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醛糖还原酶抑制剂可对抗基质金属蛋白酶-10的表达增强,并改善半乳糖喂养大鼠的角膜伤口愈合。

Aldose reductase inhibitor counteracts the enhanced expression of matrix metalloproteinase-10 and improves corneal wound healing in galactose-fed rats.

作者信息

Takamura Yoshihiro, Matsumoto Takafumi, Tomomatsu Takeshi, Matsumura Takehiro, Takihara Yuji, Inatani Masaru

机构信息

Department of Ophthalmology, Faculty of Medical Sciences, University of Fukui, Eiheiji-cho, Yoshida-gun, Fukui, Japan.

出版信息

Mol Vis. 2013 Dec 8;19:2477-86. eCollection 2013.

Abstract

PURPOSE

We investigated the effect of an aldose reductase inhibitor (ARI) and the role of matrix metalloproteinase (MMP)-10 on recovery after corneal epithelium removal in a rat diabetic keratopathy model.

METHODS

Three-week-old Sprague-Dawley rats were fed the following diets for 6 weeks: normal MF chow (MF), 50% galactose (Gal), and 50% Gal containing 0.01% ARI (Gal +ARI). The corneal epithelium was removed using n-heptanol, and the area of epithelial defects was photographed and measured every 24 h. Real-time reverse transcriptase PCR, western blotting, and immunohistochemistry were used to determine the expression profile of MMP-10 and integrin α3.

RESULTS

Compared to the MF control group, the amount of galactitol in the Gal group increased approximately 200-fold, which was reduced to sevenfold by ARI treatment. The area of corneal erosion in the Gal group was significantly larger than in the MF group at 72 h and thereafter (p<0.01, unpaired t test). The expression level of MMP-10 was enhanced at both the protein and mRNA levels by exposure to a high concentration of Gal, while integrin α3 expression decreased at the protein level but remained unchanged at the mRNA level. Delayed epithelial wound healing and alterations in the expression levels of MMP-10 and integrin α3 were normalized by ARI. The corneal erosion closure rate was significantly decreased with topical recombinant MMP-10.

CONCLUSIONS

These studies confirm that the increased expression of MMP-10 induced by Gal feeding is counteracted by ARI treatment and suggest a role of MMP-10 in modulating corneal epithelial wound healing.

摘要

目的

我们在大鼠糖尿病角膜病变模型中研究了醛糖还原酶抑制剂(ARI)的作用以及基质金属蛋白酶(MMP)-10在角膜上皮去除后恢复过程中的作用。

方法

给3周龄的Sprague-Dawley大鼠喂食以下饮食6周:正常MF饲料(MF)、50%半乳糖(Gal)和含0.01% ARI的50% Gal(Gal +ARI)。使用正庚醇去除角膜上皮,每24小时拍摄并测量上皮缺损面积。采用实时逆转录聚合酶链反应、蛋白质印迹法和免疫组织化学法测定MMP-10和整合素α3的表达谱。

结果

与MF对照组相比,Gal组的半乳糖醇含量增加了约200倍,经ARI治疗后降至7倍。Gal组角膜糜烂面积在72小时及之后显著大于MF组(p<0.01,非配对t检验)。暴露于高浓度Gal后,MMP-10在蛋白质和mRNA水平的表达均增强,而整合素α3在蛋白质水平表达下降,但在mRNA水平保持不变。ARI使上皮伤口愈合延迟以及MMP-10和整合素α3表达水平的改变恢复正常。局部应用重组MMP-10可显著降低角膜糜烂闭合率。

结论

这些研究证实,Gal喂养诱导的MMP-10表达增加可被ARI治疗抵消,并提示MMP-10在调节角膜上皮伤口愈合中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b578/3857161/d28938df6357/mv-v19-2477-f1.jpg

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