Short-Term Response of Mitomycin C on the Human Rectus Muscle Following Strabismus Surgery: Histological, Ultrastructural, and Biomechanical Evaluation

被引:7
作者
Choi, Samjin [1 ,2 ,3 ]
Cheong, Youjin [1 ,2 ]
Shin, Jae-Ho [4 ]
Kim, Kyung A. [3 ]
Bang, Jae Beum [5 ]
Jin, Kyung-Hyun [4 ]
Park, Hun-Kuk [1 ,2 ,6 ]
机构
[1] Kyung Hee Univ, Dept Biomed Engn, Seoul, South Korea
[2] Kyung Hee Univ, Healthcare Ind Res Inst, Seoul, South Korea
[3] Kyung Hee Univ, Dept Orthodont, Seoul, South Korea
[4] Kyung Hee Univ, Dept Ophthalmol, Seoul, South Korea
[5] Kyung Hee Univ, Dept Dent Educ, Seoul, South Korea
[6] Kyung Hee Univ, Dept Med Engn, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
mitomycin C (MMC); human rectus muscles; collagen fibrils; nanostructural and biomechanical properties; inflammation;
D O I
10.1017/S1431927612013840
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
This study investigated the inflammatory effect of intraoperative mitomycin C (MMC) on adhesion reformation in human rectus muscles. Ten consecutive patients who underwent medial rectus resection had their postoperative rectus muscles divided into two groups: control group (n = 10) and MMC group (n = 10). In the MMC group, the muscle was soaked for 2 min with MMC, prepared as a 0.2 mg/mL (0.02%) solution. The 0.02% MMC reactions were examined using histological analysis with hematoxylin-eosin (inflammatory response) and Masson's trichrome (collagen fibrils), immunoreactivities of cyclooxygenase-II (inflammatory response), and collagen type I and III, scanning electron microscopy analysis to quantify the diameter and D-periodicity of collagen fibrils, and atomic force microscopy analysis to quantify the diameter, D-periodicity, and adhesion force of collagen fibrils. The rectus muscles treated with 0.02% MMC showed a significantly increased inflammatory response (p < 0.05), increased collagen density (p < 0.0001), increased fibril diameter (p < 0.001 or p < 0.05), and decreased fibril adhesion force (p < 0.005) compared to the rectus muscles in the control group. MMC simultaneously caused an inflammatory response as well as nanostructural and biomechanical property changes in the collagen fibril network.
引用
收藏
页码:227 / 232
页数:6
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