May 2005
Volume 46, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2005
Heparan Mimetics (RGTA) Promote Corneal Wound Healing in vivo and in vitro
Author Affiliations & Notes
  • Y. Takesue
    Department of Ophthalmology, Fukuoka Univ Chikushi Hosp, Chikushino–shi, Japan
  • E. Huet
    CRRET/CNRS FRE 2412, Faculte des Sciences, Universite de Paris 12, Creteil Cedex, France
  • E. Gabison
    CRRET/CNRS FRE 2412, Faculte des Sciences, Universite de Paris 12, Creteil Cedex, France
    Fondation Ophtalmologique A. de Rothschild, Hopital Bichat, Paris, France
  • L. Racine
    Fondation Ophtalmologique A. de Rothschild, Hopital Bichat, Paris, France
  • T. Hoang–Xuan
    Fondation Ophtalmologique A. de Rothschild, Hopital Bichat, Paris, France
  • D. Barritault
    CRRET/CNRS FRE 2412, Faculte des Sciences, Universite de Paris 12, Creteil Cedex, France
  • J. Caruelle
    CRRET/CNRS FRE 2412, Faculte des Sciences, Universite de Paris 12, Creteil Cedex, France
  • S. Menashi
    CRRET/CNRS FRE 2412, Faculte des Sciences, Universite de Paris 12, Creteil Cedex, France
  • Footnotes
    Commercial Relationships  Y. Takesue, None; E. Huet, None; E. Gabison, None; L. Racine, None; T. Hoang–Xuan, None; D. Barritault, None; J. Caruelle, None; S. Menashi, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science May 2005, Vol.46, 2134. doi:
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      Y. Takesue, E. Huet, E. Gabison, L. Racine, T. Hoang–Xuan, D. Barritault, J. Caruelle, S. Menashi; Heparan Mimetics (RGTA) Promote Corneal Wound Healing in vivo and in vitro . Invest. Ophthalmol. Vis. Sci. 2005;46(13):2134.

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

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Abstract

Abstract: : Purpose: Regenerating Agent (RGTA) are heparan sulfate mimetics, that are known to stimulate tissue repair and reduce fibrosis wound healing in several models. We evaluated their activity in the cornea in vivo and in vitro. Methods: We assessed the effect of topical application of RGTA on corneal wound healing after alkali burn injury in C57BL6 mice. Slit–lamp examination, with fluorescein staining was performed on a daily basis after 1 N NaOH corneal injury. Epithelial defect, corneal opacity, and neovascularization were evaluated in a masked fashion. Corneal tissue sections were evaluated for inflammatory cell infiltration. In Vitro, cultured corneal epithelial cells were treated with RGTA or PBS as control to assess the effect of epithelial cell migration. Results: RGTA treated mice showed decreased corneal opacity as compared with non–treated group. Histological evaluation for inflammatory cell infiltration did not show any difference between both groups on days 3 after injury. RGTA treated corneal epithelial cells displayed enhanced migration rate as compared with PBS. Conclusions: Topical application of RGTA represents a new therapeutic approach in corneal injury. Further investigations are needed to assess the molecular events involved in this improved wound healing.

Keywords: wound healing • cornea: epithelium 
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