AI Article Synopsis

  • A rabbit model for posterior penetrating eye injury was developed to assess potential therapies for retinal fibrosis.
  • Rabbits were studied at various time points after injury, with early signs of fibrosis observed by Day 14 and more severe fibrosis noted by Day 28.
  • The findings indicate that ocular fibrosis can develop rapidly after injury, helping to identify key timeframes for future treatment research.

Article Abstract

Introduction: To establish a rabbit model of posterior penetrating eye injury as a platform to test potential therapeutics.

Materials And Methods: Anesthetized rabbits received posterior penetrating eye injury in one eye, whereas contralateral eyes were maintained as uninjured controls. Rabbits were randomized into two experimental groups. Group A was euthanized on Day 14 postinjury to determine retinal fibrosis at an early phase of disease progression. Group B was euthanized on Day 28 postinjury to examine retinal fibrosis at a late phase of disease progression. We examined animals on postinjury Days 7, 14, 21, and 28 with indirect ophthalmoscope and fundus photography. After euthanasia, eyes were processed for histology and immunofluorescence labeling of fibrotic proteins α-smooth muscle actin and collagen I.

Results: Early fibrosis was detected by Day 14, as indicated by indirect ophthalmoscopy and fundus imaging. Fibrotic membranes were visible at sites of injury. Immunofluorescence analysis detected α-smooth muscle actin and collagen I within the fibrotic membranes.

Conclusions: These data show that ocular fibrosis can be detected within 14 days after initial injury, with more severe fibrosis detected at 28 days postinjury. These results will be used to determine the optimal time points for later studies designed to test treatment strategies.

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Source
http://dx.doi.org/10.1093/milmed/usz221DOI Listing

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