Triamcinolone acetonide decreases outflow facility in C57BL/6 mouse eyes

Invest Ophthalmol Vis Sci. 2013 Feb 1;54(2):1280-7. doi: 10.1167/iovs.12-11223.

Abstract

Purpose: To determine the effect of triamcinolone acetonide (TA) on outflow facility in mice.

Methods: Animals received 20 μL of TA (40 mg/mL) suspension subconjunctivally either bilaterally or unilaterally and were euthanized after either 1 week or 3 weeks. Before mice were killed, IOP was measured with a rebound tonometer. Outflow facility was determined using simultaneous pressure and flow measurements. Another set of animals received bilateral injection of anecortave acetate (AA) with or without bilateral TA injection and their outflow facility was also determined. Myocilin expression was investigated in a subset of eyes using quantitative PCR (qPCR).

Results: Outflow facility of eyes in animals receiving bilateral TA injection (TA(BL)) and TA-treated eyes of animals receiving unilateral injection (TA(UL)) was significantly decreased compared to naïve control eyes (C(naive)) after 1 week and 3 weeks of TA treatment (ANOVA P < 0.01, P < 0.001, respectively). Eyes treated with AA (with or without TA) had higher outflow facility than animals treated with TA (P < 0.05). IOP data did not show any significant difference between groups. qPCR analysis revealed significant decrease in myocilin expression in eyes receiving AA compared to naïve control and TA-treated eyes (ANOVA P < 0.001).

Conclusions: Steroid treatment significantly decreases outflow facility in C57BL/6 mice despite having small effect on IOP. This animal model can be useful for studying the pathogenesis of steroid-induced glaucoma.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism
  • Disease Models, Animal*
  • Eye Proteins / genetics
  • Eye Proteins / metabolism
  • Female
  • Glaucoma / chemically induced*
  • Glaucoma / metabolism*
  • Glucocorticoids / toxicity*
  • Glycoproteins / genetics
  • Glycoproteins / metabolism
  • Hydrocortisone / analogs & derivatives
  • Hydrocortisone / toxicity
  • Intraocular Pressure / drug effects
  • Intraocular Pressure / physiology
  • Mice
  • Mice, Inbred C57BL*
  • Microdialysis / methods
  • Models, Biological
  • RNA, Messenger / metabolism
  • Trabecular Meshwork / drug effects
  • Trabecular Meshwork / metabolism
  • Triamcinolone Acetonide / toxicity*

Substances

  • Cytoskeletal Proteins
  • Eye Proteins
  • Glucocorticoids
  • Glycoproteins
  • RNA, Messenger
  • trabecular meshwork-induced glucocorticoid response protein
  • Triamcinolone Acetonide
  • Anecortave
  • Hydrocortisone