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氯化十六烷基吡啶对兔角膜的电生理及解剖学影响。

Electrophysiological and anatomical effects of cetylpyridinium chloride on the rabbit cornea.

作者信息

Green K

出版信息

Acta Ophthalmol (Copenh). 1976 Apr;54(2 p):145-59. doi: 10.1111/j.1755-3768.1976.tb00426.x.

Abstract

The effects of cetylpyridinium chloride on the trans-corneal potential difference and the surface anatomy of the cornea have been examined. Concentrations of cetylpyridinium chloride from 0.21 mM to 2 mM were used for either 1 or 2 minute exposure times on the in vitro and in vivo cornea for the electrophysiology studies. The potential difference of the in vitro cornea showed a concentration and exposure-time dependent decrease, the in vivo cornea shows a qualitatively similar behaviour although quantitatively less. The fall in potential difference is preceeded by a hyperpolarization. The scanning electromicroscopy reveals a loss of microvilli and microplicae as well as surface pitting, with some exposure of cells underlying the superficial epithelium. These changes occur in a dose-dependent manner. The effect of cetylpyridinium chloride on the cornea is to enhance the permeability of the superficial cells by destroying the cell membranes and causing lysis of the cells.

摘要

已研究了氯化十六烷基吡啶对跨角膜电位差和角膜表面解剖结构的影响。在体外和体内角膜的电生理研究中,使用浓度为0.21 mM至2 mM的氯化十六烷基吡啶,暴露时间为1或2分钟。体外角膜的电位差呈现出浓度和暴露时间依赖性降低,体内角膜表现出定性相似的行为,尽管在数量上较少。电位差下降之前有超极化现象。扫描电子显微镜显示微绒毛和微褶消失以及表面麻点,浅表上皮下方的细胞有一些暴露。这些变化呈剂量依赖性发生。氯化十六烷基吡啶对角膜的作用是通过破坏细胞膜并导致细胞裂解来增强浅表细胞的通透性。

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