Evidence map›Paper›PMID 24595384›Full record

ArticleInvestigative ophthalmology & visual science2014

Pilocarpine-induced dilation of Schlemm's canal and prevention of lumen collapse at elevated intraocular pressures in living mice visualized by OCT.

Guorong Li, Sina Farsiu, Stephanie J Chiu, Pedro Gonzalez, Elke Lütjen-Drecoll, Darryl R Overby, W Daniel Stamer

Open access · bronzeAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
9.7field-weighted citation impact, top 1% 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

56 citing papers in PubMed, 95 citations in OpenAlex.

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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

7 authors at 3 institutions in 3 countries.

Guorong LiDepartment of Ophthalmology, Duke University, Durham, North Carolina, United States.
Sina FarsiuDepartment of Ophthalmology, Duke University, Durham, North Carolina, United States Department of Biomedical Engineering, Duke University, Durham, North Carolina, United States.
Stephanie J ChiuDepartment of Biomedical Engineering, Duke University, Durham, North Carolina, United States.
Pedro GonzalezDepartment of Ophthalmology, Duke University, Durham, North Carolina, United States.
Elke Lütjen-DrecollDepartment of Anatomie II, University Erlangen-Nürnberg, Germany.
Darryl R OverbyDepartment of Bioengineering, Imperial College London, London, United Kingdom.
W Daniel StamerDepartment of Ophthalmology, Duke University, Durham, North Carolina, United States Department of Biomedical Engineering, Duke University, Durham, North Carolina, United States.
Duke University · USFriedrich-Alexander-Universität Erlangen-Nürnberg · DEImperial College London · GB

Funding

VISION RESEARCHP30EY005722 · NEI · DUKE UNIVERSITY · PI Vadim Y Arshavsky · 1985 to 2026
$19.3M
eNOS-Dependent Mechanoregulation of Intraocular PressureR01EY022359 · NEI · DUKE UNIVERSITY · PI STAMER, W DANIEL · 2012 to 2025
$5.6M
Quantitative assessment of glaucomatous conventional outflow dynamicsR01EY030124 · NEI · DUKE UNIVERSITY · PI C ROSS ETHIER, Sina Farsiu · 2019 to 2026
$4.0M
NEI NIH HHS EY005722NEI NIH HHS EY022359NEI NIH HHS P30 EY005722NEI NIH HHS R01 EY022359NEI NIH HHS R01 EY030124
6 · The paper itself

Abstract

purposeThe goal was to assess effects of IOP and pilocarpine-induced ciliary muscle contraction on conventional outflow pathway tissues in living anesthetized mice.

methodsIntraocular pressure was controlled by intracameral cannulation of mouse eyes while imaging using spectral-domain optical coherence tomography (SD-OCT). Time-lapse sagittal SD-OCT sections through Schlemm's canal (SC) were acquired while changing IOP stepwise between 10 and 45 mm Hg. After topical application of 1% pilocarpine, the series of IOP steps and imaging were repeated. Effects of pilocarpine on IOP and outflow facility in living mice were verified by rebound tonometry and flow measurements at three different IOPs, respectively. In vivo OCT images were compared with eyes analyzed by standard histology.

resultsIn living mice imaged by SD-OCT, the lumen of SC progressively collapsed with increasing IOP, reaching near complete closure at 20 mm Hg. Schlemm's canal collapse was reversible, with the lumen opening within minutes after returning IOP from 45 to 10 mm Hg. Pilocarpine-induced ciliary muscle contraction changed SC lumen area by 131.6% ± 21.0% compared with untreated controls at 10 mm Hg, opened the trabecular meshwork, and prevented complete collapse of the SC lumen at higher pressures. Similar results were observed by standard histology. Pilocarpine increased outflow facility 4-fold (P = 0.02) and lowered IOP (16.46 ± 2.23 vs. 11.08 ± 2.28 mm Hg, P = 0.03).

conclusionsSpectral-domain OCT was effective at visualizing changes in SC lumen in living mice. Results with pilocarpine are consistent with the concept that a primary role for the ciliary muscle is to prevent collapse of SC.

Indexed as

AnimalsAqueous HumorCiliary BodyDisease Models, AnimalIntraocular PressureMiceMuscarinic AgonistsOcular HypertensionPilocarpineTomography, Optical CoherenceTrabecular MeshworkMuscarinic AgonistsPilocarpineaqueous humorglaucomaocular hypertensionoptical coherence tomographypilocarpinetrabecular meshwork

Identifiers

PMID24595384
PMCPMC4062397
OpenAlexW2011358704

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.