TY - JOUR
T1 - Effects of amniotic membrane suspension in the rat alkali burn model
AU - Choi, Jin A.
AU - Choi, Jun Sub
AU - Joo, Choun Ki
PY - 2011
Y1 - 2011
N2 - Purpose: The main objective of this study is to determine the anti-inflammatory effect of topical amniotic membrane (AM) suspension on corneal alkali burn compared to topical serum eyedrops. Methods: Thirty eyes from 30 Sprague-Dawley male rats were used. After alkali injuries using 1 N NaOH, the control group (n=10) received topical PBS four times a day for 2 days. The first study group received topical 30% AM suspension, and the second study group (n=10) received topical 30% rat serum. Using slit lamp biomicroscopy, injured corneas were evaluated and scored in terms of re-epithelialization, corneal opacity, and neovascularization (NV). Tissue sections were analyzed histologically for cellular infiltration, and immunohistochemical staining was conducted using rat anti-mouse F4/80 antibody for the detection of macrophages. Results: In the inflammatory wound healing model, the epithelial healing ratios of the control group, the AM suspension group, and the serum eyedrop group were 1.8±15.1%, 34.1±17.7%, and 41.5±16.1%, respectively (p<0.0001). The opacity scores for the control group, the AM suspension group, and the serum eyedrop group 48 h after the insult were 4.8±0.5, 3.4±0.5, and 3.0±0.8, respectively, showing a significant difference (p<0.0001). Moreover, the NV scores for the control group, AM suspension group, and serum eyedrop group 48 h after the insult were 5.8±0.9, 4.0±1.3, and 4.3±0.9 (p=0.006). Upon immunohistochemical evaluation using F4/80, significantly fewer F4/80+ cells were recruited in the AM suspension and serum eyedrop groups than the control group (p=0.027). Conclusions: The suspension form of the amniotic membrane promoted epithelial healing and reduced corneal opacity and NV in alkali burn. It also suppressed F4/80 expression in the corneal stroma, indicating that the AM suspension maintains its beneficial biochemical effect on inflammatory corneal wound healing in vivo.
AB - Purpose: The main objective of this study is to determine the anti-inflammatory effect of topical amniotic membrane (AM) suspension on corneal alkali burn compared to topical serum eyedrops. Methods: Thirty eyes from 30 Sprague-Dawley male rats were used. After alkali injuries using 1 N NaOH, the control group (n=10) received topical PBS four times a day for 2 days. The first study group received topical 30% AM suspension, and the second study group (n=10) received topical 30% rat serum. Using slit lamp biomicroscopy, injured corneas were evaluated and scored in terms of re-epithelialization, corneal opacity, and neovascularization (NV). Tissue sections were analyzed histologically for cellular infiltration, and immunohistochemical staining was conducted using rat anti-mouse F4/80 antibody for the detection of macrophages. Results: In the inflammatory wound healing model, the epithelial healing ratios of the control group, the AM suspension group, and the serum eyedrop group were 1.8±15.1%, 34.1±17.7%, and 41.5±16.1%, respectively (p<0.0001). The opacity scores for the control group, the AM suspension group, and the serum eyedrop group 48 h after the insult were 4.8±0.5, 3.4±0.5, and 3.0±0.8, respectively, showing a significant difference (p<0.0001). Moreover, the NV scores for the control group, AM suspension group, and serum eyedrop group 48 h after the insult were 5.8±0.9, 4.0±1.3, and 4.3±0.9 (p=0.006). Upon immunohistochemical evaluation using F4/80, significantly fewer F4/80+ cells were recruited in the AM suspension and serum eyedrop groups than the control group (p=0.027). Conclusions: The suspension form of the amniotic membrane promoted epithelial healing and reduced corneal opacity and NV in alkali burn. It also suppressed F4/80 expression in the corneal stroma, indicating that the AM suspension maintains its beneficial biochemical effect on inflammatory corneal wound healing in vivo.
UR - https://www.scopus.com/pages/publications/79952159984
M3 - Article
C2 - 21311604
AN - SCOPUS:79952159984
SN - 1090-0535
VL - 17
SP - 404
EP - 412
JO - Molecular Vision
JF - Molecular Vision
ER -