[Anti-scarring effect of rapamycin in rabbits following glaucoma filtering surgery]

Xin Kang1, Ying Shen1, Haixia Zhao1

  • 1Center of Myopia, Affiliated Hospital of Inner Mongolia Medical University, Hohhot 010050, China.

Abstract

Insights

Rapamycin eye drops reduced scarring after glaucoma surgery in rabbits by inhibiting fibroblast proliferation and promoting apoptosis. This treatment lowered intraocular pressure and reduced cell proliferation in filtering blebs.

Area of Science:

  • Ophthalmology
  • Pharmacology
  • Cell Biology

Background:

  • Glaucoma filtration surgery can lead to scarring, which impairs its long-term efficacy.
  • Fibroblast proliferation in the filtering bleb is a key factor in scar formation.
  • Rapamycin, an mTOR inhibitor, has shown anti-proliferative and pro-apoptotic effects.

Purpose of the Study:

  • To investigate the anti-scarring potential of rapamycin in a rabbit model of glaucoma filtration surgery.
  • To evaluate the effect of rapamycin on fibroblast proliferation and apoptosis in the filtering bleb.

Main Methods:

  • Trabeculectomy was performed on 96 rabbits, randomized into three rapamycin treatment groups (1%, 3%, 5%) and a control group.
  • Intraocular pressure (IOP) and inflammatory reactions were monitored; PCNA-positive cells in filtering blebs were quantified via immunohistochemistry.
  • Rabbit Tenon's capsule fibroblasts (RTFs) were cultured, and caspase expressions (caspase-3, -8, -9) were analyzed after rapamycin treatment.

Main Results:

  • Rapamycin treatment significantly reduced IOP and PCNA-positive cell counts in filtering blebs compared to controls (P < 0.05).
  • Rapamycin dose-dependently increased mRNA and protein expression of caspase-3 and caspase-9 (P < 0.001).
  • No significant changes in caspase-8 expression were observed with rapamycin treatment.

Conclusions:

  • Rapamycin effectively inhibits fibroblast proliferation and reduces scar formation following glaucoma filtration surgery in rabbits.
  • Rapamycin induces apoptosis of rabbit Tenon's capsule fibroblasts (RTFs) by upregulating caspase-3 and caspase-9 expression.

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