COMINELLI, FABIO · 1999 to 2019
$4.9M
The function of lysophosphatidic acid receptor LPA5R in intestinal inflammation and epithelial damageR01DK116799 · NIDDK · EMORY UNIVERSITY · PI YUN, CHANGHYON CHRIS · 2018 to 2022
$2.5M
Regulation of Human NHE3 by UbiquitinationR01DK107719 · NIDDK · EMORY UNIVERSITY · PI YUN, CHANGHYON CHRIS · 2016 to 2019
$1.4M
Regulation of intestinal homeostasis and epithelial barrier by LPAI01BX002540 · VA · VETERANS HEALTH ADMINISTRATION · PI YUN, CHANGHYON CHRIS · 2015 to 2018
–
BLRD VA I01 BX002540NIDDK NIH HHS P30 DK097948NIDDK NIH HHS R01 DK055812NIDDK NIH HHS R01 DK107719NIDDK NIH HHS R01 DK116799
6 · The paper itself

Abstract

Crohn's disease (CD) is a chronic, relapsing, inflammatory disease that is often associated with malnutrition because of inflammation in the small intestine. Autotaxin (ATX) is a secreted enzyme that produces extracellular lysophosphatidic acid. Increasing evidence suggests that ATX is upregulated during inflammation, and inhibition of ATX has been effective in attenuating chronic inflammatory conditions, such as arthritis and pulmonary fibrosis. This study aims to determine whether inhibition of ATX alleviates CD-associated inflammation and malnutrition by using SAMP1/Fc mice, a model of CD-like ileitis. SAMP1/Fc mice were treated the ATX inhibitor PF-8380 for 4 wk. Inhibition of ATX led to increased weight gain in SAMP1/Fc mice, decreased T helper 2 cytokine expression, including IL-4, IL-5, and IL-13, and attenuated immune cell migration. SAMP1/Fc mice have low expression of Na

Indexed as

AnimalsAnti-Inflammatory AgentsBenzoxazolesCaco-2 CellsCytokinesHumansIleitisIleumIntestinal AbsorptionLysophospholipase DMaleMembrane ProteinsMiceNuclear ProteinsPhosphoric Diester HydrolasesPiperazines6-(3-(piperazin-1-yl)propanoyl)benzo(d)oxazol-2(3H)-oneAnti-Inflammatory AgentsBenzoxazolesCytokinesLysophospholipase DMembrane ProteinsNuclear ProteinsPhosphoric Diester HydrolasesPiperazinesSamp1 protein, mouseSlc5a1 protein, mouseSodium-Glucose Transporter 1Sodium-Hydrogen Exchanger 3autotaxininflammatory bowel diseasesNa-dependent glucose transporter 1Na/H exchanger 3

Identifiers

PMID30118349
PMCPMC6293258
OpenAlexW2887918505

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.