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逍生散对干眼杯状细胞影响的实验研究

祁怡馨 谢立科 郝晓凤 张志芳 侯乐 肖文峥 孙会兰 明镜

北京中医药大学学报2017,Vol.40Issue(4):302-307,327,7.
北京中医药大学学报2017,Vol.40Issue(4):302-307,327,7.DOI:10.3969/j.issn.1006-2157.2017.04.008

逍生散对干眼杯状细胞影响的实验研究

Effects of Xiaosheng San on goblet cells of dry eyes in mice: a laboratory study

祁怡馨 1谢立科 1郝晓凤 1张志芳 1侯乐 1肖文峥 1孙会兰 1明镜1

作者信息

  • 1. 中国中医科学院眼科医院 北京 100040
  • 折叠

摘要

Abstract

Objective To study the effects of Xiaosheng San(XSS, Xiaosheng Granules) on goblet cells of dry eyes in mice and evaluate its mechanism.Methods 180 male C57BL/6 mice were divided into six groups: normal control (group A), model (group B), saline (group C), XSS low-dose (group D), XSS medium-dose (group E) and high-dose (group F) groups.Dry eye model was established by injecting scopolamine subcutaneously at the base of rear legs in all groups except normal control group.Schirmer I test (SIT), tear break-up time (BUT),corneal fluorescent (FL) staining, and the number of conjunctival goblet cells before and after modeling, and at four weeks after intervention were measured.Results BUT, SIT,and number of goblet cells in group B, C, D, E,and F were significantly decreased after scopolamine treatment(P<0.05), while no significant difference (P>0.05) was found in group A.FL were significantly increased after model establishment (P<0.05).Medium-and high-dose XSS significantly improved SIT, BUT and the number of goblet cells in group E and F (P<0.05).No such changes were observed in group A, B and C (P>0.05).Conclusion Subcutaneous injecfion of scopolamine could effectively establish dry eye model in mice.Xiaosheng Granules could increase tear secretion, prolong tear break-up time, improve stability, inhibit apoptosis of goblet cells and reduce injury to eye surface.

关键词

逍生散/干眼/杯状细胞/小鼠

Key words

xiaoshengsan/dry eye/goblet cells/mice

分类

医药卫生

引用本文复制引用

祁怡馨,谢立科,郝晓凤,张志芳,侯乐,肖文峥,孙会兰,明镜..逍生散对干眼杯状细胞影响的实验研究[J].北京中医药大学学报,2017,40(4):302-307,327,7.

基金项目

国家自然科学基金资助项目(No.81273805),北京市科学技术委员会项目(No.Z141100002214001) (No.81273805)

北京中医药大学学报

OA北大核心CSCDCSTPCD

1006-2157

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