Evidence map›Paper›PMID 26115368›Full record

ArticleGrowth factors (Chur, Switzerland)2015

Beta-adrenergic receptor agonist decreases VEGF levels through altered eNOS and PKC signaling in diabetic retina.

Youde Jiang, Qiuhua Zhang, Jena J Steinle

Open access · greenAbstract read
In one paragraph

Article in Growth factors (Chur, Switzerland), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Review
  3. The βAdvances in pharmacological and pharmaceutical sciences · 2024
    Review
  4. Article
  5. Review
  6. Cellular targets in diabetic retinopathy therapy.World journal of diabetes · 2021
    Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Aloe-emodin suppresses hypoxia-induced retinal angiogenesisInternational journal of biological sciences · 2016
    Article
  13. Article
  14. Article
  15. Effect of miR-200b on retinal endothelial cell function under high glucose environment.International journal of clinical and experimental pathology · 2015
    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

3 authors at 2 institutions in 1 country.

Youde Jianga Department of Anatomy and Cell Biology , Wayne State University , Detroit , MI , USA .
Qiuhua Zhangb Department of Ophthalmology , University of Tennessee Health Science Center , Memphis , TN , USA , and.
Jena J Steinlea Department of Anatomy and Cell Biology , Wayne State University , Detroit , MI , USA .
Wayne State University · USUniversity of Tennessee Health Science Center · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
VISION RESEARCH--COREP30EY004068 · NEI · WAYNE STATE UNIVERSITY · PI LINDA D HAZLETT · 1985 to 2026
$13.2M
Compound 49b Prevents Retinal Endothelial Cell Death Through IGFBP-3 LevelsR01EY022045 · NEI · WAYNE STATE UNIVERSITY · PI STEINLE, JENA J · 2012 to 2016
$1.8M
NEI NIH HHS P30 EY004068NEI NIH HHS P30EY04068NEI NIH HHS R01 EY022045NEI NIH HHS R01EY022045NIDDK NIH HHS P30 DK020572
6 · The paper itself

Abstract

Vascular endothelial cell growth factor (VEGF) is increased in diabetic macular edema. Compound 49b, a novel β-adrenergic receptor agonist, is protective in a type 1 diabetic rat model. We questioned whether Compound 49b could decrease VEGF levels, suggesting that Compound 49b may be effective against edema. Two-month diabetic rats received topical Compound 49b for 7 days only and/or insulin-like growth factor binding protein 3 (IGFBP-3) siRNA. We also measured endothelial nitric oxide synthase (eNOS) and protein kinase C (PKC)ζ and PKCδ phosphorylation. Retinal endothelial cells (RECs) cultured in high glucose were treated with Compound 49b and IGFBP-3 siRNA for evaluation of the same signaling pathways. Compound 49b significantly decreased VEGF through increased IGFBP-3 in the diabetic retina. Compound 49b also reduced eNOS, PKCζ and PKCδ phosphorylation in the diabetic retina and REC. Compound 49b regulated a number of proteins involved in REC barrier properties.

Indexed as

Adrenergic beta-AgonistsAnimalsCells, CulturedDiabetes Mellitus, ExperimentalDiabetic RetinopathyEndothelial CellsInsulin-Like Growth Factor Binding Protein 3IsoenzymesMacular EdemaMaleNitric Oxide Synthase Type IIINorepinephrinePhenethylaminesProtein Kinase CProtein Kinase C-deltaProtein Kinase C-thetaAdrenergic beta-AgonistsInsulin-Like Growth Factor Binding Protein 3IsoenzymesNitric Oxide Synthase Type IIINorepinephrineNos3 protein, ratPhenethylaminesPrkcq protein, ratProtein Kinase CProtein Kinase C-deltaProtein Kinase C-thetaProtein Kinase C zetaRNA, Small InterferingStreptozocinVascular Endothelial Growth Factor Avascular endothelial growth factor A, ratBeta-adrenergic receptordiabetic retinopathyVEGF

Identifiers

PMID26115368
PMCPMC4791949
OpenAlexW2313489940

What OpenQuestion holds

Textmetadata
LicenceTDM
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.