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[缺氧后角膜黄素蛋白的氧化还原荧光测定研究。初步结果]

[Redox fluorometry study of corneal flavoproteins following hypoxia. Preliminary results].

作者信息

Raynaud C, Coulangeon L M, Sole P, Coudert J

机构信息

Service d'Ophtalmologie, CHU G. Montpied, Clermont-Ferrand.

出版信息

J Fr Ophtalmol. 1995;18(5):347-55.

PMID:7560770
Abstract

PURPOSE

The cornea is frequently associated to hypoxia, whether during residence in the heights or more often when wearing contact lenses. To evaluate the corneal modifications induced by hypoxia at an infraclinical stage, we have used redox fluorometry that enables to study in vivo the metabolic response of the cells while measuring the fluorescence of the flavoproteins (FAD) of the corneal cells.

METHODS

The variations of the corneal fluorescence were studied in 12 healthy subjects, before and after a topically-induced 5-minute corneal hypoxia, submitting 2 eyes to a prehumidified flow of nitrogen 100%. The results were compared to those found in the same subjects after exposure under the same conditions to an ambiant air flow (N2 = 69%; O2 = 21%). The measurements of the corneal fluorescence were carried out with the fluorophotometre Flurotron Master FM2.

RESULTS

The authors did not find any statistically significant difference in the corneal fluorescence between the right and the left eyes of these 12 subjects, whether under normal conditions, under hypoxia, or under air flow (wilcoxon T-test, Friedman test).

CONCLUSION

As there are no significant results, these authors suggest that the chosen exposure time, although sufficient in vitro to induce a modification of the fluorecence of the cellular flavoproteins, may be too "short" in vivo. The use of complementary filters with the FM2 system would yield more information. The study of these results led the authors to broaden their search whether by looking for conditions for general hypoxia (hypobarric box) or by increasing local hypoxia (contact lenses).

摘要

目的

角膜经常与缺氧相关,无论是在高海拔地区停留期间,还是更常见的佩戴隐形眼镜时。为了评估亚临床阶段缺氧诱导的角膜变化,我们使用了氧化还原荧光测定法,该方法能够在体内研究细胞的代谢反应,同时测量角膜细胞黄素蛋白(FAD)的荧光。

方法

在12名健康受试者中,研究了局部诱导的5分钟角膜缺氧前后角膜荧光的变化,让2只眼睛接受100%的预湿氮气气流。将结果与相同受试者在相同条件下暴露于环境气流(氮气=69%;氧气=21%)后的结果进行比较。角膜荧光测量使用荧光光度计Flurotron Master FM2进行。

结果

作者发现,在正常条件下、缺氧条件下或气流条件下,这12名受试者的右眼和左眼之间的角膜荧光没有任何统计学上的显著差异(威尔科克森T检验、弗里德曼检验)。

结论

由于没有显著结果,这些作者认为,尽管在体外选择的暴露时间足以诱导细胞黄素蛋白荧光的改变,但在体内可能太“短”。使用FM2系统的互补滤光片会产生更多信息。对这些结果的研究促使作者扩大搜索范围,要么寻找全身缺氧的条件(低压舱),要么增加局部缺氧(隐形眼镜)。

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