Evidence map›Paper›PMID 39805385›Full record

ArticleExperimental eye research2025

A system for producing controlled elevation of intraocular pressure in awake Brown Norway rats.

John C Morrison, William Cepurna, Eliesa Ing, Elaine Johnson, Aryana Abtin, Susan Wentzien, Elizabeth White, Diana C Lozano

Abstract read
In one paragraph

Article in Experimental eye research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Neuroinflammation in glaucoma: a myriad of cellular pathways and players.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    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

8 authors.

John C MorrisonCasey Eye Institute, Oregon Health & Science University, United States. Electronic address: morrisoj@ohsu.edu.
William CepurnaCasey Eye Institute, Oregon Health & Science University, United States.
Eliesa IngCasey Eye Institute, Oregon Health & Science University, United States.
Elaine JohnsonCasey Eye Institute, Oregon Health & Science University, United States.
Aryana AbtinCasey Eye Institute, Oregon Health & Science University, United States.
Susan WentzienCasey Eye Institute, Oregon Health & Science University, United States.
Elizabeth WhiteCasey Eye Institute, Oregon Health & Science University, United States.
Diana C LozanoCasey Eye Institute, Oregon Health & Science University, United States.

Funding

Proteomics CoreP30EY010572 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI John Peter Campbell · 1995 to 2026
$19.4M
STUDIES IN GLAUCOMATOUS OPTIC NERVE DAMAGER01EY010145 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI MORRISON, JOHN C · 1993 to 2023
$8.9M
Modulation of optic nerve head astrocyte reactivity in glaucomaR01EY030429 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI LOZANO, DIANA DEL CARMEN, MORRISON, JOHN C · 2020 to 2024
$1.9M
NEI NIH HHS P30 EY010572NEI NIH HHS R01 EY010145NEI NIH HHS R01 EY030429
6 · The paper itself

Abstract

Animal models that help us understand how elevated intraocular pressure (IOP) causes axonal injury will lead to new glaucoma therapies. Because reliable measurements are difficult to obtain in chronic models, we developed the controlled elevation of IOP (CEI) approach. Here, a cannula connected to an elevated balanced salt solution (BSS) reservoir is inserted into the anterior chamber of anesthetized Brown Norway rats. The extent and duration of IOP exposure is controlled by adjusting the reservoir height. We now describe a method for creating CEI in awake animals. A Pinport, which has a silicone plug that can be penetrated repeatedly, is modified, attached to the skull, and connected to a microcannula that is implanted in the posterior chamber. To elevate IOP, BSS from a reservoir is allowed to flow through a pressure transducer to a swivel-mounted tether and injector. The injector is placed on the Pinport, bypassing the need for anterior chamber cannulation and general anesthesia during CEI. The surgical technique and equipment required for implantation are described, as well as the equipment and methods for performing awake CEI in several animals at a time. The ability of this system to control the level of IOP is demonstrated by TonoLab measurement, and by comparing reservoir (Pinport) pressures to direct measurement using an independent anterior chamber cannula and transducer. We also demonstrate that IOP elevation can be maintained over several hours. Specific pitfalls during and after surgical implantation are highlighted to help other researchers adopt these techniques.

Indexed as

Disease Models, AnimalIntraocular PressureOcular HypertensionAnimalsAnterior ChamberMaleRatsRats, Inbred BNTonometry, OcularWakefulness

Identifiers

PMID39805385
PMCPMC11824874

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Registered trials

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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.