首页> 美国卫生研究院文献>The British Journal of Ophthalmology >Effects of irrigation solutions on corneal endothelial function.
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Effects of irrigation solutions on corneal endothelial function.

机译:冲洗液对角膜内皮功能的影响。

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摘要

Rabbit corneas were perfused in vitro with an irrigation solution for 90 minutes. This was followed by 6 hours of perfusion with tissue culture medium TC199 during which endothelial function was assessed by monitoring rates of swelling during a period of perfusion in the absence of bicarbonate ions, and subsequent rates of thinning when bicarbonate ions were restored to the perfusate. Corneal thickness (measured with an ultrasonic pachymeter) immediately following excision was 401 microns (SD 19, n = 23). During the 90 minute perfusion at 35 degrees C, corneas exposed to balanced salt solution (BSS), Hartmann's solution or 0.9% NaCl (all initially at room temperature) swelled, respectively, at 14 (SD 2.3, n = 4), 11 (SD 2.6, n = 4), and 70 (SD 4.3, n = 4) microns/h. Cold Hartmann's solution (initially at 4 degrees C) caused corneas to swell at 9 (SD 2.3, n = 4) microns/h. On the other hand, corneas perfused with BSS Plus thinned at 9 (SD 3.4, n = 4) microns/h and TC199 with Earle's salts had little effect on thickness. Rates of swelling and thinning during the following assessment perfusion showed no apparent effects of prior exposure to any of the irrigation solutions on the barrier properties or pump function of the endothelium. Despite this, the increased thickness of corneas exposed initially to BSS, cold Hartmann's solution, or 0.9% NaCl was not fully reversed, even by the end of the 6 hour assessment perfusion. In contrast, the swelling observed in corneas exposed to Hartmann's solution at room temperature was reversed and these corneas had returned to their normal thickness by the end of the assessment period. All corneas, even those exposed to 0.9% NaCl, had an intact endothelial mosaic with no evidence of damage or cell loss, although morphological differences in cell shape and the appearance of cell borders were evident compared with freshly isolated cornea.
机译:在体外用冲洗液灌注兔角膜90分钟。随后用组织培养基TC199灌注6小时,在此期间通过监测在无碳酸氢根离子的情况下的灌注期间的溶胀率以及随后在碳酸氢根离子恢复为灌注液时变薄的速率来评估内皮功能。刚切除后的角膜厚度(用超声波测厚仪测量)为401微米(SD 19,n = 23)。在35°C的90分钟灌注过程中,暴露于平衡盐溶液(BSS),Hartmann溶液或0.9%NaCl(最初全部在室温下)的角膜分别在14(SD 2.3,n = 4),11( SD 2.6,n = 4)和70(SD 4.3,n = 4)微米/小时。冷哈特曼溶液(最初在4摄氏度)导致角膜以9(SD 2.3,n = 4)微米/小时的速度膨胀。另一方面,以9(SD 3.4,n = 4)micro / h稀释的BSS Plus灌注的角膜和含Earle盐的TC199对厚度的影响很小。在随后的评估灌注过程中,肿胀和变稀的速率表明,事先暴露于任何冲洗液中对内皮的屏障特性或泵浦功能均无明显影响。尽管如此,即使在6小时评估灌注结束时,最初暴露于BSS,冷Hartmann溶液或0.9%NaCl的角膜厚度仍未完全消除。相反,在室温下暴露于Hartmann溶液的角膜中观察到的肿胀得以逆转,并且在评估期结束时,这些角膜已恢复到正常厚度。所有角膜,即使是暴露于0.9%NaCl的角膜,都具有完整的内皮镶嵌,没有损伤或细胞丢失的迹象,尽管与新鲜分离的角膜相比,细胞形状和细胞边界的形态存在明显差异。

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