Duan Hai-Xia, Guan Huai-Jin, Yang Ling, Xu Xue-Dong, Zou Mei-Bo
Ophthalmic Center, the Affiliated Hospital of Nantong University, Nantong, China.
Zhonghua Yan Ke Za Zhi. 2007 Oct;43(10):917-21.
To assess whether preservative-free 1% lidocaine is capable of loosing the junction between the rabbit lens epithelial cells (LECs) and between the cells and capsules and is capable of destroying the LECs, in order to provide scientific basis for pursuing safe and effective drugs to eliminate LECs in cataract surgery and to prevent capsular pacification.
Lens capsule specimens were collected from 29 rabbits (58 eyes) and divided into 3 groups: balanced salt solution (BSS) group (exposed to BSS for 1 minute), lidocaine group (exposed to preservative-free 1% lidocaine for 1 minute) and the control group. Specimens were stained with trypan blue and alizarin red. Photomicrographs of each capsule were taken to observe the viability of LECs and count the number of dead LECs. The histopathologic changes of LECs treated with lidocaine were evaluated by histological method and transmission electron microscope.
The rate of dead LECs of the anterior and the equatorial lens capsules in control group was (1.51 +/- 0.39)%, and (1.52 +/- 0.32)%, respectively. The rate of dead LECs of the anterior and the equatorial lens capsules irrigated with BSS was (1.78 +/- 0.50)% and (1.77 +/- 0.47)%. The rate of dead LECs of the anterior and the equatorial lens capsules irrigated with preservative-free 1% lidocaine was (13.01 +/- 4.67)% and (9.59 +/- 3.35)%, respectively. The nested design ANOVA showed that the rate of dead LECs in the lidocaine group was greater than that in the control group or BSS group (P < 0.05), There was no significant difference in the number of dead cells between the anterior lens capsules and the equatorial lens capsules. After irrigated with lidocaine, cavities appeared ibetween the LECs and the capsule, cells detached from the capsule and showed vacuoles. The capsules of control group and BSS group showed a normal layer of LECs attached to the capsule. Under transmission electron microscope, in the lidocaine group, the junction between LECs and between the cell and the capsule were destroyed, many cells detached from the capsule and the rest arranged loosely. Some LECs dentes, and many vacuoles emerged, resulting in destruction of the cellular frame.
Preservative-free 1% lidocaine may loose the junction between the LECs and between the cells and capsules, resulting in degeneration and death of the LECs.
评估不含防腐剂的1%利多卡因是否能够松解兔晶状体上皮细胞(LECs)之间以及细胞与囊膜之间的连接,并能否破坏LECs,为寻求安全有效的药物以消除白内障手术中的LECs并预防囊膜皱缩提供科学依据。
从29只兔(58只眼)收集晶状体囊膜标本,分为3组:平衡盐溶液(BSS)组(暴露于BSS 1分钟)、利多卡因组(暴露于不含防腐剂的1%利多卡因1分钟)和对照组。标本用台盼蓝和茜素红染色。对每个囊膜拍摄显微照片以观察LECs活力并计数死亡LECs数量。通过组织学方法和透射电子显微镜评估利多卡因处理后LECs的组织病理学变化。
对照组前囊膜和赤道部囊膜的LECs死亡率分别为(1.51±0.39)%和(1.52±0.32)%。用BSS冲洗的前囊膜和赤道部囊膜的LECs死亡率分别为(1.78±0.50)%和(1.77±0.47)%。用不含防腐剂的1%利多卡因冲洗的前囊膜和赤道部囊膜的LECs死亡率分别为(13.01±4.67)%和(9.59±3.35)%。嵌套设计方差分析显示利多卡因组的LECs死亡率高于对照组或BSS组(P<0.05),前囊膜和赤道部囊膜的死亡细胞数量无显著差异。用利多卡因冲洗后,LECs与囊膜之间出现腔隙,细胞从囊膜脱离并出现空泡。对照组和BSS组的囊膜显示有一层正常的LECs附着于囊膜。在透射电子显微镜下,利多卡因组中,LECs之间以及细胞与囊膜之间的连接被破坏,许多细胞从囊膜脱离,其余细胞排列松散。一些LECs出现凹陷,出现许多空泡,导致细胞结构破坏。
不含防腐剂的1%利多卡因可能松解LECs之间以及细胞与囊膜之间的连接,导致LECs变性和死亡。