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人类玻璃体结构的年龄相关变化。

Age-related changes in human vitreous structure.

作者信息

Sebag J

出版信息

Graefes Arch Clin Exp Ophthalmol. 1987;225(2):89-93. doi: 10.1007/BF02160337.

Abstract

Changes in vitreous structure that occur with aging are important in the pathogenesis of vitreous liquefaction (synchisis senilis), vitreous detachment, and retinal disease. Vitreous morphology was studied in 59 human eyes post-mortem using dark-field horizontal slit illumination of the entire dissected vitreous. In many individuals younger than 30 years, the vitreous was homogeneous in structure. Middle-aged individuals had macroscopic fibers in the central vitreous, which coursed anteroposteriorly and inserted into the vitreous base and the vitreous cortex, posteriorly. During senescence, the vitreous volume was reduced, the vitreous body was collapsed (syneresis), and the fibers were thickened, tortuous, and surrounded by liquid vitreous. This sequence of age-related changes probably results from a progressive reorganization of the hyaluronic acid and collagen molecular networks. Characterization of the molecular events underlying these changes will elucidate the mechanisms of the phenomena of synchisis, syneresis, and detachment, and may provide methods with which to prevent or induce vitreous detachment prophylactically.

摘要

随着年龄增长而发生的玻璃体结构变化在玻璃体液化(老年性玻璃体皱缩)、玻璃体脱离及视网膜疾病的发病机制中具有重要意义。利用对整个解剖后的玻璃体进行暗场水平裂隙照明,对59只人眼的玻璃体形态进行了死后研究。在许多30岁以下的个体中,玻璃体结构均匀。中年个体的中央玻璃体有宏观纤维,这些纤维前后走行并插入玻璃体基部和后部的玻璃体皮质。在衰老过程中,玻璃体体积减小,玻璃体塌陷(脱水收缩),纤维增粗、扭曲并被液体玻璃体包围。这种与年龄相关的变化序列可能是由透明质酸和胶原分子网络的渐进性重组导致的。对这些变化背后分子事件的表征将阐明玻璃体皱缩、脱水收缩和脱离现象的机制,并可能提供预防性预防或诱导玻璃体脱离的方法。

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