Evidence map›Paper›PMID 21209008›Full record

ArticleAmerican journal of physiology. Renal physiology2011

Vitamin D receptor agonist doxercalciferol modulates dietary fat-induced renal disease and renal lipid metabolism.

Xiaoxin X Wang, Tao Jiang, Yan Shen, Hannah Santamaria, Nathaniel Solis, Cynthia Arbeeny, Moshe Levi

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 2 pooled it
5.7field-weighted citation impact, top 4% 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

39 citing papers in PubMed, 2 syntheses or guidelines pooled it, 87 citations in OpenAlex.

  1. Pooled it
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  14. Use of 25-hydroxyvitamin DAnimal nutrition (Zhongguo xu mu shou yi xue hui) · 2021
    Review
  15. Review
  16. Review
  17. Review
  18. Vitamin D and Glomerulonephritis.Medicina (Kaunas, Lithuania) · 2021
    Review
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  20. 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

7 authors at 1 institution in 1 country.

Xiaoxin X WangDepartment of Medicine, University of Colorado, Denver, Colorado, USA.
Tao Jiang
Yan Shen
Hannah Santamaria
Nathaniel Solis
Cynthia Arbeeny
Moshe Levi
University of Colorado Denver · US

Funding

Role of FXR in Renal Disease of Metabolic Syndrome and AgingR01AG026529 · NIA · UNIVERSITY OF COLORADO DENVER · PI LEVI, MOSHE · 2007 to 2011
$1.8M
Novel Models of Diabetic NephropathyU01DK076134 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI LEVI, MOSHE · 2006 to 2010
$1.7M
NIA NIH HHS 3R01-AG-026529-03S1NIA NIH HHS R01 AG026529NIA NIH HHS R01-AG-026529NIDDK NIH HHS U01 DK076134NIDDK NIH HHS U01-DK-076134
6 · The paper itself

Abstract

Diet-induced obesity (DIO) and insulin resistance in mice are associated with proteinuria, renal mesangial expansion, accumulation of extracellular matrix proteins, and activation of oxidative stress, proinflammatory cytokines, profibrotic growth factors, and the sterol regulatory element binding proteins, SREBP-1 and SREBP-2, that mediate increases in fatty acid and cholesterol synthesis. The purpose of the present study was to determine whether treatment of DIO mice with the vitamin D receptor (VDR) agonist doxercalciferol (1α-hydroxyvitamin D2) prevents renal disease. Our results indicate that treatment of DIO mice with the VDR agonist decreases proteinuria, podocyte injury, mesangial expansion, and extracellular matrix protein accumulation. The VDR agonist also decreases macrophage infiltration, oxidative stress, proinflammatory cytokines, and profibrotic growth factors. Furthermore, the VDR agonist also prevents the activation of the renin-angiotensin-aldosterone system including the angiotensin II type 1 receptor and the mineralocorticoid receptor. An additional novel finding of our study is that activation of VDR results in decreased accumulation of neutral lipids (triglycerides and cholesterol) and expression of adipophilin in the kidney by decreasing SREBP-1 and SREBP-2 expression and target enzymes that mediate fatty acid and cholesterol synthesis and increasing expression of the farnesoid X receptor. This study therefore demonstrates multiple novel effects of VDR activation in the kidney which prevent renal manifestations of DIO in the kidney.

Indexed as

AnimalsCytokinesDietary FatsDisease Models, AnimalErgocalciferolsExtracellular Matrix ProteinsKidneyKidney DiseasesLipid MetabolismMacrophagesMaleMiceNF-kappa BObesityPodocytesProteinuria1 alpha-hydroxyergocalciferolCytokinesDietary FatsErgocalciferolsExtracellular Matrix ProteinsNF-kappa BReceptors, CalcitriolSterol Regulatory Element Binding Proteins

Identifiers

PMID21209008
PMCPMC3064139
OpenAlexW1998298665

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.