Publication

Correspondence: Brian C. Samuels, ; bsamuels@uab.edu. PURPOSE. both model anatomy, anatomy purpose

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Last modified
  • 05/14/2025
Type of Material
Authors
    Jessica Jasien, University of Alabama BirminghamThomas A Read, Georgia Institute of TechnologyJoseph Van Batenburg-Sherwood, Imperial College LondonKristin M Perkumas, Duke UniversityChristopher Ethier, Emory UniversityDaniel W Stamer, Duke UniversityBrian C Samuels, University of Alabama Birmingham
Language
  • English
Date
  • 2022-01-01
Publisher
  • ASSOC RESEARCH VISION OPHTHALMOLOGY INC
Publication Version
Copyright Statement
  • 2022 The Authors
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 63
Issue
  • 1
Start Page
  • 21
End Page
  • 21
Grant/Funding Information
  • Supported by NIH/NEI grants R01 EY027759, EY030071, EY031710, EY028608 and EY022359, P30 EY003039, and both an unrestricted grant from Research to Prevent Blindness (RPB) to UAB as well as an RPB Physician-Scientist Award (Samuels).
Abstract
  • PURPOSE. Rodent and primate models are commonly used in glaucoma research; however, both have their limitations. The tree shrew (Tupaia belangeri) is an emerging animal model for glaucoma research owing in part to having a human-like optic nerve head anatomy, specifically a collagenous load-bearing lamina. However, the anterior segment anatomy and function have not been extensively studied in the tree shrew. Thus, the purpose of this study was to provide the first detailed examination of the anterior segment anatomy and aqueous outflow facility in the tree shrew. METHODS. Aqueous outflow dynamics were measured in five ostensibly normal eyes from three tree shrews using the iPerfusion system over a range of pressures. Gross histological assessment and immunohistochemistry were performed to characterize anterior segment anatomy and to localize several key molecules related to aqueous outflow. RESULTS. Anterior segment anatomy in tree shrews is similar to humans, demonstrating a scleral spur, a multilayered trabecular meshwork and a circular Schlemm's canal with a single lumen. Average outflow facility was 0.193 μL/min/mm Hg (95% confidence interval, 0.153-0.244), and was stable over time. Outflow facility was more similar between contralateral eyes (approximately 5% average difference) than between eyes of different animals. No significant dependence of outflow facility on time or pressure was detected (pressure-flow nonlinearity parameter of 0.01 (95% % confidence interval, -0.29 to 0.31 CI μL/min/mm Hg). CONCLUSIONS. These studies lend support to the usefulness of the tree shrew as a novel animal model in anterior segment glaucoma and pharmacology research. The tree shrew's cost, load-bearing collagenous lamina cribrosa, and lack of washout or anterior chamber deepening provides a distinct experimental and anatomic advantage over the current rodent and nonhuman primate models used for translational research.
Author Notes
  • Brian C. Samuels, Department of Ophthalmology and Visual Sciences, The University of Alabama at Birmingham School of Medicine, 1720 University Blvd, Birmingham, AL 35294, USA; Email: bsamuels@uab.edu
Keywords
Research Categories
  • Health Sciences, Opthamology
  • Engineering, Biomedical

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