Suppr超能文献

组织的临床低温生物学:角膜的保存

Clinical cryobiology of tissues: preservation of corneas.

作者信息

Taylor M J

出版信息

Cryobiology. 1986 Aug;23(4):323-53. doi: 10.1016/0011-2240(86)90038-6.

Abstract

It is well recognized that the clarity of the cornea is a function of its hydration, and that this hydration is controlled by a "pump-and-leak" mechanism operating across the posterior monolayer of cells called the endothelium. A breakdown of the endothelium through disease or injury causes a marked increase in corneal thickness as the stroma imbibes fluid from the aqueous humor in the anterior chamber of the eye. This thickened, edematous condition of the stroma results in a cloudy cornea with an associated marked decrease in visual acuity. Treatment for this condition is usually by full-thickness corneal transplantation (penetrating keratoplasty), the success of which is dependent upon the donor cornea having an intact and healthy endothelium. It is essential, therefore, that any method of corneal storage for penetrating keratoplasty should protect and preserve the endothelium in a viable state. Current clinical practice relies upon short-term methods of preservation by two principal methods. Moist Chamber Storage is the time-honored corneal preservation method; it consists of keeping enucleated eyes at 0-4 degrees C in a sealed jar containing a pad of cotton gauze soaked in saline to provide a humid environment. The time limit placed upon this method of storage is 24-48 hr after which the viability of the endothelium deteriorates rapidly. Storage in M-K (McCarey-Kaufman) Medium involves excision of the corneoscleral segment from the donor eye and immersing it, endothelial side uppermost, in a medium consisting of tissue culture medium, 5% Dextran 40, and antibiotics. Laboratory and clinical studies indicate that storage in M-K medium at 4 degrees C preserves human endothelial cells for up to 4 days when the eye has been removed from the cadaver in less than 10 hr postmortem. Long-term preservation of corneas by freezing has long been a major goal in eye banking because indefinite storage by cryopreservation offers significant advantages for the quality and the quantity of material for use in keratoplasty, as well as for its distribution. However, procedures that have been developed for the cryopreservation of corneas have not been widely used, and a number of studies have shown that these procedures are inadequate for maintaining the integrity of the corneal endothelium. Not surprisingly, clinicians are now reluctant to accept corneas that have been frozen by these methods, though the clinical need is now greater than ever.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

人们普遍认识到,角膜的透明度取决于其水合作用,而这种水合作用是由一种“泵 - 漏”机制控制的,该机制通过称为内皮细胞的后单层细胞起作用。由于疾病或损伤导致内皮细胞受损,随着基质从前房房水中吸收液体,角膜厚度会显著增加。基质这种增厚、水肿的状态会导致角膜混浊,并伴有视力明显下降。这种情况的治疗通常采用全层角膜移植术(穿透性角膜移植术),其成功与否取决于供体角膜的内皮细胞是否完整健康。因此,对于穿透性角膜移植术而言,任何角膜储存方法都应将内皮细胞保护并维持在存活状态。目前的临床实践主要依靠两种短期保存方法。湿房保存是一种历史悠久的角膜保存方法;它包括将摘除的眼球置于0 - 4摄氏度的密封罐中,罐内有一块浸有盐水的纱布垫以提供潮湿环境。这种保存方法的时间限制为24 - 48小时,之后内皮细胞的活力会迅速下降。在M - K(麦凯里 - 考夫曼)培养基中保存涉及从供体眼中切除角膜巩膜段,并将其内皮面朝上浸入由组织培养基、5%右旋糖酐40和抗生素组成的培养基中。实验室和临床研究表明,当眼球在死后不到10小时从尸体上摘除时,在4摄氏度的M - K培养基中保存人内皮细胞可达4天。长期通过冷冻保存角膜一直是眼库的一个主要目标,因为通过冷冻保存进行无限期储存对于用于角膜移植的材料的质量和数量以及其分配都具有显著优势。然而,已开发的角膜冷冻保存程序尚未得到广泛应用,并且多项研究表明这些程序不足以维持角膜内皮细胞完整性。毫不奇怪,尽管临床需求比以往任何时候都大,但临床医生现在不愿接受通过这些方法冷冻的角膜。(摘要截取自400字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验