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经紫外线 A/核黄素角膜交联术后角膜胶原纤维变化。

Corneal collagen fibril changes after ultraviolet a/riboflavin corneal crosslinking.

机构信息

Department of Ophthalmology, PLA Navy General Hospital, Beijing, China.

出版信息

Cornea. 2014 Jan;33(1):56-9. doi: 10.1097/ICO.0000000000000017.

DOI:10.1097/ICO.0000000000000017
PMID:24240489
Abstract

PURPOSE

The aim was to investigate the changes in collagen type 1 and type 3 in rabbit corneas undergoing corneal crosslinking with ultraviolet A and riboflavin and to analyze the possible mechanisms of corneal haze formation.

METHODS

After removal of the central epithelium, the right corneas of 60 New Zealand rabbits were crosslinked with riboflavin and ultraviolet A, and 10 additional rabbits were used as the control group. The animals were killed 3, 7, 15, 30, 90, and 180 days postoperatively. Collagen type 1 and type 3 were analyzed using picrosirius red stain by means of polarized light microscopy. The biochemical changes in collagen type 3 at the time points indicated above were determined by Western blot analyses.

RESULTS

Collagen type 3 was significantly increased 30 days after corneal crosslinking compared with that in the control cornea, gradually increased until reaching its maximum value 90 days after riboflavin and ultraviolet A crosslinking, and then decreased until it returned to the normal state 180 days after crosslinking. There were no significant changes in collagen type 1 over time after corneal crosslinking. In agreement with the picrosirius red staining results, the western blot analyses showed that collagen type 3 was detected 15 days after the crosslinking treatment and continued to be present. However, 180 days after the crosslinking treatment, collagen type 3 could not be found in the crosslinked corneas.

CONCLUSIONS

These findings suggest that ultraviolet A/riboflavin crosslinking results in collagen type 3 synthesis and degradation, which may offer at least a partial explanation for the formation of corneal haze.

摘要

目的

本研究旨在探讨兔眼角膜经紫外线 A 和核黄素交联治疗后Ⅰ型和Ⅲ型胶原的变化,并分析角膜混浊形成的可能机制。

方法

去除中央上皮后,用核黄素和紫外线 A 对 60 只新西兰兔的右眼角膜进行交联,另外 10 只兔作为对照组。术后 3、7、15、30、90 和 180 天处死动物。采用偏振光显微镜下的苦味酸天狼猩红染色法分析Ⅰ型和Ⅲ型胶原。采用 Western blot 分析在上述时间点检测到的Ⅲ型胶原的生化变化。

结果

与对照组相比,角膜交联后 30 天Ⅲ型胶原显著增加,直到核黄素和紫外线 A 交联后 90 天达到最大值,然后逐渐减少,直到交联后 180 天恢复正常状态。角膜交联后Ⅰ型胶原随时间无明显变化。与苦味酸天狼猩红染色结果一致,Western blot 分析显示交联处理后 15 天即可检测到Ⅲ型胶原,且持续存在。然而,交联后 180 天,交联角膜中无法检测到Ⅲ型胶原。

结论

这些发现表明,紫外线 A/核黄素交联导致Ⅲ型胶原的合成和降解,这至少可以部分解释角膜混浊的形成。

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