Therapeutic effects of three human-derived materials in a mouse corneal alkali burn model

Cutan Ocul Toxicol. 2019 Dec;38(4):315-321. doi: 10.1080/15569527.2019.1573244. Epub 2019 Jul 23.

Abstract

Purpose: To compare the therapeutic effects of human derivatives in a mouse alkali burn model. Methods: The right eyes of mice were injured using NaOH. After alkali injury, one of the following agents was topically administered for 7 d: human amniotic membrane (hAM) suspension, human umbilical cord serum (hUCS), and human peripheral blood serum (hPBS), or saline. The epithelial defect areas on days 1, 2, and 3 degrees of opacity on days 2, 3, and 7, and corneal neovascularization (NV) areas on day 7 were evaluated. Histologic examination and mRNA expression levels of tumour necrosis factor (TNF)-α, interleukin (IL)-6, vascular endothelial growth factor (VEGF), matrix metalloproteinase (MMP)-2, MMP-8, and MMP-9 were also evaluated on day 7. Results: The epithelial defect areas in the hUCS group were smaller than those in the control and hPBS groups on day 3 (p < .05, respectively). The epithelial defect areas in the hAM suspension group showed smaller than those in the control and hPBS groups on days 1 and 2 (p < .05, respectively). The degrees of opacity were lower in all treatment groups than that of the saline control group on day 7 (p < .05, respectively). Corneal NV areas were not different among groups on day 7 (p = 0.20). The expression levels of TNF-α, IL-6, MMP-8, and MMP-9 mRNA and the infiltration of the inflammatory cells in all treatment groups were lesser than those in the control group on day 7 (p< .05, respectively). Conclusions: All treatments reduced inflammatory reactions and corneal opacity development. Corneal reepithelialization was faster in the hUCS group.

Keywords: Alkali injury; amniotic membrane suspension; peripheral blood serum; umbilical cord serum.

MeSH terms

  • Amnion*
  • Animals
  • Burns, Chemical / pathology
  • Burns, Chemical / therapy*
  • Cornea / drug effects
  • Cornea / pathology
  • Corneal Neovascularization / pathology
  • Corneal Neovascularization / therapy*
  • Corneal Opacity / pathology
  • Corneal Opacity / therapy*
  • Eye Burns / chemically induced
  • Eye Burns / pathology
  • Eye Burns / therapy*
  • Humans
  • Male
  • Mice, Inbred BALB C
  • Serum*
  • Sodium Hydroxide / toxicity*

Substances

  • Sodium Hydroxide