Evidence map›Paper›PMID 20435598›Full record

ArticleInvestigative ophthalmology & visual science2010

Cellular basis for bimatoprost effects on human conventional outflow.

W Daniel Stamer, David Piwnica, Thierry Jolas, Robert W Carling, Clive L Cornell, Hans Fliri, Jose Martos, Simon N Pettit, Jenny W Wang, David F Woodward

Open access · greenAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 41 citations in OpenAlex.

  1. From Eye Care to Hair Growth: Bimatoprost.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  2. Next generation therapeutics for retinal neurodegenerative diseases.Journal of controlled release : official journal of the Controlled Release Society · 2024
    Review
  3. Review
  4. Review
  5. Matrix Metalloproteinases and Glaucoma Treatment.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics · 2020
    Review
  6. Review
  7. Article
  8. Article
  9. Aqueous humor outflow: dynamics and disease.Investigative ophthalmology & visual science · 2015
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Effects of prostaglandin analogues on aqueous humor outflow pathways.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics
    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

10 authors at 2 institutions in 1 country.

W Daniel StamerDepartment of Ophthalmology and Vision Science, The University of Arizona, Tucson, Arizona 85711, USA. dstamer@eyes.arizona.edu
David Piwnica
Thierry Jolas
Robert W Carling
Clive L Cornell
Hans Fliri
Jose Martos
Simon N Pettit
Jenny W Wang
David F Woodward
Allergan (United States) · USUniversity of Arizona · US

Funding

MOLECULAR BASIS OF MYOCILIN FUNCTION IN THE HUMAN EYER01EY012797 · NEI · UNIVERSITY OF ARIZONA · PI STAMER, W DANIEL · 2001 to 2010
$2.2M
CADHERIN DYNAMICS AND GLAUCOMAR01EY017007 · NEI · UNIVERSITY OF ARIZONA · PI STAMER, W DANIEL · 2006 to 2010
$1.7M
NEI NIH HHS EY12797NEI NIH HHS EY17007NEI NIH HHS R01 EY012797NEI NIH HHS R01 EY017007
6 · The paper itself

Abstract

purposeBimatoprost is a widely used ocular hypotensive agent to treat glaucoma. It lowers intraocular pressure in humans by increasing both pressure-independent (uveoscleral) and pressure-dependent (conventional) aqueous humor outflow. The present study specifically examines bimatoprost effects on the cells that populate human outflow tissues.

methodsThe authors tested for prostamide receptor activation in primary cultures of human trabecular meshwork (TM), Schlemm's canal (SC), and ciliary smooth muscle (CSM) cells using cellular dielectric spectroscopy (CDS).

resultsThe authors observed that bimatoprost produced an immediate and concentration-dependent increase in cell monolayer impedance for TM, SC, and CSM cells with EC(50) values of 4.3, 1.2, and 1.7 nM, respectively; corresponding to decreased cell contractility. Notably, in TM, SC, and CSM cells, bimatoprost was approximately equipotent to the selective FP receptor agonists fluprostenol and 17-phenyl PGF(2α). Bimatoprost effects were insensitive to cholera toxin and pertussis toxin but were abolished by phorbol 12-myristate 13-acetate pretreatment, suggesting Gq-involvement in cell signaling. The effects of bimatoprost on TM and SC cells were inhibited by the prostamide receptor antagonist AGN211334, with IC(50) values of 1.2 and 3.3 μM, respectively. Interestingly, AGN211334 behaved as an apparent inverse agonist in CDS assays involving TM cells but as a neutral prostamide antagonist with SC cells.

conclusionsTaken together, results suggest that bimatoprost specifically activates receptors in both cell types of the human conventional outflow pathway to modify intraocular pressure. However, only TM cell monolayers appear to have autocrine, or agonist-independent, receptor signaling that is sensitive to a prostamide receptor antagonist.

Indexed as

ActinsAdultAgedAmidesAntihypertensive AgentsAqueous HumorBimatoprostCells, CulturedCiliary BodyCloprostenolCorneaDose-Response Relationship, DrugElectric ImpedanceHumansInfantIntraocular PressureActinsAmidesAntihypertensive AgentsBimatoprostCloprostenolprostaglandin F2alpha receptorReceptors, Prostaglandin

Identifiers

PMID20435598
PMCPMC3066606
OpenAlexW1995636548

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.