Evidence map›Paper›PMID 27923977›Full record

ArticlePhysiological reports2016

Absence of renal enlargement in fructose-fed proximal-tubule-select insulin receptor (IR), insulin-like-growth factor receptor (IGF1R) double knockout mice.

Lijun Li, Marcus Byrd, Kwame Doh, Patrice D Dixon, Hwal Lee, Swasti Tiwari, Carolyn M Ecelbarger

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Acid Loading Unmasks Glucose Homeostatic Instability in Proximal-Tubule-Targeted Insulin/Insulin-Like-Growth-Factor-1 Receptor Dual Knockout Mice.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2020
    Article
  6. 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

7 authors at 1 institution in 2 countries.

Lijun LiDepartment of Medicine, Georgetown University, Washington, District of Columbia.
Marcus ByrdDepartment of Medicine, Georgetown University, Washington, District of Columbia.
Kwame DohDepartment of Medicine, Georgetown University, Washington, District of Columbia.
Patrice D DixonDepartment of Medicine, Georgetown University, Washington, District of Columbia.
Hwal LeeDepartment of Medicine, Georgetown University, Washington, District of Columbia.
Swasti TiwariDepartment of Medicine, Georgetown University, Washington, District of Columbia.
Carolyn M EcelbargerDepartment of Medicine, Georgetown University, Washington, District of Columbia ecelbarc@georgetown.edu.
Georgetown University · US

Funding

Role of Insulin Receptors in the KidneyR01DK082507 · NIDDK · GEORGETOWN UNIVERSITY · PI ECELBARGER, CAROLYN MARY · 2010 to 2013
$1.3M
NIDDK NIH HHS R01 DK082507
6 · The paper itself

Abstract

The major site of fructose metabolism in the kidney is the proximal tubule (PT). To test whether insulin and/or IGF1 signaling in the PT is involved in renal structural/functional responses to dietary fructose, we bred mice with dual knockout (KO) of the insulin receptor (IR) and the IGF1 receptor (IGF1R) in PT by Cre-lox recombination, using a γ-glutamyl transferase promoter. KO mice had slightly (~10%) reduced body and kidney weights, as well as, a reduction in mean protein-to-DNA ratio in kidney cortex suggesting smaller cell size. Under control diet, IR and IGF1R protein band densities were 30-50% (P < 0.05) lower than WT, and the relative difference was greater in male animals. Male, but not female KO, also had significantly reduced band densities for Akt (protein kinase B), phosphorylated Akt

Indexed as

AnimalsDietFemaleFructoseKidney Tubules, ProximalMaleMiceMice, Inbred C57BLOrgan SizeReceptor, IGF Type 1Receptor, InsulinSex FactorsSodium-Bicarbonate SymportersSodium-Hydrogen ExchangersSodium-Phosphate Cotransporter ProteinsTransforming Growth Factor betaFructoseReceptor, IGF Type 1Receptor, InsulinSodium-Bicarbonate SymportersSodium-Hydrogen ExchangersSodium-Phosphate Cotransporter ProteinsTransforming Growth Factor betaInsulin resistancemetabolic syndromerenal enlargementrenal tubular acidosissex differences

Identifiers

PMID27923977
PMCPMC5357825
OpenAlexW2559944576

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.