May 2005
Volume 46, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2005
Characterization of Effects of Systemic Antibiotics in a Rat Model of Retinal Detachment
Author Affiliations & Notes
  • S.I. Pachydaki
    Retina Service,
    Massachusetts Eye & Ear Infirmary, Boston, MA
  • L. Sobrin
    Retina Service,
    Massachusetts Eye & Ear Infirmary, Boston, MA
  • T. Nakazawa
    Retina Service,
    Massachusetts Eye & Ear Infirmary, Boston, MA
  • C.L. Grosskreutz
    Glaucoma Service,
    Massachusetts Eye & Ear Infirmary, Boston, MA
  • D.N. Zacks
    Retina Service, Kellogg Eye Center, Ann Arbor, MI
  • J.W. Miller
    Retina Service,
    Massachusetts Eye & Ear Infirmary, Boston, MA
  • Footnotes
    Commercial Relationships  S.I. Pachydaki, None; L. Sobrin, None; T. Nakazawa, Massachusetts Eye & Ear Infirmary P; C.L. Grosskreutz, None; D.N. Zacks, Massachusetts Eye & Ear Infirmary P; J.W. Miller, Massachusetts Eye & Ear Infirmary P.
  • Footnotes
    Support  Harvard Medical School Dept of Ophthalmology Joint Clinical Research Center Pilot Project Grant
Investigative Ophthalmology & Visual Science May 2005, Vol.46, 5572. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      S.I. Pachydaki, L. Sobrin, T. Nakazawa, C.L. Grosskreutz, D.N. Zacks, J.W. Miller; Characterization of Effects of Systemic Antibiotics in a Rat Model of Retinal Detachment . Invest. Ophthalmol. Vis. Sci. 2005;46(13):5572.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract

Abstract: : Purpose: Antibiotics are widely used during and after retinal detachment repair. The purpose of this experiment is to characterize the effects of ampicillin, ofloxacin, ceftriaxone, and fosfomycin on photoreceptor apoptosis in a rat model of retinal detachment. Methods: Retinal detachments were created in Brown Norway rats by injecting 10% hyaluronic acid into the subretinal space using a transvitreous approach. Ampicillin (100 mg/kg/day), ofloxacin (6 mg/kg/day), ceftriaxone (50 mg/kg/day), and fosfomycin (20 mg/kg/day) were injected intraperitoneally on the day of detachment induction and for the two following days (n = 6 eyes for each antibiotic). Control animals received saline intraperitoneal injections on the day of detachment induction and for the two following days (n = 6 eyes). All eyes were enucleated 72 hours after retinal detachment induction, embedded in paraffin and sectioned every 6 µm. Light microscopy and terminal dUTP–biotin nick end–labeling (TUNEL) was performed to assay for morphologic features associated with apoptosis. TUNEL–positive cells were counted by a masked observer. The mean number of TUNEL–positive cells was determined by averaging the number of TUNEL–positive cells in three sections of each eye. Results:Light microscopic analysis of detached retinas showed the presence of pyknotic nuclei in the outer nuclear layer and disruption of the normal organization of the photoreceptor outer segments. TUNEL–staining was positive in the outer nuclear layer only in the detached portions of retina. The mean number of TUNEL–positive cells was greater in control eyes (mean ± SD, 86.2 ± 34.3) vs. eyes of animals treated with ampicillin (54.1 ± 25.5), ofloxacin (49.4 ± 21.1), ceftriaxone (37.4 ± 13.8), and fosfomycin (56.5 ± 42.2). However, these differences were statistically significant for ofloxacin and ceftriaxone (p = 0.05 and 0.009, respectively) but not for ampicillin or fosfomycin (p = 0.10 and 0.21, respectively). Conclusions: These preliminary data suggest that systemic administration of the antibiotics ofloxacin and ceftriaxone may decrease photoreceptor apoptosis associated with retinal detachment.

Keywords: retinal detachment • apoptosis/cell death • antibiotics/antifungals/antiparasitics 
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×