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纳豆激酶(枯草杆菌蛋白酶NAT)诱导的玻璃体后脱离:一种用于药物性玻璃体溶解的新型酶。

Posterior vitreous detachment induced by nattokinase (subtilisin NAT): a novel enzyme for pharmacologic vitreolysis.

作者信息

Takano Akiomi, Hirata Akira, Ogasawara Kazuya, Sagara Nina, Inomata Yasuya, Kawaji Takahiro, Tanihara Hidenobu

机构信息

Department of Ophthalmology and Visual Science, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan.

出版信息

Invest Ophthalmol Vis Sci. 2006 May;47(5):2075-9. doi: 10.1167/iovs.05-0130.

Abstract

PURPOSE

To investigate the effects of intravitreal injection of nattokinase (subtilisin NAT), a serine protease that is produced by Bacillus subtilis (natto), for induction of posterior vitreous detachment (PVD).

METHODS

Different doses of nattokinase (1, 0.1, or 0.01 fibrin-degradation units [FU]) or physiologic saline as a control were injected into the vitreous cavity of rabbit eyes. Scanning electron microscopy was used to observe the retinal surfaces of four rabbit eyes per concentration. Histologic alterations were assessed by light microscopy, using four eyes from each group. Electroretinography (ERG) was performed to observe retinal function, ranging from 1 hour to 1 week after the nattokinase (1 or 0.1 FU) or saline solution administration, using four eyes from each group at each time point. Also, findings in all rabbits were monitored by slit lamp examination and by indirect ophthalmoscopy with a 20-D lens.

RESULTS

Scanning electron microscopy showed smooth retinal surfaces, indicating the occurrence of PVD at 30 minutes after intervention in all the experimental eyes injected with 0.1 or 1.0 FU nattokinase, but none of the control eyes. Light microscopy and ERG analysis showed no critical change even after the use of 0.1 FU nattokinase, an amount sufficient to induce PVD. However, toxicity in the forms of preretinal hemorrhage and ERG changes was noted with the higher dose (1 FU) of nattokinase.

CONCLUSIONS

The results suggested that nattokinase is a useful enzyme for pharmacologic vitreolysis because of its efficacy in inducing PVD.

摘要

目的

研究玻璃体内注射纳豆激酶(枯草杆菌蛋白酶NAT,一种由枯草芽孢杆菌(纳豆)产生的丝氨酸蛋白酶)诱导玻璃体后脱离(PVD)的效果。

方法

将不同剂量的纳豆激酶(1、0.1或0.01纤维蛋白降解单位[FU])或作为对照的生理盐水注入兔眼玻璃体腔。使用扫描电子显微镜观察每个浓度下四只兔眼的视网膜表面。每组取四只眼,通过光学显微镜评估组织学改变。在注射纳豆激酶(1或0.1 FU)或生理盐水后1小时至1周内,每组每次取四只眼进行视网膜电图(ERG)检查以观察视网膜功能。此外,通过裂隙灯检查和使用20D透镜的间接检眼镜对所有兔子的情况进行监测。

结果

扫描电子显微镜显示视网膜表面光滑,表明在所有注射0.1或1.0 FU纳豆激酶的实验眼中,干预后30分钟出现了PVD,而对照眼中均未出现。光学显微镜和ERG分析显示,即使使用足以诱导PVD的0.1 FU纳豆激酶后,也未发现严重变化。然而,较高剂量(1 FU)的纳豆激酶出现了视网膜前出血和ERG变化等毒性表现。

结论

结果表明,纳豆激酶因其诱导PVD的功效,是一种用于药物性玻璃体溶解的有用酶。

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