May 2004
Volume 45, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2004
Effect Of Human Amniotic Membrane (HAM) Treatment Upon Experimental Limbal Deficiency:clinical And Biochemical Analysis
Author Affiliations & Notes
  • J. Gomes
    Department of Ophthalmology, Vision Institute–Federal University of Sao Paulo/UNIFESP, Sao Paulo, Brazil
  • A. Lima
    Veterinary, University of Sao Paulo State /UNESP, Araçatuba, Brazil
  • M.Q. Campos
    Department of Ophthalmology, Vision Institute–Federal University of Sao Paulo/UNIFESP, Sao Paulo, Brazil
  • A.G. A. Berto
    Department of Biochemistry, Federal University of Sao Paulo/UNIFESP, Sao Paulo, Brazil
  • Y.M. Michelacci
    Department of Biochemistry, Federal University of Sao Paulo/UNIFESP, Sao Paulo, Brazil
  • Footnotes
    Commercial Relationships  J. Gomes, None; A. Lima, None; M.Q. Campos, None; A.G.A. Berto, None; Y.M. Michelacci, None.
  • Footnotes
    Support  none
Investigative Ophthalmology & Visual Science May 2004, Vol.45, 1429. doi:
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      J. Gomes, A. Lima, M.Q. Campos, A.G. A. Berto, Y.M. Michelacci; Effect Of Human Amniotic Membrane (HAM) Treatment Upon Experimental Limbal Deficiency:clinical And Biochemical Analysis . Invest. Ophthalmol. Vis. Sci. 2004;45(13):1429.

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

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Abstract

Abstract: : Purpose:The purpose of this study was to investigate the effects of HAM upon clinical and biochemical features of rabbit corneas submitted to limbal injury Methods: Right corneas of 20 rabbits underwent total peritomy and keratolimbectomy, followed by application of 0.5 M NaOH. Cryo–preserved HAM were sutured on the ocular surface of those eyes in ten animals (G1), and the right eyes of the remaining ten animals (G2) were kept uncovered. Normal contralateral eyes were used as matched controls at all groups. All animals were clinically evaluated everyday. At the 30th day, the rabbits were killed and both corneas were removed and sent for histopathological and biochemical analysis. Results:All animals presented with intense blepharospasm/photophobia, mucous secretion, and corneal neovascularization, but at the end of the experiment, the HAM–treated corneas presented less epithelial defects and cornea opacities were less severe than the untreated injured ones. Low molecular weight proteoglycans (PGs) of the lumican/decorin family were isolated from both control and experimental corneas and its concentration was reduced to a half in untreated injured corneas, and to 1/3 in the HAM–treated ones. Keratan sulfate (KS) and dermatan sulfate (DS) were identified as the main corneal glycosaminoglycans. The relative amounts of KS were very low in all injured corneas. The protein concentration was greatly increased in untreated injured corneas, but its concentration was equal to normal in the HAM–treated ones. Conclusions:Cryo–preserved HAM may be an effective alternative in ocular surface reconstructive surgery since the HAM–treated corneas demonstrated better clinical outcome and less epithelial defects. It seems that HAM had an inhibitory effect upon protein and PG biosynthesis. The HAM inhibitory effect upon PG and protein biosynthesis could allow the proper collagen organization, preventing corneal opacity. (CNPq, FAPESP, CAPES, SPDM)

Keywords: glycoconjugates/glycoproteins • cornea: basic science 
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