Evidence map›Paper›PMID 21071934›Full record

ArticleAmerican journal of nephrology2010

Chronic nitric oxide deficiency and progression of kidney disease after renal mass reduction in the C57Bl6 mouse.

Veronika Muller, You-Lin Tain, Byron Croker, Chris Baylis

Open access · bronzeAbstract read
In one paragraph

Article in American journal of nephrology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Vascular Function and Uric Acid-Lowering in Stage 3 CKD.Journal of the American Society of Nephrology : JASN · 2017
    Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. The NOS/NO System in Renal Programming and Reprogramming.Antioxidants (Basel, Switzerland) · 2023
    Review
  7. Article
  8. Reduced Renal Methylarginine Metabolism Protects against Progressive Kidney Damage.Journal of the American Society of Nephrology : JASN · 2015
    Article
  9. Article
  10. Assessment of vascular function in patients with chronic kidney disease.Journal of visualized experiments : JoVE · 2014
    Article
  11. Article
  12. Developmental programming of hypertension and kidney disease.International journal of nephrology · 2012
    Article
  13. Nitric oxide synthase derangements and hypertension in kidney disease.Current opinion in nephrology and hypertension · 2012
    Review
  14. 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

4 authors at 3 institutions in 3 countries.

Veronika MullerDepartment of Pulmonology, Semmelweis University, Budapest, Hungary.
You-Lin Tain
Byron Croker
Chris Baylis
Chang Gung University · TWNorth Florida/South Georgia Veterans Health System · USSemmelweis University · HU

Funding

Nitrix Oxide in Chronic Renal DiseaseR01DK056843 · NIDDK · WEST VIRGINIA UNIVERSITY · PI BAYLIS, CHRISTINE · 2001 to 2015
$3.4M
NIDDK NIH HHS R01 DK056843NIDDK NIH HHS R01 DK56843
6 · The paper itself

Abstract

BACKGROUND/

aimsthe C57Bl6 mouse is resistant to chronic kidney disease (CKD) induced by reduction of renal mass (RRM). Nitric oxide (NO) deficiency exacerbates CKD progression so this study investigated whether combination of RRM and NO deficiency would render the C57Bl6 mouse vulnerable to CKD.

methodswe used wild-type (WT) mice with RRM, chronic NO synthase (NOS) inhibition and a combination. Also, endothelial NOS (eNOS) knockout (KO) C57Bl6 mice were studied with and without RRM. Primary endpoints were albuminuria and structural damage.

resultsboth nonselective (+L-NAME) and neuronal NOS 'selective' (+7NI) NOS inhibition greatly exacerbated the albuminuria and structural damage seen with RRM in the WT mice; NOS inhibition alone had little effect. The eNOS KO mice showed marked structural damage and significant albuminuria in the shams and RRM produced minimal exacerbation of structural damage although the albuminuria was massively amplified.

conclusionthese studies demonstrate that the C57Bl6 mouse is rendered vulnerable to RRM-induced CKD when concomitant NO deficiency is produced. This observation supports previous work in CKD-resistant rats and suggests that NO deficiency is required for progression of CKD.

Indexed as

AlbuminuriaAnimalsDisease ProgressionEpithelial CellsKidneyKidney Failure, ChronicMaleMiceMice, Inbred C57BLMice, KnockoutNeuronsNitric OxideNitric Oxide SynthaseNitric OxideNitric Oxide Synthase

Identifiers

PMID21071934
PMCPMC2992651
OpenAlexW1968884508

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.