Evidence map›Paper›PMID 30372743›Full record

ArticleInvestigative ophthalmology & visual science2018

Constriction of Retinal Venules to Endothelin-1: Obligatory Roles of ETA Receptors, Extracellular Calcium Entry, and Rho Kinase.

Yen-Lin Chen, Yi Ren, Wenjuan Xu, Robert H Rosa, Lih Kuo, Travis W Hein

Open access · goldAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Sitting leg vasculopathy: potential adaptations beyond the endothelium.American journal of physiology. Heart and circulatory physiology · 2024
    Review
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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

6 authors at 2 institutions in 1 country.

Yen-Lin ChenDepartment of Medical Physiology, College of Medicine, Texas A&M University Health Science Center, Temple, Texas, United States.
Yi RenDepartment of Medical Physiology, College of Medicine, Texas A&M University Health Science Center, Temple, Texas, United States.
Wenjuan XuDepartment of Medical Physiology, College of Medicine, Texas A&M University Health Science Center, Temple, Texas, United States.
Robert H RosaDepartment of Medical Physiology, College of Medicine, Texas A&M University Health Science Center, Temple, Texas, United States.
Lih KuoDepartment of Medical Physiology, College of Medicine, Texas A&M University Health Science Center, Temple, Texas, United States.
Travis W HeinDepartment of Medical Physiology, College of Medicine, Texas A&M University Health Science Center, Temple, Texas, United States.
Texas A&M University · USBaylor Scott & White Health · US

Funding

Roles of LOX-1 and Stress-Activated Kinases in Retinal Dysfunction during Early DiabetesR01EY024624 · NEI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI HEIN, TRAVIS W · 2015 to 2017
$1.4M
Vasomotor Dysfunction of Retinal Arterioles in DiabetesR01EY023335 · NEI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI HEIN, TRAVIS W · 2014 to 2016
$1.1M
NEI NIH HHS R01 EY023335NEI NIH HHS R01 EY024624
6 · The paper itself

Abstract

Purpose: Endothelin-1 (ET-1) is a potent vasoconstrictor peptide implicated in retinal venous pathologies such as diabetic retinopathy and retinal vein occlusion. However, underlying mechanisms contributing to venular constriction remain unknown. Thus, we examined the roles of ET-1 receptors, extracellular calcium (Ca2+), L-type voltage-operated calcium channels (L-VOCCs), Rho kinase (ROCK), and protein kinase C (PKC) in ET-1-induced constriction of retinal venules. Methods: Porcine retinal venules were isolated and pressurized for vasoreactivity study using videomicroscopic techniques. Protein and mRNA were analyzed using molecular tools. Results: Retinal venules developed basal tone and constricted concentration-dependently to ET-1. The ETA receptor (ETAR) antagonist BQ123 abolished venular constriction to ET-1, but ETB receptor (ETBR) antagonist BQ788 had no effect on vasoconstriction. The ETBR agonist sarafotoxin S6c did not elicit vasomotor activity. In the absence of extracellular Ca2+, venules lost basal tone and ET-1-induced constriction was nearly abolished. Although L-VOCC inhibitor nifedipine also reduced basal tone and blocked vasoconstriction to L-VOCC activator Bay K8644, constriction of venules to ET-1 remained. The ROCK inhibitor H-1152 but not PKC inhibitor Gö 6983 prevented ET-1-induced vasoconstriction. Protein and mRNA expressions of ETARs and ETBRs, along with ROCK1 and ROCK2 isoforms, were detected in retinal venules. Conclusions: Extracellular Ca2+ entry via L-VOCCs is essential for developing and maintaining basal tone of porcine retinal venules. ET-1 causes significant constriction of retinal venules by activating ETARs and extracellular Ca2+ entry independent of L-VOCCs. Activation of ROCK signaling, without involvement of PKC, appears to mediate venular constriction to ET-1 in the porcine retina.

Indexed as

AnimalsBlotting, WesternCalciumCalcium Channels, L-TypeEndothelin-1Endothelin B Receptor AntagonistsEndothelin Receptor AntagonistsFemaleMaleOligopeptidesPeptides, CyclicPiperidinesProtein Kinase CReal-Time Polymerase Chain ReactionReceptor, Endothelin ARetinal VeinBQ 788CalciumCalcium Channels, L-Typecyclo(Trp-Asp-Pro-Val-Leu)Endothelin-1Endothelin B Receptor AntagonistsEndothelin Receptor AntagonistsOligopeptidesPeptides, CyclicPiperidinesProtein Kinase CReceptor, Endothelin Arho-Associated KinasesRNA, Messenger

Identifiers

PMID30372743
PMCPMC6203175
OpenAlexW2898867347

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.