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全氟戊烷(F4H5)对角膜内皮细胞的影响。

Effects of Perfluorobutylpentane (F4H5) on Corneal Endothelial Cells.

机构信息

a Department of Ophthalmology, University Medical Center Hamburg-Eppendorf (UKE) , Hamburg , Germany.

b Center of Ophthalmology, University Eye Hospital Tübingen , Tübingen , Germany.

出版信息

Curr Eye Res. 2019 Aug;44(8):823-831. doi: 10.1080/02713683.2019.1597891. Epub 2019 Apr 24.

Abstract

: To evaluate the effects of perfluorobutylpentane (F4H5) on corneal endothelial cell density (ECD) and morphology using a porcine corneal endothelial organ culture model. : "Split corneal buttons" were cultivated for 15 days (d) after incubation in F4H5 (15, 30, 60, and 120 min) or BSS (controls). ECD was assessed manually on d1, d8, and d15. After histological staining (trypan blue, alizarin red S) on d15 morphological changes (reformation figures, rosette formations, and alizarin red cells) were evaluated. : ECD was significantly reduced after incubation in F4H5 for 120 min (median ± 25%/75%-quartile; 3281 ± 43/222 cells/mm; = 0.046) on d15 compared to controls (3658 ± 129/296 cells/mm), but not after shorter incubation times (15, 30, and 60 min). Morphological assessment supports these findings as reformation figures (F4H5 120 min: 10.5 ± 9.3/13.9/mm vs. controls: 5.2 ± 2.8/7.2/mm; = 0.010), rosette formations (F4H5 120 min 25.566 ± 17.044/36.219/mm vs. controls: 8.333 ± 0.000/15.667/mm; = 0.002), and alizarin red cells (F4H5 120 min: 38.350 ± 29.827/51.333/mm vs. controls: 20.833 ± 10.417/25.000/mm; = 0.049) were significantly more prevalent after incubation in F4H5 for 120 min compared to controls. Also, F4H5 60 min showed significantly more rosette formations (25.452 ± 16.968/36.057/mm; = 0.006) and alizarin red cells (46.662 ± 42.420/50.903/mm; = 0.007), but not reformation figures (7.0 ± 2.2/1.6 %; = 0.953). : Short exposure (≤30 min) of porcine corneal endothelial cells to F4H5 does not have significant effects on ECD or morphological characteristics. Longer exposure times (≥60-120 min) may cause ECD decline and/or induce morphological changes.

摘要

目的

使用猪眼角膜内皮器官培养模型评估全氟戊烷(F4H5)对角膜内皮细胞密度(ECD)和形态的影响。

方法

将“角膜瓣”在 F4H5(15、30、60 和 120 分钟)或 BSS(对照)孵育后培养 15 天(d)。在 d1、d8 和 d15 手动评估 ECD。在 d15 进行组织学染色(台盼蓝、茜素红 S)后,评估形态变化(重构图形、玫瑰花结形成和茜素红细胞)。

结果

与对照组相比,F4H5 孵育 120 分钟后(中位数±25%/75%-四分位数;3281±43/222 个细胞/mm3; = 0.046),第 15 天 ECD 明显降低,但短时间孵育(15、30 和 60 分钟)则没有这种情况。形态评估支持这些发现,因为重构图形(F4H5 120 分钟:10.5±9.3/13.9/mm 与对照组:5.2±2.8/7.2/mm; = 0.010)、玫瑰花结形成(F4H5 120 分钟 25.566±17.044/36.219/mm 与对照组:8.333±0.000/15.667/mm; = 0.002)和茜素红细胞(F4H5 120 分钟:38.350±29.827/51.333/mm 与对照组:20.833±10.417/25.000/mm; = 0.049)在 F4H5 孵育 120 分钟后明显更常见。此外,F4H5 孵育 60 分钟时,玫瑰花结形成(25.452±16.968/36.057/mm; = 0.006)和茜素红细胞(46.662±42.420/50.903/mm; = 0.007)明显增多,但重构图形无明显变化(7.0±2.2/1.6%; = 0.953)。

结论

猪眼角膜内皮细胞短时间(≤30 分钟)接触 F4H5 不会对 ECD 或形态特征产生显著影响。较长时间(≥60-120 分钟)接触可能会导致 ECD 下降和/或诱导形态变化。

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