Evidence map›Paper›PMID 20110732›Full record

ArticleNephron. Experimental nephrology2010

Kidneys of Alb/TGF-beta1 transgenic mice are deficient in retinoic acid and exogenous retinoic acid shows dose-dependent toxicity.

Qihe Xu, Bruce M Hendry, Malcolm Maden, Huiyan Lu, Yuen Fei Wong, Alexandra C Rankin, Mazhar Noor, Jeffrey B Kopp

Open access · greenAbstract read
In one paragraph

Article in Nephron. Experimental nephrology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Induction of retinol dehydrogenase 9 expression in podocytes attenuates kidney injury.Journal of the American Society of Nephrology : JASN · 2014
    Article
  4. Article
  5. Review
  6. Review
  7. 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 at 5 institutions in 2 countries.

Qihe XuDepartment of Renal Medicine, King's College London, London, UK. qihe.xu@kcl.ac.uk
Bruce M Hendry
Malcolm Maden
Huiyan Lu
Yuen Fei Wong
Alexandra C Rankin
Mazhar Noor
Jeffrey B Kopp
King's College London · GBKing's College School · GBNational Institute of Diabetes and Digestive and Kidney Diseases · USNational Institutes of Health · USUniversity of Florida · US

Funding

British Heart FoundationIntramural NIH HHS
6 · The paper itself

Abstract

backgroundAlb/TGF-beta(1) transgenic mice overexpress active transforming growth factor-beta(1) (TGF-beta(1)) in the liver, leading to increased circulating levels of the cytokine and progressive renal fibrosis. This study was designed to explore if exogenous all-trans retinoic acid (tRA) prevents renal fibrosis in this animal model.

methodsThe retinoid profile in kidney and liver of wild-type and Alb/TGF-beta(1) transgenic mice was examined by high-performance liquid chromatography and slow-release pellets containing different amounts of tRA were implanted subcutaneously to treat the Alb/TGF-beta(1) transgenic mice, starting at 1 week of age; mice were sacrificed 2 weeks later.

resultsKidneys of 3-week-old wild-type mice had abundant tRA, which was completely absent in kidneys of the transgenic mice. Low doses of tRA (6-10.7 mg/kg/day) failed to affect renal fibrosis although it tended to suppress the mRNA expression of some molecular markers of fibrosis and retinal dehydrogenase 2 (RALDH2), a gene encoding a key tRA-synthesising enzyme. These tendencies disappeared, mortality tended to increase and RALDH2 and connective tissue growth factor (CTGF) mRNAs significantly increased in the medium-dose group (12.7-18.8 mg/kg/day). High doses (20.1-27.4 mg/kg/day) showed even higher toxicity with increased renal fibrosis and significant mortality.

conclusionsAlb/TGF-beta(1) transgenic mice are characterised by depletion of endogenous renal tRA. Exogenous tRA dose-dependently increases mortality and kidney fibrosis, which is associated with dose-dependent regulation of renal RALDH2 and CTGF mRNA expression.

Indexed as

AnimalsConnective Tissue Growth FactorDisease Models, AnimalFibrosisKidneyLiverMaleMiceMice, Inbred C57BLMice, TransgenicTransforming Growth Factor beta1TretinoinCCN2 protein, mouseConnective Tissue Growth FactorTransforming Growth Factor beta1Tretinoin

Identifiers

PMID20110732
PMCPMC2865400
OpenAlexW2032635299

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.